INDEX
Kanamycin I-123
actions of, 1148, 1159
adverse effects of, 1404
indications for, 1159
for MDR-TB, 1372, 1376, 1399
in pregnancy, 1152t
Kaolin-pectin, 1702t
Kaposi’s sarcoma
clinical features of, 397, 589f, 1581–1582, 1581f,
A5
diagnosis of, 1582
epidemiology of, 1556, 1565f
etiology of, 589, 1556
HHV-8 infection and, 712, 1491
in HIV infection, 1565f, 1581–1582, 1581f, 1582t
oropharyngeal, 260t
pathogenesis of, 1556
pericardial, 1568
staging of, 1582, 1582t
in transplant recipient, 1142, 1143, 1144
treatment of, 1582–1583, 1582t
Kaposi’s sarcoma-associated herpesvirus (KSHV)
infection. See Human herpesvirus-8
(HHV-8) infection
Kappa receptors, 3569t
Karnofsky Performance Scale, 485, 486t, 535
Karshi virus, 1626t
Karyomegalic tubulointerstitial nephritis, 2356,
2362
Karyorrhexis, 518
Katayama fever, 1786–1787
katG gene, 1360, 1375
KATs, 3792
Kava, 319, 472
Kawasaki’s disease
clinical features of, 137t, 142, 393
epidemiology of, 2816
inflammasome mutations in, 2678t
prognosis of, 2816
rash in, 137t, 393, A1
treatment of, 2816
vasculitis in, 2816
Kayser-Fleischer ring, 2549, 3236, 3236f, 3409, A15
KCl. See Potassium chloride (KCl)
KCNH2 gene mutations, 1925t
KCNJ2 gene mutations, 348
KCNJ5 gene mutations, 349
KCNJ18 gene mutations, 3530
KCNN4 gene mutations, 779t, 781
KCNQ1 gene mutations, 1925t
KCNQ2 gene mutations, 3308t
KDELR2 gene mutations, 3222t
KDM6A/B, 3794
KDPI (Kidney Donor Profile Index), 2325
Kearns-Sayre syndrome (KSS)
clinical features of, 3186, 3529, 3674t, 3675
AV conduction block, 1886
endocrine, 2970t, 2997
ocular, 227, 228
diagnosis of, 3529
genetic considerations in, 2970t, 3529
mtDNA mutation in, 2997, 3529, 3674t, 3675
treatment of, 3529
Kelley-Seegmiller syndrome, 3253
Kelling-Madlener procedure, 2451
Kell RBC group system, 887t, 888
Keloid, 370t, A5
Kemerovo virus, 1626t
Kennedy’s disease. See Spinobulbar muscular atrophy
Kenney-Caffey syndrome, 3186
Keratic precipitates, 220
Keratin, 2696t
Keratinocyte(s), 418
Keratinocyte growth factor therapy, 555
Keratitis, 220
A. baumannii, 1277
Acanthamoeba, 1719, 1719f
Aspergillus, 1679
Fusarium, 1689
HSV, 220, 1461t, 1462, 1474, 1478t
Nocardia, 1338, 1339t, 1340
Onchocerca, 1782
P. aeruginosa, 1287t, 1288
pigmented mold, 1688
Scedosporium, 1689
Keratoacanthoma, 586, 587f, A5
Keratoconjunctivitis, 220
Keratoconjunctivitis sicca (dry eye), 220
diagnosis of, 2788
differential diagnosis of, 2789t
in sarcoidosis, 2832
in Sjögren’s syndrome, 2788, 2789t
in systemic sclerosis, 2783
treatment of, 220, 2789
Keratoconus, 3227
Keratoderma blenorrhagica, 2798
Keratolytic agents, 382
Keratomalacia, 2530
Keratosis pilaris, 370t, 372f
Kerion, 380, 387t
Kerley B lines, 2007
Kernicterus, 2559, 2559t
Kernig’s sign, 1102
Kernohan-Woltman sign, 184
Keshan’s disease, 1965, 2534
Ketamine
abuse of, 180, 3576
antidepressant effects of, 3537–3538, 3544
overdosage/poisoning with, 3584
Ketoacidosis
alcoholic, 342, 362
breath odor in, 262
diabetic. See Diabetic ketoacidosis (DKA)
nausea and vomiting in, 292
treatment of, 366
α-Ketoadipic acidemia, 3270t
Ketoconazole
adverse effects of, 353, 380–381, 1703t, 2916,
3017
for candidiasis, 381
for Cushing’s disease, 2916
for Cushing’s syndrome, 2963
for cutaneous leishmaniasis, 1747
CYP3A and, 467t
drug interactions of
calcineurin inhibitors, 2328
CYP3A in, 467t, 2043
major, 1703t
PDE-5 inhibitors, 3060
proton pump inhibitors, 471t, 2444
sulfonylureas, 3111
tacrolimus, 2637
for ectopic ACTH syndrome, 724
for hypercalcemia, 357
for male precocious puberty, 3013
in pregnancy and lactation, 1703t
for seborrheic dermatitis, 377
shampoo, for tinea, 387t
Ketogenic diet, 3308t, 3317
Ketolides, 1149, 1159, 1164t, 1166–1167. See also
Telithromycin
Ketonuria, 3117
Ketoprofen, 3038
Ketorolac, 94, 95t, 220, 3634t
KFR (Kidney Failure Risk) equation, 2312
Khât, 3574, 3575. See also Psychostimulants
KI. See Potassium iodide (KI)
Ki67, 619, 2969
Ki67 proliferative index, 663, 664t, 673
Kidd RBC group system, 887t, 888
Kidney. See also Nephron(s)
calcium absorption/excretion by, 3160
congenital abnormalities of, 2356
disease/failure
acute. See Acute kidney injury (AKI)
chronic. See Chronic kidney disease (CKD)
glomerular. See Glomerular diseases
heart failure and, 1935
nephrolithiasis. See Nephrolithiasis
tubulointerstitial diseases. See
Tubulointerstitial diseases
vascular. See Renovascular disease
drug clearance in, 1150
embryological development of, 2287–2288, 2288f
erythropoietin production in, 431, 431f
in hypertension, 2072
in hypothermia, 3632t
phosphate absorption/excretion in, 3161
potassium absorption/excretion in, 349, 2291f,
2293–2294, S1
renin-secreting tumors of, 2074
sodium absorption/excretion in, 339f, 340, 340f,
2290–2291f, 2295–2296, 2295f, S1
uric acid metabolism in, 3249, 3250
vasculature of, 2088, 2288, 2289f
in vitamin D metabolism, 3166–3167, 3166f,
3167f
water absorption/excretion in, 339, 339f, 2290–
2291f, 2294–2295, 2295f, S1
Kidney biopsy. See Renal biopsy
Kidney cancer. See also Renal cell carcinoma (RCC)
deaths from, 481t, 484t, 673
hereditary papillary, 503t
incidence of, 481t, 484t, 673
infections in, 556t
paraneoplastic syndromes in, 722t, 725t
Kidney Donor Profile Index (KDPI), 2325
Kidney Failure Risk (KFR) equation, 2312
Kidney injury molecule-1 (KIM-1), 2305
Kidney mass, 2286–2287
Kidney transplantation, 2325
for acute intermittent porphyria, 3244
in diabetic nephropathy, 3124
donor selection for, 2325t, 2326–2327
for glucose-6-phosphatase deficiency, 3262
graft survival rates after, 2325, 2326t
HLA typing in, 2326
in lupus nephritis, 2748
mortality rates after, 2325, 2326t
organ allocation system for, 2325
presensitization in, 2326–2327
racial/ethnic disparities in referral for, 60, 61, 61f
recipient management
algorithm for, 2329, 2329f
chronic lesions of graft, 2330
complications, 2330–2331
induction therapy, 2327–2328
infections, 1141t, 1142–1143, 2330, 2330t
maintenance therapy, 2328–2329, 2328t
malignancy, 2330
in rejection, 2329–2330
recipient selection for, 2320, 2325–2326
rejection in, 2327, 2327f
results of, 2325, 2326t
in systemic sclerosis, 2786
tissue typing and immunogenetics in, 2326, 2327f
INDEX
I-124 Kikuchi’s disease, 1364
Killer cell immunoglobulin-like activating or
inhibitory receptors (KIRs), 2678, 2687t
Killian’s triangle, 2426, 2426f
KIM-1 (kidney injury molecule-1), 2305
Kimmelstiel-Wilson nodules, 2344, A4
Kimura’s disease, 1364
Kinase inhibitors, 512, 512f, 515, 2952. See also
specific drugs
Kinases, 511
Kindler syndrome, 386
Kingella kingae, 1247, 1247t. See also Infective
endocarditis, HACEK group
Kir 2.1 gene mutations, 3530
Kirby-Bauer method, S11
KIR gene, 1552t
KISS1 gene mutations, 2895, 3014, 3015t, 3032
KISS1R gene mutations, 3029, 3032
Kissing bug bite, 3615
Kisspeptin, 2888t, 2895, 2906, 3014, 3029
KIT gene mutations, 812, 812t, 864, 2729
KITLG gene mutations, 690
Kit ligand, 745
Kjer’s dominant optic atrophy, 218
Klebsiella spp., 1262, 1270
K. granulomatis. See Donovanosis
K. oxytoca, 1270
K. pneumoniae, 1165, 1168, 1262, 1270–1271,
1270f
Klebsiella spp. infections, 1270
abdominal, 1270f, 1271
bacteremia, 1271
in cancer patient, 558t
cellulitis, 1271
clinical features of, 300t, 977, 1270–1271
diagnosis of, 1270f, 1271
diarrhea, 300t, 1063
ecthyma gangrenosum, 399
epidemiology of, 1262
health care–associated, 969, 1131
liver abscess, 1059
pneumonia, 1271
rhinoscleroma, 1684
sepsis/septic shock, 2242
treatment of, 1157t, 1271
urinary tract, 1071, 1271, 2373
KLF1, 756
KLHL3, 353
Klinefelter syndrome, 2999
breast cancer in, 625–626
clinical features of, 2119, 2999, 3001t, 3010,
3016, 3018
diseases associated with, 2739, 3016
genetic considerations in, 3016
lymphoid malignancies in, 842t
mediastinal nonseminoma germ cell tumors in,
694
pathophysiology of, 2999
prevalence of, 2884t
screening/testing for, 2884t
treatment of, 2999–3000, 3016
Klippel-Trénaunay syndrome, 2116, 2119
KLLN gene mutations, 2984t, 2992
Kluyvera, 1275
KMT2A. See MLL
KMT2B gene mutations, 3402, 3403t
KMT2D gene mutations, 787
KMTs, 3792
Knee(s)
bursitis of, 2878
CPPD arthropathy of, 2865
gout tophi of, A15
iliotibial band syndrome in, 2879
osteoarthritis of, 2855, 2857, 2857f, 2859, 2859f
pain in, 2850, 2858, 2859f
Knee replacement, 2862
Knock-knees, 2850, 2857, 2857f
Knudson two-hit hypothesis/model, 3645t, 3651,
3655
Koebner (isomorphic) phenomenon, 377, 1581
KOH (potassium hydroxide) wet-mount
preparation, 372–373, S11
Koilonychia, 750
Kokobera virus, 1626t, 1631
Kommerell’s diverticulum, 2101
Koplik’s spots, 141, 392, 1610, A1. See also Measles
(rubeola)
Korsakoff ’s psychosis/syndrome, 2273, 3376, 3558
Kostmann’s syndrome, 444, 810
KPCs (Klebsiella pneumoniae, carbapenemaseproducing), 1165
Krabbe disease, 3256t, 3260, A16
Kraits, 3596. See also Snakebites
KRAS gene mutations
cancers associated with, 500, 500t
in carcinoma of unknown primary, 719
in cervical cancer, 698
in cholangiocarcinoma, 654
in colorectal cancer, 500t, 637
drug response and, 477t
as drug target, 515
liquid biopsy for detection of, 3838
in lung cancer, 596, 596f, 597t, 607
in multiple myeloma, 872
in ovarian cancer, 695
in pancreatic cancer, 658
in skin cancer, 419
syndromes associated with, 3650t
Kratom, 3786
Krukenberg tumors, 630, 695, 696
4Kscore Test, 683
KSHV (Kaposi’s sarcoma-associated herpesvirus)
infection. See Human herpesvirus-8
(HHV-8) infection
KSS. See Kearns-Sayre syndrome (KSS)
Ku-DNA-protein kinase, 2696t
Kugelberg-Welander disease, 3415
Ku-nucleoprotein La phosphoprotein, 2696t
Kupffer cells, 2547
Kurkino virus, 1628t
Kuru, 3417, 3417t
Kussmaul respiration, 187, 361, 3114
Kussmaul’s sign, 321, 1817, 1967, 2024
Kwashiorkor. See Malnutrition
Kyasanur Forest disease virus, 1626t, 1644
Kyphoplasty, 2908, 3199
Kyphoscoliosis, 124, 263, 265t
L
Labetalol
for aortic dissection, 2106
for hyperperfusion disorders, 2275
for hypertension, 2083t, 2084, 3356
for hypertension in pregnancy, 3763
for hypertensive emergencies, 2087, 2087t
for ischemic heart disease, 2040t
overdosage/poisoning with, 3591t
for preeclampsia, 3763
for sympathomimetic overdosage/poisoning, 3590t
Laboratory diagnosis/tests. See also Clinical
laboratory tests
infectious diseases, S11
parasitic infections, S12
Laboratory worker’s lung, 2160t
Labyrinthectomy, 241
Labyrinthine infarction, 241
Labyrinthitis, 80, 292, 293, 294t
Lacosamide, 702, 3318t, 3320, 3322f
Lacrimal glands, 220, 2837, 2838f
Lacrimation, with headache, 113
La Crosse virus, 1627t, 1637
Lactase deficiency, 2462
diagnosis of, 296, 306, 2463
diarrhea in, 303, 1064t
indigestion in, 295
pathophysiology of, 2462–2463
treatment of, 296, 303, 306, 2463
Lactate, arterial, 2246
Lactate dehydrogenase (LDH)
in ascitic fluid, 323
with left ventricular assist systems, 1976
in melanoma, 583
in non-Hodgkin’s lymphoma, 844
in PCP, 1692
in testicular cancer, 690, 693t
in thromboembolic renal disease, 2090
as tumor marker, 487t
Lactate dehydrogenase (LDH) deficiency,
3263t
Lactation. See Breast-feeding
Lactic acidosis
approach to the patient, 362
in cancer, 572
etiology of, 361–362
in malaria, 1724–1725
in shock, 2239
treatment of, 362, 366
Lactobacillus spp., 1083, 1085, 2447, 2492, 3296,
3699
Lactoferrin, 440, 443
Lactophenol cotton blue stain, S11
Lactose, 2460
Lactose breath hydrogen test, 306, 2463
Lactose intolerance/malabsorption. See Lactase
deficiency
Lactose tolerance test, 2463
Lactulose, 80, 80t, 303, 308, 2495, 2496t, 2633
Lacunar cells, A6
Lacunar infarction, 3326–3327, 3341, 3382, 3383f,
A16
LAD (leukocyte adhesion deficiency), 445, 446t,
2711, S8
LADs (lamin-associated domains), 3794
Lady Windermere syndrome, 1394
Lafora’s disease (progressive myoclonus epilepsy),
3308t, 3407
Laguna Negra virus, 1628t
Laherparepvec, 3690
Laing distal myopathy, 3525t, 3527
Lambert-Eaton myasthenic syndrome (LEMS)
vs. botulism, 1218
clinical features of, 3512–3513
diagnosis of, 3513
immunopathogenesis of, 2697t
in lung cancer, 599, 729, 3513
vs. myasthenia gravis, 3513
ocular manifestations of, 230
reflex responses in, 165
treatment of, 3513
LAMB syndrome. See Carney syndrome/complex
(LAMB/NAME syndrome)
Lamellar bone, 3159
Laminar-flow rooms, 564
Lamin-associated domains (LADs), 3794
Laminectomy, 122, 127, 129
Lamin proteins, 1955
INDEX
Lamivudine (3TC) I-125
adverse effects of, 1587t, 2596. See also specific
drugs
for chronic HBV infection, 1465t, 1466,
2595–2596, 2595t, 2599f, 2601, 2601t
for HBV prophylaxis in transplant recipient,
1145
for HIV infection, 1587t
molecular structure of, 1590f
in pregnancy, 2591
resistance to, 1466, 1592f, 2596, 2601t
Lamotrigine
adverse effects of
common, 3551t
cutaneous, 411, 3317
fever, 147
hypersensitivity, 412. See also Drug-induced
hypersensitivity syndrome (DIHS)
neurologic, 3318t
SJS or TEN, 392, 414, 3317, 3551t. See also
Stevens-Johnson syndrome (SJS); Toxic
epidermal necrolysis (TEN)
systemic, 3318t
contraindications to, 3317
drug interactions of, 3317, 3318t
for mood disorders, 3551, 3551t
overdosage/poisoning with, 3592t
pharmacology of, 3318t
for seizures, 702, 3318t, 3320
for SUNCT/SUNA prevention, 3367
for trigeminal neuralgia, 3438
LAMP2 deficiency (Danon disease), 1967, 3257t, 3267
LAMP2 gene mutations, 1956t, 1967, 3267
Lancinations, 168
Langerhans cell(s), 420
Langerhans cell histiocytosis (histiocytosis X), 257,
865, 2897, 2907, A12, A16
Langerhans cell sarcoma, 865
Language, 196, 3279, V2
Language barriers, 66
Laninamivir, 1464, 1512
Lanreotide
for acromegaly, 2913
adverse effects of, 2913
for gastrinoma, 2985
for gastrointestinal NETs, 636, 669, 669f, 671t
Lansoprazole, 296, 2443t, 2444, 2450, 2985
Lanthanum, 2314
Laparoscopic adjustable gastric banding, 3093f, 3094
Laparoscopic adrenalectomy, 2966
Laparoscopic appendectomy, 2516
Laparoscopic sleeve gastrectomy, 3093f, 3094
Laparoscopic ventral rectopexy (LVR), 2502, 2502f
Laparoscopy, 85, 112, 531, 1088
Laparotomy, 2508
Lapatinib
actions of, 513t, 544, 546t
adverse effects of, 546t, 739
for breast cancer, 544, 613t, 621, 625
genetic variations in response to, 477t
Laplace’s law, 1807
LA-PTT, 456
LARC/MIP-3α/Exodus-1, 2683t
Large granular lymphocytes, 425, 444. See also
Natural killer (NK) cells
Laron syndrome, 3735
Laron-type dwarfism, 2889, S8
Larotrectinib, 513t, 546t, 552, 607
Larva currens, 1775
Larva migrans
cutaneous
clinical features of, 1037, 1771
diagnosis of, S12
pathogenesis of, 1771
from pentastomes, 3611
treatment of, 1771t, 1772
ocular, 1771
visceral
clinical features of, 1699t, 1771, S6
diagnosis of, 1771, S6, S12
epidemiology of, 1771
incubation period for, S6
pathogenesis of, 1771
treatment of, 1708, 1771t, 1772, S6
in war veterans, S6
Laryngeal cancer, 591. See also Head and neck
cancer
Laryngeal nerve palsy, 3441–3442
Laryngitis, 255
Laryngotracheal stricture, 2828
Laryngotracheobronchitis (croup), 255, 1519
LAS (lung allocation score), 2209, 2211
Laser iridectomy, 221
Laser photocoagulation, 3122
Laser therapy
for basal cell carcinoma, 588
for hair removal, 3042
for warts, 1503, 1503t
LASIK, 216
Lasmiditan, 3362t, 3363t, 3364
Lassa fever, 978, 1642
Lassa virus, 1626t
Latency-associated transcripts (LATs), of HSV,
1471
Lateral epicondylitis, 2879–2880
Lateral femoral cutaneous neuropathy (meralgia
paresthetica), 3498, 3767
Lateral geniculate body, 215
Lateral inferior pontine stroke syndrome, 3330f
Lateral medullary stroke syndrome, 3329f, 3331,
A16
Lateral midpontine stroke syndrome, 3331f
Lateral sclerosis, 3410, 3454
Laterocollis, 3402
Latex agglutination assay, S11
α-Latrotoxin, 3612
LATs (latency-associated transcripts), of HSV,
1471
Latvia, 43t
Laugier-Hunziker syndrome, 390
Laurence-Moon syndrome, 3016
Laxatives
abuse of, 303, 304, 349
adverse effects of, 301, 302, 349
for constipation, 79, 80t, 307, 308
for IBS, 2495
for internal radionuclide contamination, S5
LCAT deficiency, familial, 2906, 3139t
LCIS (lobular carcinoma or neoplasia in situ),
617
LCK-TCRB gene mutations, 500t
LCM (lymphocytic choriomeningitis), 1106, 1108,
1114t, 1626t, 1639
LCZ696. See Sacubitril-valsartan
LDH. See Lactate dehydrogenase (LDH)
LDL-C. See Low-density lipoprotein cholesterol
(LDL-C)
LDLRAP1 gene mutations, 3141
LDLR gene mutations, 3140
Lead oxide exposure, 3581
Lead poisoning
vs. ALS, 3412
clinical features of, 3377, 3579, 3580t
diagnosis of, 3495, 3580t
hemolytic anemia in, 788
hypertension and, 3579
metabolism of, 3580t
neuropathy in, 3493, 3495
optic neuropathy in, 224
oral manifestations of, 260t
peripheral blood smear in, 425, 429f
pregnancy-associated risks, 3579
sources of, 3580t
treatment of, 3377, 3495, 3580t
Lead-time bias, 38, 494, 597
Leaky epithelia, 2289
Leber’s hereditary optic neuropathy (congenital
amaurosis)
clinical features of, 223, 2351t, 3673, 3674t
diagnosis of, 3673, 3676
gene therapy for, 3688
genetic considerations in, 223, 2351t
genetic counseling in, 3678
mtDNA mutation in, 3673, 3674t, 3676
treatment of, 223, 227, 3678
visual fields in, 218
Lebombo virus, 1626t
Lechiguanas virus, 1628t
Lectins, 744
Ledipasvir/sofosbuvir, 1467, 1468t, 2607,
2608t
Leeches, 1248
Leech infestations, 3611–3612
Lefamulin
actions of, 1149, 1161, 1164t, 1165f
adverse effects of, 1154t, 1161
drug interactions of, 1155t, 1161
indications for, 1157t, 1161, 1167
in pregnancy and lactation, 1152t
resistance to, 1157t, 1164t, 1165f, 1167
Leflunomide
adverse effects of, 2762t, 3494t
monitoring during treatment with, 2762t
for psoriatic arthritis, 2800
pyrimidine metabolism and, 3254
for rheumatoid arthritis, 2761, 2762t,
2764
for SLE, 2747
Left atrial appendage closure, A11
Left bundle branch, 1880
Left bundle branch block, 1821f, 1827–1828, 1827f,
1935, A7, A8
Left ventricular aneurysm, 2064–2065
Left ventricular assist systems, 1144, 1975–1977,
1976f, 1977f. See also Mechanical
circulatory support
Left ventricular dysfunction
in aortic regurgitation, 1987
cardiogenic shock in, 2250
diagnosis of, 1838, 1839f, 1859v, 1863–1864,
1863f
in heart failure. See Heart failure (HF)
in mitral regurgitation, 1996
pulmonary hypertension and, 2126
in STEMI, 2061–2062
Left ventricular hypertrophy
in CKD, 2315
ECG in, 1827, 1827f, A7
hypertension and, 2075, A7
with myocardial ischemia, 2031
Left ventricular noncompaction, 1956t, 1966
Left ventricular pressure-volume relationship, 1809,
1809f
Left ventricular remodeling, 1933, 1934t,
2061–2062. See also Heart failure (HF)
Legal blindness, 216
INDEX
I-126 Legal issues
advance care planning, 77
euthanasia and physician-assisted suicide, 87
incompetent patient, 68
mandated reporting, 68
Leg elevation, for stasis dermatitis/ulceration, 377,
385t
Legionella spp.
apoptosis inhibition by, 957
cellular trafficking of, 953
epigenetic modulation by, 958
laboratory identification of, S11
microbiology of, 1250
Naegleria and, 1718
NF-κβ inhibition by, 956
non-pneumophilia, 1250
secretion system of, 952
in water systems, 1250–1252, 1251f, 1252t,
1256–1257
Legionella spp. infections, 1249
in cancer patient, 481, 561t, 1252
clinical presentation of, 1253, 1253t
diagnosis of, 1012, 1253–1255, 1254f, 1255f, S11
epidemiology of, 1250, 1251f
common-source outbreaks, 1134, 1250–1252,
1251f, 1252t, 1257
seasonality and climate in, 1250
sporadic outbreaks, 1252
transmission, 1252–1253
non-pneumophilia, 1253, 1254, 1255f
prevention of, 1256–1257
prognosis of, 1256
in renal transplant recipient, 1142
risk factors for, 1011, 1252
treatment of, 1255–1256, 1256t
Legionnaire’s disease. See Legionella spp.
infections
Leigh’s syndrome, 3529, 3674t, 3675, 3678, A16
Leiomyoma (uterine fibroids), 636, 699, 2398f,
3037, 3038, 3052–3053
Leiomyomatosis, hereditary, 674t
Leiomyosarcoma, 699, 700, 713. See also Soft tissue
sarcomas
Leishmania spp., 1698
characteristics of, 1742, 1742t
entry into host, 2694
geographic distribution of, 1742t
laboratory identification of, S12
L. aethiopica, 1742t, 1746
L. braziliensis, 1742t, 1746, 1747, S12
L. donovani, 1742t, S12. See also Visceral
leishmaniasis
L. guyanensis, 1747
life-cycle hosts of, S12
life cycle of, 1741–1742, 1742t
L. infantum, 1742t, 1743
L. major, 1742t, 1746, 1747
L. mexicana, 1742t, 1746, 1747
L. tropica, 1742t, 1746, S12
Leishmania spp. infections, 1741
cutaneous. See Cutaneous leishmaniasis
diffuse cutaneous, 1742t, 1747
epidemiology of, 1742–1743, 1742t, 1743f, S6,
S12
mucosal, 1742t, 1747–1748, 1748f
prevention of, 1748
visceral. See Visceral leishmaniasis
Lemborexant, 212
Lemierre’s disease/syndrome, 254, 979, 1020–1021,
1351
LEMS. See Lambert-Eaton myasthenic syndrome
(LEMS)
Lenalidomide
actions and targets of, 536f, 537
for adult T-cell leukemia/lymphoma, 1526
adverse effects of, 740, 742, 802, 875
for amyloidosis, 882
for DLBCL, 847
for follicular lymphoma, 848
for gastric lymphoma, 634
for MDS/MPY with ring sideroblasts, 862
for multiple myeloma, 873–875, 874t
for myelodysplasia, 801–802
for POEMS syndrome, 2996
for primary effusion lymphoma, 857
Lenègre disease, 1881
Length bias, 38
Length-biased sampling, 494, 597
Lennox-Gastaut syndrome, 3307
Lenticulostriate arteries, 3325
Lentigo, 390
Lentigo maligna, 581t, 582f, 583, A5
Lentiviruses. See also HIV
in gene therapy, 3299, 3685t, 3687
nononcogenic, 1527
phylogenetic tree of, 1528f
structure and life cycle, 1523
Lenvatinib
action and targets of, 513t, 526, 547t
adverse effects of, 547t, 653, 739
for endometrial cancer, 700
for hepatocellular carcinoma, 649, 649t, 651f,
652–653, 652f
for renal cell carcinoma, 511, 648, 649, 676t
LEOPARD syndrome, 390
LEP gene mutations, 3015t
Lepirudin, 932, 933t
Lepra cells, 1382
LEPR gene mutations, 3015t
Lepromatous leprosy, 1037, 1383, 1386–1387,
1386f, A5
Lepromin test, 1388
Leprosy, 1382
clinical features of, 1037, 1385, S6
borderline lepromatous, 1386, 1386f
borderline tuberculoid, 1385, 1385f
lepromatous, 1037, 1383, 1386–1387, 1386f,
A5
neuropathy, 3440, 3490
renal, 71, 2336t
tuberculoid, 389–390, 1385, 1385f
complications of, 1387
diagnosis of, 1388–1389
differential diagnosis of, 1388
epidemiology of, 1383–1384, 1383f, 1384f
etiology of, 1382–1383
global considerations in, 1383–1384, 1384f,
1385f, 3490
incubation period for, 1384, S6
indeterminate, 1385
inflammasome mutations in, 2677t
lepromatous, 3490
multibacillary, 1389, 1389t
pathogenesis of, 1384–1385
paucibacillary, 1389, 1389t
postexposure prophylaxis for, 1392
prevention and control of, 1392
primary neuritic, 1387
rehabilitation and social aspects,
1391–1392
Ridley-Jopling classification of, 1384–1385
transmission of, 1384
treatment of, 3490, S6
adverse effects of, 1389
disease management during and after,
1390–1391
leprosy reactions, 1390
multidrug, 1389, 1389t
nerve function impairment and neuropathic
pain, 1390
relapse, 1389–1390
second-line drugs, 1390
tuberculoid, 3490
vaccines, 1392
WHO classification of, 1385
Leprosy reactions, 1387, 1387f, 1390
Leptin
actions of, 3081, 3808
deficiency of, 2897
in hypogonadotropic hypogonadism, 3014, 3035
in male pubertal development, 2906
in obesity, 3083, 3084t
resistance to, 3151
Leptin receptors, 3084–3085, 3084t
Leptomeningeal metastases, 709–710, 709f, S2
Leptospira/leptospirosis (Weil’s syndrome), 1417
clinical features of, 135t, 141, 320, 1113t,
1419–1420
diagnosis of, 964, 1420, S6, S11
differential diagnosis of, 1420–1421
epidemiology of, 1417–1418
etiologic agent of, 1417, 1417f, 1418f
global considerations in, 1418
incubation period for, 1418f, 1419, S6
in international travelers, 1418
pathogenesis of, 1418–1419, 1418f, 1419f
prevention of, 1421, 1421t, S6
prognosis of, 1421
treatment of, 1421, 1421t, S6
Leriche’s syndrome, 2106
LERPE1 gene mutations, 3222t
LES (lower esophageal sphincter), 288, 2427,
2428f
Lesbian, 3079t
Lesbian, gay, bisexual, and transgender (LGBT)
patients, 3078
Lesch-Nyhan syndrome, 3253
Leser-Trelat sign, 390
Letermovir, 1462, 1490
Lethal midline granuloma. See Extranodal NK/
T-cell lymphoma, nasal type
Letrozole, 543, 573, 613t, 620, 3037, 3052
Leucine metabolism disorders, 3270t
Leucovorin
for colorectal cancer, 642–643
for DLBCL, 847
5-FU and, 542
for gastric cancer, 633
methotrexate and, 541t, 542
for osteosarcoma, 715
for pancreatic cancer, 662
for PCP prophylaxis, 1563t, 1695t
for toxoplasmosis prophylaxis, 1563t
Leukapheresis, for CML, 827
Leukemia
acute lymphoid. See Acute lymphoid leukemia
(ALL)
acute myeloid. See Acute myeloid leukemia
(AML)
acute promyelocytic. See Acute promyelocytic
leukemia (APL)
adult T cell. See Adult T-cell leukemia/
lymphoma
aggressive NK cell, 858
chemotherapy-associated, 854
chromosome abnormalities in, 516–517
INDEX
chronic eosinophilic, 803, 863, 863t I-127
chronic lymphocytic. See Chronic lymphocytic
leukemia (CLL)
chronic myeloid. See Chronic myeloid leukemia
(CML)
chronic myelomonocytic, 799, 860–861, 860t
chronic neutrophilic, 803, 859, 860t
deaths from, 481t, 483f, 484t
definition of, 508
gene therapy for, 3689
hairy cell. See Hairy cell leukemia
incidence of, 481t
infections in, 558
joint involvement in, 2877
juvenile myelomonocytic, 861–862
late consequences of treatment, 741
lymphadenopathy in, 458
mast cell, 2729
neuropathy in, 3491
ocular invasion by, 227
oral manifestations of, 257
paraneoplastic syndromes in, 725t
polycythemia vera and, 804
splenomegaly in, 461
T-cell large granular lymphocytic, 857–858, 2753
T-cell prolymphocytic, 463, 857
viruses and, 505
Leukemia cutis, 396
Leukemia inhibitory factor (LIF), 2683t
Leukemoid reaction, 445
Leukoaraiosis (diffuse/periventricular white matter
disease), 193f, 3343
Leukocyte(s), 425, A4. See also Basophil(s);
Eosinophil(s); Lymphocyte(s);
Monocyte(s); Neutrophil(s)
Leukocyte adhesion deficiency (LAD), 445, 446t,
2711, S8
Leukocyte common antigen, 718t
Leukocyte esterase test, 1075
Leukocyte function-associated antigen (LFA-1),
2696t
Leukocytoclastic (cutaneous small-vessel) vasculitis
clinical features of, 140t, 144, 399, A1, A5
drug-induced, 414–415, 414f
epidemiology of, 140t
etiology of, 140t, 399
Leukoderma, 387–389, 389t
Leukodystrophy(ies), 3256t, 3377
Leukoencephalopathy
methotrexate-related, 742
progressive multifocal. See Progressive multifocal
leukoencephalopathy (PML)
radiation therapy–related, 711
reversible posterior, 571, 3343, 3350–3351
Leukoerythroblastosis, 802. See also Primary
myelofibrosis
Leukopenia. See Neutropenia
Leukoplakia, 372f
hairy, 260t, A5
oral
characteristics of, 257, 372f, A3
in dyskeratosis congenita, 3681, 3682f
etiology of, 257
as premalignant lesion, 492, 590, 591
smoker’s, 260t
sublingual, A3
Leukostasis, 571
Leukotriene modifiers, 2156–2157, 2158, 2158t. See
also Montelukast; Zafirlukast
Leukotrienes, 91f, 408
Leuprolide, 544, 613t, 620, 686, 2747
Levamisole, 410, 905t, 2807, 2847t, 3575
Levetiracetam
adverse effects of, 3317, 3319t
for cyclic vomiting syndrome, 294, 294t
for myoclonus, 3407
overdosage/poisoning with, 3592t
for seizures, 571, 702, 3319t, 3320
for status epilepticus, 3322f
Levine’s sign, 105, 2033
Levodopa
actions of, 3393, 3394f
adverse effects of, 2527, 3393–3394, 3399
for dystonia, 3403–3404
for PD, 3392–3394, 3394f, 3396t, 3399
Levofloxacin
actions of, 1149, 1160, 1164t
adverse effects of, 2584
for Campylobacter infections, 1304
for community-acquired pneumonia, 947t, 1014t
for C. trachomatis infection, 1450
for epididymitis, 1082
for HACEK endocarditis, 1247, 1247t
for hospital-acquired pneumonia, 947t, 1018t
in H. pylori eradication, 1283t, 2446–2447, 2447t
indications for, 1157t, 1160
for infections in cancer patient, 563
for infectious diarrhea, 1065t
for intraabdominal infections, 947t
for Legionella spp. infections, 1256t
for leprosy, 1390
for MDR-TB, 1372, 1376–1377, 1376t, 1399t, 1402
for nongonococcal bacterial arthritis, 1042
for osteomyelitis, 1049t, 1050t
for P. aeruginosa infections, 1287t
for peritonitis, 1056
for plague, 1324, 1324t, S3
for plague prophylaxis, 1325, 1325t
for pneumococcal infections, 1176
prophylactic, 901t, 1162t
resistance to, 1013, 1157t, 1164t, 1283
for sepsis/septic shock, 2248t
for sinusitis, 252
for tularemia prophylaxis, 1319t
for ventilator-associated pneumonia, 1018t
Levomilnacipran, 3542t, 3549
Levonorgestrel, 3054, 3055
Levorphanol, 95t, 98
Levosimendan, 1945, 1946t, 1953
Levothyroxine (LT4)
adverse effects of, 2936
for diffuse nontoxic goiter, 2946
drug interactions of, 2937
for hypothyroidism, 2936–2937
for myxedema coma, 2937
in older adults, 2937
in pregnancy, 2937
for subacute thyroiditis, 2944
Lev’s disease, 1881
Lewisite, S4
Lewis RBC group system, 887t
Lewis-Sumner syndrome, 3504
Lewy body(ies)
characteristics of, 3297, 3385
dementia with. See Dementia with Lewy
bodies
in PD, 3387, 3387f
prions and, 3297f, 3422
proteostasis loss and, 3734, 3735f
Leydig cell, 2906, 2907f
LFA-1 (leukocyte function-associated antigen),
2696t
LGBT (lesbian, gay, bisexual, and transgender)
patients, 3078
LGI1 antibodies, 729t, 731f, 733
LGI1 gene mutations, 3308t
LGV. See Lymphogranuloma venereum (LGV)
LH. See Luteinizing hormone (LH)
LHCRG gene mutations, 3003t
Lhermitte’s sign/symptom
in cervical spine lesions, 127, 128, 172, 3277
in MS, 3277, 3463
radiation therapy–related, 741, 854
in spinal cord compression, 568
LHON. See Leber’s hereditary optic neuropathy
(congenital amaurosis)
LHX3 gene mutations, 3014, 3015t
LHβ gene mutations, 3014, 3015t
Lialda, 2483, 2483t
Libertarian paternalism, 3775
Libido
female, 3062
in hypothyroidism, 2935
in malabsorption disorders, 2468t
male, 3055
Libman-Sacks endocarditis, 2742, 2743
Lice
body (Pediculus humanus), 1422, 1435,
3610–3611
diseases carried by
epidemic typhus. See Epidemic (louse-borne)
typhus
relapsing fever. See Relapsing fever
head (Pediculus capitis), 3610–3611
Lichen amyloidosis, 395
Lichenification, 374, 374f
Lichen myxedematosus, generalized (papular
mucinosis), 395
Lichenoid lesions, 370t
Lichen planopilaris, 379
Lichen planus, 378
clinical features of, 377t
alopecia, 384
distribution, 370t, 372f, 379
esophageal, 290
morphology, 370t
oral manifestations, 257, 259t, 260t, A3
papules and plaques, 379, 379f, A5
papulosquamous lesions, 383
in diabetes mellitus, 3128
drug-related, 379
erosive, A3
HCV infection and, 379, 383, 2604
histologic features of, 377t
treatment of, 379
Lichen simplex chronicus, 372f, 375
Lichen tropicus, 3636
Licorice, 349, 350, S1
Liddle’s syndrome (pseudoaldosteronism)
clinical features of, 349, 366, 2080t, 2294
diagnosis of, 350, 2964
genetic considerations in, 349–350, 2080t, 2292t,
2964, 2965t
pathogenesis of, 366
pathophysiology of, 2080, 2294
treatment of, 350, 367, 2967
Lidocaine
for arrhythmias, 1872t, 1913
for cardiac arrest due to VT or VF, 2262f, 2263
for IC/BPS, 330
inhaled, for cough, 270
metabolism of, 467t
for neuropathy, 98, 3488t
for SUNCT/SUNA, 3367
for topical anesthesia in lumbar puncture,
S9
INDEX
I-128 Lidoderm patch, 3488t
LIF (leukemia inhibitory factor), 2683t
Life expectancy
at birth by county, U.S., 61f
genetic considerations in, 3677
global burden of disease and, 3704
global differences in, 3719, 3720f, 3721f
by race and sex, U.S., 60f
screening procedures and increase in, 38t
of women, 3063–3064
Lifestyle modifications
for GERD, 2430–2431
for hypertension, 2082, 2082t
for metabolic syndrome, 3155
for NAFLD, 2622
for obesity, 3089–3091
Li-Fraumeni syndrome
breast cancer screening in, 615
clinical features of, 703t, 712
genetic considerations in, 503t, 509, 595, 703t,
712, 3645t, 3664
lung cancer risk in, 595
Light chain deposition disease/nephropathy
clinical features of, 2335t, 2345, 2360
diagnosis of, 2360
etiology of, 2360
pathophysiology of, 2360
in POEMS syndrome, 2367
renal biopsy in, 2360f, A4
treatment of, 2345, 2360
Light-headedness, 159
Likelihood ratio, 25, 26f
Lille score, 2619
LILRB2 gene, 1552t
Limaprost, 3635
Limb apraxia, 198
Limb dystonia, 3402
Limb-girdle muscular dystrophies (LGMDs)
autosomal dominant, 3522t
autosomal recessive, 3523–3524t
classification of, 3521–3522
clinical features of, 3521
diagnosis of, 3521
genetic considerations in, 3650, 3650t
global considerations in, 3532
prevalence of, 3522
proteins involved in, 3526f
Limbic encephalitis, 729, 731f, 3377, A16
Limbic network/system, 202
Limb ischemia, 2110–2111. See also Peripheral
artery disease
Limb-kinetic apraxia, 198
Limb-sparing surgery, 713, 715
Limey bile, 2648
Limit dextrinosis (type IIIa/b GSD), 1967, 3262,
3263t
Linaclotide, 307, 308, 2495, 2496t
Lincosamides. See Clindamycin
Lindane, 3608, 3611
Linear IgA disease, 401t, 404, 409
Linear nevoid hypopigmentation (hypomelanosis
of Ito), 389
Linear scleroderma, 384
Linezolid
actions of, 1149, 1164t, 1187, 1403
adverse effects of, 905t, 1154t, 1160–1161, 1187,
1202, 1377, 1398t, 1403
for community-acquired pneumonia, 947t, 1014t
drug interactions of, 1155t, 1161, 1403
for enterococcal infections, 1201t, 1202
indications for, 1157t, 1160
for MDR-TB, 1372, 1376–1377, 1376t, 1403
for MRSA infections, 947t, 1015, 1018, 1186t,
1187
for Nocardia infections, 1336t, 1339
for NTM infections, 1406
for osteomyelitis, 1050t
for peritonitis, 1056
in pregnancy and lactation, 1152t
resistance to, 1157t, 1164t, 1167, 1187, 1203
for staphylococcal infections, 1039t, 1187
for TB, 1398t, 1403
for toxic shock syndrome, 1188
for ventilator-associated pneumonia, 1018, 1018t
LINGO-1, 3293
Linifanib, 652f
Linkage analysis, 3655–3656, 3659t
Linkage disequilibrium, 3657, 3659t
Linoleic acid, 2521t
α-Linolenic acid, 2521t
Lionfish sting, 3604
Liothyronine, 2937, 2952
LIPA gene mutations, 3260
LipA lipase, 1276
Lipase, 2653, 2654t, 2668
LIPC gene mutations, 3143
Lipedema, 2120
Lipemia retinalis, 3138
Lipid(s)
defects in metabolism of, 3528
deposits of, in familial hypercholesterolemia,
A15
digestion and absorption of, 2459–2460, 2460f,
2460t
as energy source, 3528
neutral, disorders of, 3257t
in parenteral nutrition, 2542, 2544
production of, 3101
transport of, 3135–3136, 3137f
Lipid mediator generation, 2720, 2720f
Lipid membrane microdomain (lipid raft), 2691
Lipid nanoparticles, 3685, 3685t
Lipoarabinomannan, 1360, 1382
Lipoatrophy, 3128
Lipodermatosclerosis, 397, 2116
Lipodystrophy
in diabetes mellitus, 3119
familial, 3138–3140, 3151, 3649, 3650t
forms of, A15
in HIV infection, 1572, 1572f, 1586, 3119, 3151
metabolic syndrome and, 3151
protease inhibitors and, 3119
treatment of, 3139–3140
Lipofuscin, 3734, 3735f
Lipoglycopeptides, 1148, 1158–1159, 1164t, 1166
Lipohypertrophy, 3128
Lipoic acid, 237, 261
Lipoidal tests, for syphilis, 1410–1411
Lipolysis, 2460, 2460f
Lipolytic enzymes, 2657
Lipomas, 395, 636, 2027, 2984t, 2988
Lipooligosaccharide (LOS), N. gonorrhoeae,
1235
Lipopeptides. See Daptomycin
Lipopolysaccharide (LPS)
B. cepacia, 1290
Brucella, 1311–1312
epigenetics of, 3795
in heart failure, 1935
P. aeruginosa, 1285, 1285t
in sepsis/septic shock, 1262, 2243
Lipoprotein(a), 3136, 3136t, 3137–3138, 3140t
Lipoprotein(s)
classification of, 3135, 3136f
composition of, 3135. See also High-density
lipoprotein cholesterol (HDL-C); Lowdensity lipoprotein cholesterol (LDL-C);
Very low–density lipoproteins (VLDLs)
metabolism of, 3135, A10
in nutrition assessment, 2538t
proteins associated with, 3135
in transport of dietary lipids, 3135–3136, 3137f
Lipoprotein disorders
approach to the patient, 3147
arthritis in, 2873
cardiovascular disease risk and, 1814, 2040
in diabetes mellitus, 3126–3127
diagnosis of, 3147
with elevated apoB-containing lipoproteins,
3138
hypercholesterolemia. See
Hypercholesterolemia
hypertriglyceridemia. See
Hypertriglyceridemia
mixed hyperlipidemia. See Mixed
hyperlipidemia
erectile dysfunction in, 3057
global considerations in, 1814
with low HDL-C. See High-density lipoprotein
cholesterol (HDL-C), low levels of
with low LDL-C. See Low-density lipoprotein
cholesterol (LDL-C), low levels of
musculoskeletal disorders associated with, 2873
in obesity, 3086
screening for, 39t, 2883t, 3137–3138, S10
secondary causes of, 2658–2659, 2663
skin manifestations of, 395
Lipoprotein glomerulopathy, 2347
Lipoprotein lipase (LPL)
in hypertriglyceridemia, 3138
in hypolipidemia, 3146
in insulin resistance, 3151
in lipoprotein metabolism, 3135–3136, 3137f
in metabolic syndrome, 3144
Lipoprotein lipase (LPL) deficiency, 3138, 3688
Liposarcoma, 713. See also Soft tissue sarcomas
Lip reading, 247
Liquid biopsy, 3836, 3837f. See also Cell-free DNA
(cfDNA); Circulating tumor DNA (ctDNA)
Liquid chromatography, 3833
Liquid nitrogen therapy, 381
Liraglutide, 2623, 3092–3093, 3092t, 3110t, 3111,
3155
Lisch nodules, 2980, 2990
Lisdexamfetamine, 3474
Lisfranc fracture–dislocation, 2874
Lisinopril, 1948t, 2083t
Lispro, 3108, 3108t
Lissencephaly, 3300, 3308t
Listeria monocytogenes
autophagy evasion by, 958
characteristics of, 1208
epigenetic modulation by, 958
genome sequencing of, 972
laboratory identification of, S11
survival in vacuole, 953
Listeria monocytogenes infections, 1208
bacteremia, 1210
in cancer patient, 556t, 558t
diagnosis of, 1210
epidemiology of, 1209–1210
food-related, 301, 1209–1210, 1209f
immune response to, 1209
meningitis, 978, 1101, 1104t, 1105, 1210
neonatal, 1210
neurologic, 1210
INDEX
pathogenesis of, 1208–1209 I-129
in pregnancy, 1210
prevention of, 1211
in transplant recipient, 1141t, 1143, 1144
treatment of, 1211
Listeriolysin O (LLO), 953, 1209
Lithium
actions of, 3537–3538
adverse effects of
acid-base disorders, 360
alopecia, 384
common, 3551, 3551t
cutaneous, 382, 383, 386, 409
hypercalcemia, 3178
lupus syndrome, 2847t
nail disorders, 410
nephrogenic diabetes insipidus, 346, S1
nephropathy, 2362–2363
neuropathy, 3494t
nystagmus, 231
psoriasis, 377
rare, 3551t
SA node dysfunction, 1875t
secondary parkinsonism, 3389
seizures, 3311t
weight gain, 3087
for bipolar disorder, 3551, 3551t
for cluster headache prevention, 3367, 3367t
drug interactions of, 1705t
for hypnic headache, 3369
overdosage/poisoning with, 3595t
pharmacology of, 3551t
Livedo reticularis, 88, 399, 2113f, 2114, 2750
Liver
alcohol effects on. See Alcohol-associated liver
disease
anatomy of, 2546–2547, A13
drug metabolism in, 466–467
drug transport in, 466, 466f
functions of, 2547
palpation of, 322
Liver abscess, 1058
in actinomycosis, 1342, 1342f
amebic
clinical features of, 1716, S6
complications of, 1717
diagnosis of, 1059, 1717, 1717f, S12
epidemiology of, 1716
pathogenesis of, 1698, 1716
treatment of, 1718, 1718t, S6
Candida, 1059
clinical features of, 1058–1059
diagnosis of, 1059, 1059f
etiology of, 1058
K. pneumoniae, 1059, 1270f, 1271
treatment of, 1059
Liver biopsy, 2551, A13
in acetaminophen hepatotoxicity and alcoholic
liver injury, A13
in acute hepatitis, A13
in alcohol-associated liver disease, 2618
in α1
-antitrypsin deficiency, A13
in autoimmune hepatitis, 2615, A13
in chronic HBV infection, A13
in chronic HCV infection, 2600, 2604, A13
in cirrhosis, A13
in cirrhosis secondary to hemochromatosis with
hepatocellular carcinoma, A13
in CMV infection with liver allograft, A13
contraindications to, 2556
in hemochromatosis, 3234, A13
in hepatic granuloma, A13
in hepatocellular carcinoma, 647, A13
indications for, 2554f, 2556
in NAFLD, 2621–2622
in nonalcoholic steatohepatitis, A13
in primary biliary cholangitis, A13
in primary sclerosing cholangitis, A13
in rejection of liver allograft, A13
in Wilson’s disease, 3236, A13
Liver disease/failure, 2547. See also Cirrhosis
in alcohol abuse. See Alcohol-associated liver
disease
in α1
-antitrypsin deficiency, 2549
in β thalassemia, 763t
in cancer patient, 560, 742
cholestatic, 319–320, 2427, 2547, 2547t. See also
Biliary cirrhosis
clinical features of, 321, 2547
anemia, 753–754
ascites, 322f, 323, 2549
bleeding, 454
coagulation disorders, 917–918, 918f, 918t
cutaneous, 2549
dyslipidemia, 3144–3145
encephalopathy. See Encephalopathy, hepatic
fatigue, 2548
halitosis, 262
hepatomegaly, 2549
icterus, 2549
itching, 2548
jaundice, 318–319, 2548
lactic acidosis, 361
nausea and vomiting, 292, 2548
neuropathy, 3490
oral, 257
pain, 2548
respiratory, 368
splenomegaly, 2549
thromboembolism, 918, 918f
clinical history, 2547–2549, 2548t
in cystic fibrosis, 2176
diagnosis of
algorithm for, 2551f
biopsy in, 2551. See also Liver biopsy
vs. DIC, 916
imaging in, 2550–2551, 2551t, 2556
in jaundiced patient, 318
laboratory tests in, 2550, 2550t, 2556
liver function tests in. See Liver function tests
drug-induced, 2584, 2587t, 2620t
acetaminophen in, 319, 472, 2586t, 2588,
2589f, A13
amiodarone in, 2590
amoxicillin-clavulanate in, 2589–2590
anabolic steroids in, 2590
antiretrovirals in, 2591
clinical features of, 2586t
in exacerbation of preexisting liver disease,
2553
herbal medicines in, 2590–2591
idiosyncratic, 2584, 2586t
isoniazid in, 2586t, 2589
mechanisms of, 2584–2586, 2585f
nitrofurantoin in, 2589
oral contraceptives in, 2586t
statins in, 2590
in TB, 1374
treatment of, 2586
trimethoprim-sulfamethoxazole, 2590
valproate in, 2589
in dyskeratosis congenita, 3682
effect on drug concentration response, 470
etiology of, 2547, 2547t
family history in, 2548–2549
folate deficiency in, 773
genetic considerations in, 2548–2549, 3235
grading of, 2551–2552
in GVHD, 900, 900t
in hemochromatosis. See Hemochromatosis
in hepatitis. See Hepatitis
hepatocellular, 2547, 2547t
in IBD, 2482
immunization recommendations for, 984f
in leptospirosis, 1420
liver transplantation for. See Liver
transplantation
in NAFLD. See Nonalcoholic fatty liver disease
(NAFLD)
obesity and, 3086
during parenteral nutrition, 2544
patterns of, 2547, 2547t
peripheral blood smear in, 428f, 434f
physical examination in, 318, 2549
in pregnancy, 3767
risk factors for, 2547–2549
in sarcoidosis, 2832
in schistosomiasis, 1787
in sickle cell disease, 759t
specialized nutritional support in, 2545
staging of, 2551–2552
stem cell therapy for, 3799
telomere defects in, 3683, 3684f
thyroid hormone levels in, 2945
toxic, 2584, 2586t
tumors. See Liver tumors
in type 2 diabetes mellitus, 3101
in Wilson’s disease, 2549, 3235
“Liver flap,” 2632
Liver flukes
cholangiocarcinoma and, 653
clinical features of, 1697, 1788–1789, 1789t
diagnosis of, 1788–1789, 2652, S12
epidemiology of, 1784t, S12
transmission of, 1784t
treatment of, 1788t, 1790
Liver function tests, 2553
abnormal, evaluation of, 2550, 2551f, 2553,
2554f
blood ammonia, 2555–2556
coagulation factors, 2555
global considerations in, 2556
serum albumin, 278, 357, 2537, 2538t, 2541,
2555
serum bilirubin. See Bilirubin, serum
serum enzymes, 2553. See also Alanine
aminotransferase (ALT); Alkaline
phosphatase (ALP); Aspartate
aminotransferase (AST); γ-glutamyl
transpeptidase (GGT)
serum globulins, 2555
shortcomings of, 2553
urine bilirubin, 316, 2553, 2556t, 2557
use of, 2556, 2556t
Liver pain, 2548
Liver phosphorylase deficiency (type VI GSD, Hers
disease), 3263t, 3265
Liver phosphorylase kinase deficiency (type IX
GSD), 3263t, 3264
LiverTox website, 2588
Liver transplantation, 2633
for acute intermittent porphyria, 3244
for alcohol-associated liver disease, 2618, 2619,
2641
for ATTR amyloidosis, 883
for autoimmune hepatitis, 2616
INDEX
I-130 Liver transplantation (Cont.):
for branching enzyme deficiency, 3265
candidate selection for, 2634–2635, 2636t
in children, 2634, 2634t
for cholangiocarcinoma, 655
complications of, 2638
graft rejection, 2639, A13
hepatic, 2638t, 2639
infections, 1141t, 1145, 2639
nonhepatic, 2638–2639, 2638t
recurrence of primary disease, 2635, 2640–2641
contraindications to, 2635, 2635t
for Crigler-Najjar syndrome, 2559
deceased-donor selection for, 2635–2636
for erythropoietic protoporphyria, 3248
frequency of, 2633–2634
for glucose-6-phosphatase deficiency, 3262
HAV recurrence following, 2640
HBV reinfection/recurrence following, 2602, 2640
HCV treatment before or after, 2613, 2640–2641
HDV reinfection following, 2603
for hemochromatosis, 3234
for hepatocellular carcinoma, 649t, 650
history of, 2633
immunosuppressive therapy for, 2637–2638
indications for, 2634, 2634t
living-donor, 2636
MELD score and, 2552
for metastatic NETs, 670
Milan criteria for, 650
for NALFD, 2623
orthotopic, 2633
outcome of, 2633, 2639–2641
PELD system in, 2552
quality of life after, 2641
surgical technique for, 2636–2637, 2636f
timing of, 2634
for Wilson’s disease, 3237
Liver tumors, 643
benign, 657
cholangiocarcinoma. See Cholangiocarcinoma
fibrolamellar hepatocellular carcinoma, 656
hepatoblastoma, 656
hepatocellular carcinoma. See Hepatocellular
carcinoma (HCC)
metastatic
ascites with, 323
colorectal cancer, 641
NETs, 670
Liver X receptor, 2642
Living will, 76
Lixisenatide, 3110t, 3111
LKM antibodies, 2575, 2604, 2615
LLO (listeriolysin O), 953, 1209
LMNA gene mutations, 1956t, 3649, 3650t, 3734
LMO-2 gene, 3686
LMWH. See Low-molecular-weight heparin
(LMWH)
LMX1B gene mutations, 2347
LMYC gene mutations, 500
LNK gene mutations, 803
Loading dose, 468, 468f
Loa loa (African eye worm)/loiasis
characteristics of parasite, 1778t, 1782
clinical features of, 1699t, 1782–1783, 1782f
diagnosis of, 945t, 1783, S12
epidemiology of, 945t, 1697, 1699t, 1778t, 1782
pathogenesis of, 1697, 1783
prophylaxis for, 1783
treatment of, 1708, 1783
Lobar hemorrhage, 225, 3350. See also Intracranial
hemorrhage
Lobectomy
lung, 601–603
temporal, 3321
Lobeline, 3592t
Lobular carcinoma or neoplasia in situ (LCIS), 617
Local anesthetics, 262, 3595t
Local heat urticaria, 2722
Locked-in state, 184, 3332
Lockjaw (trismus), 1212
Locus coeruleus, 3538, 3538f
Locus control region, 756, 3643
Locus (nonallelic) heterogeneity, 3649–3650, 3650t,
3663
Lod score, 3656
Loeys-Dietz syndrome, 1816, 2102, 2105,
3229–3230, 3229t
Lofexidine, 3572
Löffler’s endocarditis, 449, 1969
Löffler (Loeffler’s) syndrome, 449, 1697, 1699t,
2165, 2166t
Löfgren’s syndrome, 2830, 2831
Logopenic primary aphasia, 199
LOH (loss of heterozygosity), 501, 502f
Lomentospora infections, 1689–1690, 1689t
Lomitapide, 3142t, 3150
Lomustine (CCNU), 540t, 703
Lonafarnib, 2603
Lone Star tick, 1437, 3609
Long-chain fatty acids/triglycerides, 2459–2460, 2468t
Longevity. See Life expectancy
Longevity dividend, 3736
Long QT syndrome
arrhythmia in, 1869
clinical features of, 157, 1924
congenital, 478, 1924, A8
ECG in, 1924f, A8
etiology of, 1925t
genetic considerations in, 157, 1924–1925, 1925t
genetic testing for, 3667t
sudden cardiac death in, 2260, 2261t
treatment of, 1929, 2265t, 3667t, 3668
Long-term care, 46–47
Long terminal repeats (LTRs), 1522, 1531, 1531f
Lonomia obliqua, 3615
Loop diuretics
actions of, 342, 2291f, 2293
adverse effects of, 349, 350, 366
for CKD, 2313
for heart failure, 1943
for hypercalcemia, 357, 3184t
for hypercalcemia of malignancy, 723
for hyperkalemia, 355
for hypertension, 2084
for hypokalemia, 352
for hyponatremia, 346
for pulmonary edema, 2256
Loop of Henle
disorders involving, 2292t
embryologic development of, 2288
functions of, 2291f, 2293
in water absorption/excretion, 339, 339f
Looser’s zones, 3169
Loperamide
for diarrhea, 302, 306, 542, 555
for fecal incontinence, 2503
for IBS, 2494, 2496t
for microscopic colitis, 304
for travelers’ diarrhea, 1065t
Lopinavir, 1590f
LOPS (loss of protective sensation), 3103
Lorazepam
for acute alcohol intoxication, 3561
for anxiety disorders, 3544t
for delirium, 83t, 84
for dyspnea, 81t
for insomnia, 84, 212
for lumbar puncture analgesia, S9
for nausea and vomiting, 80, 294, 294t
overdosage/poisoning with, 3592t
pharmacology of, 3544t
for sedation after STEMI, 2060
for status epilepticus, 2224, 3322f
during terminal weaning, 86
Lorcaserin, 3092
Lordotic posture, 3518, 3520f
Lorlatinib, 513t, 544, 546t, 607
Losartan
adverse effects of, 3252
for aortic regurgitation, 1989
drug interactions of, 471t
genetic variations in response to, 476t, 478
for heart failure, 1948t
for hypertension, 2083t
metabolism of, 467t, 468, 478
for Raynaud’s phenomenon, 2785
Loss aversion, 3776–3777, 3776t
Loss function, 3829, 3829t
Loss of heterozygosity (LOH), 501, 502f
Loss of protective sensation (LOPS), 3103
Lottery-based reward systems, for health behavior,
3778, 3779, 3780, 3780f, 3782
Lotus valve, 2070
Louse-borne diseases
epidemic typhus. See Epidemic (louse-borne)
typhus
relapsing fever. See Relapsing fever
Lovastatin, 1703t, 2847t, 3142t. See also Statins
Low- and middle-income countries
financing and providing health services in,
49–50, 49t, 50t
health challenges in
brain drain, 3709
burden of disease, 3705, 3706t, 3719, 3720f
cancer, 3711–3712
cardiovascular disease, 1812–1813, 1812f,
3711
child mortality, 3719, 3721f
diabetes, 3711
Ebola virus disease, 3710
health system performance, 3721, 3721f
HIV/AIDS, 1535–1537, 1536f, 3707–3708,
3707f, 3708f
life expectancy, 3719, 3720f, 3721f
malaria, 3709–3710
skews in research, 3722
social stratification, 3722
TB, 3709–3710
primary care in, 3719
experiences with, 3703–3726, 3724f
opportunities to build, 3725–3726
revitalization of, 3722–3723
smoking patterns in, 1813
Low-density lipoprotein (LDL) apheresis, 3141,
3150
Low-density lipoprotein cholesterol (LDL-C)
atherosclerosis and, A10
composition of, 3135, 3136f
elevated levels of. See Hypercholesterolemia
(elevated LDL-C)
estimate of, 3137
low levels of, 3139t, 3140t, 3145–3146. See also
Abetalipoproteinemia
oxidized, 2696t
in transport of hepatic lipids, 3136, 3137f
INDEX
Lower esophageal sphincter (LES), 288, 2427, 2428f I-131
Lower motor neuron diseases, 734, 3413t, 3415. See
also Amyotrophic lateral sclerosis (ALS)
Lower motor neuron pathways, 166f
Lower motor neuron (neuropathic) weakness, 165,
165t, 168
Lower urinary tract symptoms (LUTS), 3075
in benign prostatic hyperplasia, 688, 689t, 2374.
See also Benign prostatic hyperplasia
(BPH)
hematuria in, 2283–2284
in IC/BPS, 325, 328
Low-fat diet, 490
Low FODMAP diet, 296
Low-molecular-weight heparin (LMWH), 931
actions of, 929f, 931
adverse effects of, 932
for antiphospholipid antibody syndrome, 2751
assessment of, 456
discontinuation before lumbar puncture, S9
dosage of, 932
for DVT/PE treatment, 2098, 2099t, 3766
vs. fondaparinux, 932t
vs. heparin, 931t
monitoring treatment with, 931–932
pharmacology of, 931
for STEMI, 2050t, 2051, 2061
thrombocytopenia induced by. See Heparininduced thrombocytopenia
for thrombophlebitis, 727
for VTE prophylaxis, 2100t, 3773
Loxapine, 3555t
LOX gene mutations, 3229t
LP(a). See Lipoprotein(a)
LPL. See Lipoprotein lipase (LPL)
LPL (lipoprotein lipase) deficiency, 3138, 3688
LPS. See Lipopolysaccharide (LPS)
LPS-binding protein, 2674
LPS receptor. See CD14 (LPS-receptor)
Lp-X, 3144
LRBA gene mutations, 2704t
LRP4 antibodies, 3510
LRP5 gene mutations, 3193
LRRK2 gene mutations, 2472t, 3297, 3389, 3391t,
3392
LSC1 gene mutations, 2118
LSD, 3576
LT4. See Levothyroxine (LT4)
LTA4H gene, 968
LTRs (long terminal repeats), 1522, 1531,
1531f
LT-β, 2682t
Lubiprostone, 79, 307, 308, 2495, 2496t
Lubricin, 2755–2756, 2855
Lucey-Driscoll syndrome, 2558
Lucio’s phenomenon, 1037, 1387
177Lu-dotatate, 553, 669f, 671, 671t, 720
Ludwig’s angina, 256, 1351
Lues maligna, 1408, 1571
Lujo virus, 1626t
Lumacaftor, 477t, 2178
Lumateperone, 3555t
Lumbar adhesive arachnoiditis, 123
Lumbar fractures. See Vertebral fractures
Lumbar lordosis, 321
Lumbar puncture, S9
analgesia for, S9
in coma, 187
headache following, 116, S9
imaging and laboratory studies prior to, S9
in meningitis, 1103
in neurologic critical illness, 2269
in patient receiving anticoagulants or antiplatelet
agents, S9
positioning for, S9
in subarachnoid hemorrhage, 3355
technique, S9
Lumbar spinal lesions, 3446
Lumbar spinal stenosis, 121, 122f
Lumbar spine
congenital anomalies of, 124
disk disease in, 118f, 120–121, 121f
disk replacement in, 126
fusion surgery in, 126
pain referred to, 124
Lumbosacral plexopathies, 3500, 3500t
Lumbosacral plexus, 3499–3500, 3500f
Lumbo virus, 1627t
Lumefantrine, 1702t, 1709, 1732t
Luminal A breast cancer, 617, 620
Luminal B breast cancer, 618, 620
Luminal bile salt deficiency, 2461, 2461f, 2461t
Luminal digestion, 2458, 2460. See also
Malabsorption
Lumpectomy, 617, 618
Lung
airways resistance in, 2139
blood flow through, 2133
compliance of, 2134, 2222
diffusing capacity of, 2139
elastic recoil pressure of, 2134
flow-related properties of, 2134–2135, 2135f,
2139
shunt, 2136, 2137f
volume-related properties of, 2133–2134, 2134f,
2135f, 2138–2139
Lung abscess, 1020
anaerobic bacterial, 1352, 1353f
approach to the patient, 1022
clinical features of, 1021
complications of, 1022, 1118
definition of, 1020
diagnosis of, 1021
differential diagnosis of, 1021
epidemiology of, 1020
etiology of, 1020, 1020t, 1352
hemoptysis in, 270
pathogenesis of, 1020–1021, 1021f
pathology and microbiology of, 1020t, 1021
in pneumonia, 1015
prevention of, 1022
prognosis of, 1022
treatment of, 1021–1022
Lung allocation score (LAS), 2209, 2211
Lung biopsy
in granulomatosis with polyangiitis, A14
in hypersensitivity pneumonitis, 2161–2162,
2162f
in interstitial lung disease, 2192, 2194f
in microscopic polyangiitis, A14
in pulmonary infection, 561
in vasculitic syndromes, A14
Lung cancer, 594
adenocarcinoma, 595, 595f
airway obstruction in, 572
asbestos-related, 2168
carcinoma of unknown primary and, 717, 718t
classification of, 595, 595f
clinical features of, 498–599, 598t
clubbing in, 275
COVID-19 disease and, 611
deaths from, 481t, 482f, 484t
diagnosis of, 599, A12
epidemiology of, 594
genetic considerations in, 500t, 595–597, 596f,
597t
hemoptysis in, 271, 571
immunohistochemistry of, 596
incidence of, 481t, 482, 482f, 484t
large cell, 595, 595f
lymphadenopathy in, 458
metastatic
to bone, 715
clinical features of, 598–599, 598t, 2875
to CNS, 708f, 708t
to eye, 227
to heart, 2027, A9
incidence of, 598
to skin, 398
treatment of
cytotoxic chemotherapy, 608–609, 608t
immunotherapy, 607–608, 608f, 608t
molecular targeted therapy, 511, 606–607,
606t, 607f, 607t
second-line therapy, 609
supportive care, 609
non-small-cell
genotyping for, 3838
metastatic, 708f
pathology of, 595, 595f
prognosis of, 602f
staging of, 599–601, 600f, 601t
treatment of
ablative therapies for early-stage, 2216
chemotherapy in stages I and II, 604–605,
605t
for occult and stage 0 carcinomas, 602
for Pancoast tumors, 606
radiation therapy in stages I and II, 603–604
for solitary pulmonary nodule and “groundglass” opacities, 602, 603t, 604f
in stage III, 605–606
in stage IV. See Lung cancer, metastatic
surgical resection in stages I and II,
602–603
survival, 602f
treatment of, 602, 603f
tumor markers in, 487t
occupational exposures and, 2171–2172
paraneoplastic syndromes in, 598–599, 722t,
725t
pathogenesis of, 596–597
pathology of, 595–596, 595f
prevention of, 492
racial/ethnic disparities in treatment of,
60
radon exposure and, 2172
risk factors for, 594–595
screening for, 496t, 497, 597–598, 598t, 3745t
second malignancies in survivors of, 740
small-cell
hypokalemia in, S1
immunohistochemistry of, 596, 2696t
intestinal pseudoobstruction in, 292
Lambert-Eaton myasthenic syndrome in, 599,
729, 3513
paraneoplastic syndromes in, 722, 722t, 729,
729t, 3508
pathology of, 595, 595f
SIADH in, 343, S1
staging of, 601
treatment of, 609f
chemotherapy, 609–610
prophylactic cranial irradiation, 610
surgery, 609
thoracic radiation therapy, 610
INDEX
I-132 Lung cancer (Cont.):
smoking and, 490, 595, 3563t
squamous cell, 595, 595f
staging of, 599–602, 600f, 601t
stem cells in, 596
superior vena cava syndrome in, 565, 566f, 598,
598t
in women, 3068
Lung disease. See also Respiratory disorders; specific
disorders
air pollution and, 2172
barotrauma-related, 3629
biomass smoke-induced, 2172–2173, 2173f
cancer. See Lung cancer
cyanosis in, 274
in cystic fibrosis, 2176. See also Cystic fibrosis
(CF)
deaths from, 73t
global considerations in, 2172–2173
high-altitude travel and, 3622
IgG4-related, 2838t
indoor exposures and, 2172–2173
infections in cancer patient, 560–561, 561t
in leptospirosis, 1419f
occupational. See Occupational illness, lung
disease
in osteogenesis imperfecta, 3223
parasitic infections, 1699t
pulmonary hypertension in, 2126
respiratory acidosis in, 366
in rheumatoid arthritis, 2753
in sarcoidosis, 2830–2831, 2832f
in SLE, 2742–2743, 2743t
in systemic sclerosis, 2776–2777, 2777f,
2780–2781, 2780f
Lung flukes (Paragonimus spp.)
clinical features of, 1699t, 1789t, 1790
diagnosis of, S12
eosinophilia caused by, 945t
epidemiology of, 270, 945t, 1697, 1699t, 1784t,
1789, S12
hemoptysis caused by, 270
life-cycle hosts of, S12
treatment of, 1713, 1790
Lung injury, acute, 2226, 2227f, 2228. See also
Acute respiratory distress syndrome
(ARDS)
Lung lavage, S5
Lung transplantation
contraindications to, 2210–2211, 2210t
for COPD, 2188
for cystic fibrosis, 2179, 2210
donor considerations, 2211–2212, 2212t
donor management, 2212
donor operation, 2212
for idiopathic pulmonary fibrosis, 2193, 2210
immunosuppression for, 2213
indications for, 2209–2210
infections in recipient, 1141t, 1144
outcomes of, 2214t
perioperative considerations and complications,
2213
recipient management, 2211, 2213–2214
recipient operation, 2212–2213
in systemic sclerosis, 2786
Lung volume(s), 2133–2134, 2135f, 2138–2139,
2182–2183
Lung volume reduction surgery, 2188
Lungworm, rat. See Angiostrongylus spp. infections
Lupus anticoagulants
in antiphospholipid syndrome, 2749
laboratory evaluation of, 456, 2745, 2749t
in SLE, 2745
in thrombotic disease, 919
warfarin therapy and, 935
Lupus dermatitis, 2746, 2748
Lupus erythematosus
acute cutaneous, 405, 405f
clinical features of, 397
discoid. See Discoid (chronic cutaneous) lupus
erythematosus
drug-induced, 378, 409, 472, 478, 2748–2749,
2847t
subacute cutaneous, 396, 406, 2740, A1
systemic. See Systemic lupus erythematosus
(SLE)
Lupus hairs, 384
Lupus nephritis
classification of, 2338, 2338t, 2739, 2739t
clinical features of, 2335t, 2338, 2359, 2740–
2741, 2743t
membranous, 2747
pathogenesis of, 2332, 2337–2338
prognosis of, 2338
renal biopsy in, 2338, A4
treatment of, 2338, 2741, 2744t, 2746–2747
Lupus panniculitis, 397
Lupus pernio, 397, 2831, 2832f
Lupus profundus, 2740
Lupus vulgaris, 397
Lurasidone, 3551, 3555t
Lurbinectedin, 539, 540t, 609–610
Lusitropic effect, 1806f
Luspatercept, 763, 802, 862
Lutein, 2530
Luteinizing hormone (LH), 2895
actions of, 2886, 2895, 3029–3030
androgen deficiency and, 3020
deficiency of, 2899t
ectopic production of, 722t
expression and regulation of, 2892t, 2893f
feedback control of, 2891
in females, age-related changes in levels of,
3028–3029, 3029f
GnRH and, 2891
laboratory evaluation of, 2898t, 3010
in male pubertal development, 2906
in menstrual cycle regulation, 3031, 3031f
in ovarian follicle development, 3027–3028,
3027f
ovulation and, 3031
in perimenopause, 3043, 3043f
secretion of, 207, 2895, 3028
synthesis of, 2895
Luteinizing hormone (LH) receptor, 2882, 2887,
2888t, 3002, 3651
Luteinizing hormone-releasing hormone (LHRH)
agonists, 515, 543–544, 613t
Luteinizing hormone (LH) therapy, 3021
LUTS. See Lower urinary tract symptoms (LUTS)
LVR (laparoscopic ventral rectopexy), 2502, 2502f
Lycopene, 2530
Lyme borreliosis (Lyme disease), 1425
chronic, 1428, 1430
climate change and, 1006, 1006f
clinical features of, 135t, 385, 1427
arthritis, 1043, 2696t
AV conduction block, 1427, 1882, A8
chronic meningitis, 1113t
disseminated infection, 1427
erythema migrans, 135t, 141, 385, 1427, 1427f,
A1
evolution of, 135t, 141, 385, 1427
facial palsy, 3440
localized infection, 1427
myocarditis, 1962
neuropathy, 3412, 3490
persistent infection, 1427–1428
co-infection with Babesia, 1430, 1736, 1739
diagnosis of, 961, 973, 1428–1429, 1428t, A16
differential diagnosis of, 141, 1429
epidemiology of, 1426
etiology of, 1425–1426
global considerations in, 1426
pathogenesis of, 1426–1427
prevention of, 1430, 3609
prognosis for, 1430
prophylaxis for, 1430, 3609–3610
regional variations in, 1428
reinfection in, 1430
ticks in, 1426, 3609
treatment of, 1043, 1428t, 1429–1430, 1430f
Lymphadenitis, tuberculous, 1364, 1364f
Lymphadenopathy, 457
approach to the patient, 457–458
benign, 458
diseases associated with, 458t
in fever of unknown origin, 151
in Hodgkin’s lymphoma, 853
IgG4-related, 2838t, 2840
infections associated with, 458, 458t, 943–944
Brucella, 1312
cat-scratch disease, 1329, 1330f
HIV infection, 1543–1544, 1574. See also HIV
infection
human African trypanosomiasis, 1754
nontuberculous mycobacteria, 1394
plague, 1322, 1322f
tularemia, 1317
laboratory evaluation of, 459
localized/regional, 458
in secondary syphilis, 384
in Sjögren’s syndrome, 2789t
with splenomegaly, 458–459
thoracic/abdominal, 459
Lymphangiectasia, intestinal. See Intestinal
lymphangiectasia
Lymphangiography, 2120
Lymphangioleiomyomatosis, pulmonary, 2190,
2191, A12
Lymphangitis, 1193, 2119, 2120
Lymphatic filariasis, 1778
clinical features of, 1045, 1779–1780, 1779f,
2119, S6
diagnosis of, 1780, S6, S12
differential diagnosis of, 1780
epidemiology of, 1697, 1778–1779, 1778t
incubation period for, S6
pathogenesis of, 1697, 1779
prevention and control of, 1780
treatment of, 1045, 1708, 1780, S6
Lymphatic obstruction, 278, 304
Lymphedema, 2118
anatomic considerations in, 2118
clinical features of, 2119, 2119f
congenital, 2118–2119
diagnosis of, 2120
differential diagnosis of, 2119–2120
etiology of, 2118–2119, 2119t
in lymphatic filariasis, 1779–1780, 1779f,
2119
pathophysiology of, 278, 2118
stages of, 2119, 2120t
treatment of, 1780, 2120
Lymphedema praecox (Meige’s disease/syndrome),
2118, 2199, 3402
INDEX
Lymphedema tarda, 2118 I-133
Lymph node biopsy, 458, 459
Lymphocyte(s)
B. See B cell(s)
endothelial cell interactions of, 2698–2699,
2698f, 2699t
large granular, 425, 444. See also Natural killer
(NK) cells
in nutrition assessment, 2538t
in peripheral blood smear, 425, 430f
reactive, 425
T. See T cell(s)
tumor-infiltrating, 2702
Lymphocytic choriomeningitis (LCM), 1106, 1108,
1114t, 1626t, 1639
Lymphocytic colitis, 2480
Lymphocytic gastritis, 2457
Lymphocytic hypophysitis, 2897
Lymphocytic meningitis, 1115t
Lymphocytic variant hypereosinophilia, 862, 863t
Lymphocytoma cutis, 396, 397
Lymphogranuloma venereum (LGV)
clinical features of, 1090f, 1091t, 1448, 2119
complications of, 1448
diagnosis of, 1449t
epidemiology of, 1079–1080, 1089–1090, 1448
lymphadenopathy in, 458
Lymphohistiocytosis, hemophagocytic, 141,
2717–2718, S8
Lymphoid hyperplasia, cutaneous
(pseudolymphoma), 384, 396
Lymphoid malignancies, 855. See also Hodgkin’s
lymphoma; Leukemia; Non-Hodgkin’s
lymphoma; Plasma cell disorders
anemia in, 432
approach to the patient, 844–846
B cell
B-cell prolymphocytic lymphoma, 855–856
hairy cell leukemia. See Hairy cell leukemia
immunophenotypes of, 856t
intravascular large B-cell lymphoma, 857
lymphomatoid granulomatosis, 857
mediastinal (thymic) large B-cell lymphoma,
857
nodal marginal zone B-cell lymphoma,
848–849, 856–857
primary effusion lymphoma, 857
B-cell development and, 842–843, 843f
carcinoma of unknown primary and, 718t
classification of, 840t, 855t
CNS, primary. See Primary central nervous
system lymphoma (PCNSL)
deaths from, 481t, 484t
diagnosis of, 844–845
differential diagnosis of, 1486t
EBV infection and, 1485
erythrophagocytosis in, A6
etiology of, 842t, 1485
extranodal NK/T-cell lymphoma, nasal type,
841, 851, 858, 2807
fever in, 132, 147, 151
genetic considerations in, 842–844, 844t
in HIV infection, 1583–1584, 1583f, 1584f
incidence of, 481t
infections in, 560
lymphadenopathy in, 458
neuropathy in, 3492
nodular follicular, A6
non-Hodgkin’s subtypes. See Non-Hodgkin’s
lymphoma, subtypes
ocular invasion by, 227
oral manifestations of, 259t, 1583f
paraneoplastic syndromes in, 721, 722t
pleural effusion in, 489
proteinuria in, 336
in rheumatoid arthritis, 2753
in Sjögren’s syndrome, 2788t, 2789
skin manifestations of, A5
small intestinal, 635–636
splenomegaly in, 461
T cell
extranodal T/NK-cell lymphoma, nasal type,
2807
hepatosplenic T-cell lymphoma, 2485
large granular lymphocytic leukemia, 2753
T cell and NK cell
aggressive NK-cell leukemia, 858
angioimmunoblastic T-cell lymphoma, 844t,
850, 858–859
blastic NK-cell lymphoma, 858
enteropathy-type T-cell lymphoma, 851, 858
extranodal NK/T cell, nasal type. See
Extranodal NK/T-cell lymphoma, nasal
type
hepatosplenic T-cell lymphoma, 844t, 851, 858
primary cutaneous CD30+ T-cell lymphoma,
858
subcutaneous panniculitis-like T-cell
lymphoma, 851, 858
T-cell large granular lymphocytic leukemia,
857–858
T-cell prolymphocytic leukemia, 436, 857
T cell development and, 843–844, 844f
in thymus. See Thymoma
in thyroid, 2952–2953
in transplant recipient, 2275
tumor markers in, 487t
urticaria in, 143
Lymphoid tissue, mucosa-associated. See Mucosaassociated lymphoid tissue (MALT)
Lymphoma. See Lymphoid malignancies
Lymphoma cutis, 396, 397
Lymphomatoid granulomatosis, 857, 2807
Lympho-occlusive bandage, for snakebite,
3598
Lymphoplasmacytic lymphoma, 841, 844t, 849
Lymphoplasmacytic sclerosing pancreatitis. See
IgG4-related disease (IgG4-RD)
Lymphoscintigraphy, 2120
Lymphotactin/SCM-1, 2683t
Lynch syndrome (hereditary nonpolyposis colon
cancer)
associated lesions in, 638, 638t
bladder cancer and, 677
characteristics of, 638
clinical features of, 638
early interventions for, 3667t, 3668
endometrial cancer in, 699
epigenetic silencing in, 516
genetic considerations in, 503t, 638
APC tumor-suppressor gene, 499f,
503
DNA mismatch/repair, 3642, 3648
MLH1 gene mutations, 503, 503t, 516, 638,
658t, 3648
MSH2 gene mutations, 638
somatic mutational steps, 499f
genetic testing for, 3667t
ovarian cancer in, 695
polyp distribution and characteristics in,
638t
screening for, 638, 3648
small-bowel adenocarcinoma in, 635
type II, 695
Lyonization, 914
Lysine metabolism disorders, 3270t
Lysine methylation, 3792
Lysinuric protein intolerance, 3274, 3275t
Lysinuric protein intolerance (dibasic
aminoaciduria), 2292t
Lysosomal acid lipase deficiency (cholesteryl ester
storage disease), 3139t, 3142–3143,
3257t, 3260
Lysosomal storage diseases, 3254
genetic considerations in, 3254, 3258
glycogen disorders, 3257t. See also Pompe
disease (acid α-1,4 glucosidase
deficiency)
glycoproteinoses, 3256t
GM2
gangliosidoses, 3255–3256t. See also TaySachs disease
leukodystrophies, 3256t
mucolipidoses, 3256t
mucopolysaccharidoses, 3255t, 3259–3260, A15
neutral glycosphingolipidoses
Fabry disease. See Fabry disease
Gaucher disease. See Gaucher disease
Niemann-Pick diseases, 3256t, 3259
neutral lipid disorders, 3257t
pathogenesis of, 3254–3255, 3258
treatment of, 3258
Lysosome(s), 954–955, 3254
Lysozyme, 954–955
Lyssaviruses, 1618, 1623. See also Rabies
LYST protein, 447
M
Machado-Joseph disease (SCA3), 3424–3425, 3655t
Machine learning, 3826
applications to clinical medicine, 3829–3830
medical, 3827–3828, 3827t, 3828f
practical concepts for, 3829, 3829t
precision medicine and, 3830, 3830f
types of, 3826–3827, 3826f, 3827t
Machine operator’s lung, 2160t
Machupo/Bolivian hemorrhagic fever, 1626t,
1642
Maciel virus, 1628t
MAC infections. See Mycobacterium avium
complex (MAC) infections
Macitentan, 2127–2128, 2129t
MACOP-B regimen, 857
Macroalbuminuria, 2076
Macroamylasemia, 2669
Macrocytosis, 426f, 432, 434f
Macroglossia, 261t, 880, 880f
Macrolides. See also specific drugs
actions of, 1149, 1159, 1164t
adverse effects of, 414, 1154t, 1159,
1705t
for community-acquired pneumonia, 1014,
1014t
drug interactions of, 1155t, 1705t
indications for, 1159
for Legionella spp. infections, 1256t
for pertussis, 1260, 1261t
resistance to
manifestations of, 1013
mechanisms of, 1164t, 1166–1167
in M. pneumoniae, 1013, 1443
in pneumococci, 1013, 1175–1176
prevalence of, 1191
in T. pallidum, 1412
Macronutrient malnutrition, 2540. See also
Malnutrition
Macroovalocytes, 426f, 434f
INDEX
I-134 Macrophage(s)
in adaptive immunity, 2679t, 2680f
in autoimmunity, 2733
brain, 3293–3295
development of, 2680f
functions of, 447–448
in HIV infection, 1549–1550
in innate immunity, 2676, 2679t
in pneumonia, 1010
in smokers, 2182
in TB, 1361
Macrophage colony-stimulating (M-CSF),
2682t
Macrophage-defined chemokine (MDC), 2683t
Macrophage inflammatory proteins, 443, 1554,
2683t
Macroreentrant atrial tachycardia, 1899, 1901f,
1902f
Macrothrombocytopenia, 904f
Macula, 215, 218
Macula densa, 2288, 2289f
Maculae ceruleae, 3611
Macular amyloidosis, 395
Macular degeneration, 226, 226f
complementary and integrative therapies for,
3786
gene therapy for, 3688
prevention of, 2530
stem cell therapy for, 3304
Macular hole, 227
Maculatum disease, 1432t
Macules, 133, 260t, 369t, 370f
Maculopapular cutaneous mastocytosis, 2730
Madrid virus, 1627t
Madurella, 1688
Mafenide acetate, S4
Maffucci’s syndrome, 397, 3216
MAG (myelin-associated glycoprotein), 876, 2696t
Maggots, 3611
MAGIC syndrome, 2828
Magnesium, 2520t, 3164
deficiency of. See Hypomagnesemia
excess of. See Hypermagnesemia
renal transport of, 2291f, 2293
Magnesium citrate, 80t
Magnesium hydroxide, 80t, 2443, 2495, 2496t
Magnesium sulfate, 1213, 3763
Magnesium supplements, 237, 3201
Magnesium-wasting syndromes, 3164, 3165t
Magnetic resonance angiography (MRA)
in frostbite, 3635
in neurologic disease, 3288–3290
in peripheral artery disease, 2108, 2108f
phase-contrast, 3288
of renal arteries, 2089, 2089t
of thoracic aneurysm, 2103f
time-of-flight, 3285f, 3288, A16
vessel wall, 3288–3290, 3288f
Magnetic resonance cholangiopancreatography
(MRCP)
in bile duct disease, 2410, 2415f, 2651t
in cholestatic disease, 319
in liver disease, 2550
in pancreatic disease evaluation, 2653, 2653f,
2654t, 2655, 2656
in primary sclerosing cholangitis, 2628
Magnetic resonance elastography, 2550–2551,
2551t, 2556
Magnetic resonance imaging (MRI)
in adrenocortical carcinoma, 2969f
in axial spondyloarthritis, 2792f, 2794
for body composition study, 2537, 2538t
for breast cancer screening, 495t, 496, 615–616
in CAH, 2975f
in cardiac disease. See Cardiac magnetic
resonance imaging (CMR)
in coma, 187
contraindications to, 3287–3288, 3288t
in Crohn’s disease, 2477, 2478f
in Cushing’s syndrome, 2963, 2964f
FLAIR. See Fluid-attenuated inversion recovery
(FLAIR) MRI
in hearing loss evaluation, 245
in liver disease, 2550, 2551t
in lymphadenopathy, 459
in lymphedema, 2120
in mastoiditis, 251
in Ménière’s disease, 241
in musculoskeletal disease evaluation, 2853,
2853t, 2854f
in neurologic disease. See also Neuroimaging,
MRI
acute disseminated encephalomyelitis, A16
acute transverse myelitis, A16
adrenoleukodystrophy, A16
amyotrophic lateral sclerosis, 3411f
arteriovenous malformation, A16
Bell’s palsy, 3440, 3441f, A16
brachial plexopathy, A16
brain abscess, 1118, 1119f
brain metastases, 708, 708f
brain tumors, 701–702, 703f, 704f, 3290f, A16
CADASIL, A16
Candida infection, in brain, A16
cavernous malformation, 3288f
cerebral abscess, 3286f
cerebral arteriopathy, 3289f
cerebral small-vessel disease, 3383–3384f
cobalamin deficiency myelopathy, A16
coccidiomycosis meningitis, A16
cranial epidural abscess, 1123
Creutzfeldt-Jakob disease, 421f, 3422
dementia, 193, 193f
DLB, 3385t
encephalitis, 1095–1096, 1096f, 1096t, 3287f
epidural metastases, 710f
FTD, 3379f
Guillain-Barré syndrome, A16
Hashimoto’s encephalopathy, A16
hemiplegic migraine, A16
hepatic encephalopathy, A16
histiocytosis, A16
Huntington’s disease, 3405f, A16
hyperperfusion disorder, 2274–2275, 2274f
hypoxic-ischemic encephalopathy, 2272f
intracerebral hemorrhage, 3351
intramedullary astrocytoma, 3449f
Krabbe disease, A16
lacunar infarction, A16
Leigh’s syndrome, A16
leptomeningeal metastases, 709f
limbic encephalitis, A16
Lyme disease, A16
melanosis, A16
meningioma, 706f
meningitis, 1103, 1112, 1116f
mesial temporal lobe epilepsy, 3309f
metachromatic leukodystrophy, A16
migraine after radiation therapy, A16
moyamoya disease, A16
MS, 3465–3466, 3467f, A16
MS variants, 3475f, A16
multiple system atrophy, 3432, 3433f, A16
myopathy, 3520–3521
neurofibromatosis type 1, A16
neurofibromatosis type 2, A16
neuromyelitis optica, 3477, 3478f, A16
neurosarcoidosis, A16
neurosyphilis, A16
osmotic demyelination syndrome, 2273, 2273f
pilocytic astrocytoma, A16
primary central nervous system lymphoma,
705, 705f
progressive multifocal leukoencephalopathy,
1099
seizures, 3314
sickle cell disease, A16
spinal arteriovenous malformation, 3453
spinal cord infarction, 3450, A16
spinal epidural abscess, 3448–3449, 3449f
stroke, 3334, 3335f
Sturge-Weber syndrome, A16
subdural empyema, 1122f
subdural hematoma, 184f, A16
superior sagittal sinus thrombosis, A16
syringomyelia, 3453f
thoracic meningioma, 3448f
traumatic brain injury, 3459
tuberculosis, A16
tuberous sclerosis, A16
vasculitis, A16
vertebral fracture/dislocation, A16
vestibular schwannoma, 707, 707f
von Hippel–Lindau disease/syndrome, A16
in osteomyelitis, 1047, 1048f
in pancreatic disease, 2653, 2653f, 2654t, 2655
in pheochromocytoma, 2977, 2977t, 2978f
of pituitary tumors, 2903–2904, 2904f, 2906f,
2921, A16
in polydipsia, 2921
in polymyositis, 2821f
in prostate cancer staging, 683
with proton density fat fraction, 2622
in renal cell carcinoma, 674
in respiratory disease evaluation, 2145, 2145f
in rheumatoid arthritis, 2760
in sarcoidosis, 2834
of sellar masses, 2903–2904
in sinonasal aspergillosis, A16
in spinal cord compression, 569, A16
in spinal disorders, 121f, 122f
in viral encephalitis, 1096f, 3287f
in Wernicke’s disease, 2274f
Magnetic resonance neurography, 3291
Magnetic resonance spectroscopy, 3834
Magnetoencephalography (MEG), 3314
Maguari virus, 1627t
Mahaim fibers, 1897
Ma huang (Ephedra sinica), 3311t, 3787
Maintenance dose, 470
Majocchi’s granuloma, 386
Major depression, 3547–3548, 3547t, 3549f, 3823.
See also Depression/depressive disorders
Major histocompatibility complex (MHC). See
Human leukocyte antigen (HLA)
complex
MAL (methyl aminolevulinate), 418
Malabsorption disorders, 2458
approach to the patient, 2467
classification of, 2459t
clinical features of, 2467, 2468t, 3426
diagnosis of, 2465f, 2467–2469, 2468t, 2469t
in luminal phase of digestion
bile acid diarrhea, 2461, 2461t
with disordered intestinal motility, 2460
fatty acid diarrhea, 2461t
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