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GY59 Gynaecology Toronto Notes 2023
References
Agency lor Healthcare Research and Quality.Clinical Guidelines andRecommendations [Internet].Rockville (MD): U.S.Department olHealth and HumanServices:2020Sep [updated 2018 Jut:cited 2020 Jun 22].
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Hematology
Reid Gallant, Syed Shahan Haider, and Nathan Kuehnc, chapter editors
Karolina Gaebe and Alyssa Li, associate editors
Wei Hang Dai and Camilla Giovino, EB\1 editors
Dr. Matthew Cheung, Dr. Lisa Chodirker, Dr. Helena Dhamko, Dr. Zachary Liedcrman, Dr. Michael
Scott, and Dr. Martina Trinkaus, staff editors
Hematology
Acronyms
Basics of Hematology.
CompleteBlood Count
Blood Film Interpretation
Bone Marrow Aspiration and Biopsy
Common Presenting Problems
Anemia
Erythrocytosis
Thrombocytopenia
Thrombocytosis
Pancytopenia
Neutrophilia
Neutropenia
Lymphocytosis
Lymphopenia
Eosinophilia
Agranulocytosis
Leukemoid Reaction
Approach to Lymphadenopathy.
Approach to Splenomegaly
Microcytic Anemia
Iron Metabolism
Iron Deficiency Anemia
Anemia of Chronic Disease
Sideroblastic Anemia
Lead Poisoning
Normocytic Anemia
Aplastic Anemia
Hemolytic Anemia
Thalassemia
p-Thalassemia Minor (Thalassemia Trait)
P-Thalassemia Major
P-Thalassemia Intermedia
a-Thalassemia
Sickle Cell Disease
Autoimmune Hemolytic Anemia
Microangiopathic Hemolytic Anemia/Thrombotic
Microangiopathy
Hereditary Spherocytosis
Hereditary Elliptocytosis
Glucose-6-Phosphate Dehydrogenase Deficiency
Macrocytic Anemia
Vitamin B12 Deficiency
Folate Deficiency
Hemostasis.
Stages of Hemostasis
Disorders of Primary Hemostasis
Immune Thrombocytopenia
Thrombotic Thrombocytopenic Purpura and Hemolytic Uremic
Syndrome
von Willebrand Disease
Disorders of Secondary Hemostasis
Hemophilia A (Factor VIII Deficiency)
Hemophilia B (Factor IX Deficiency)
Factor XI Deficiency
Liver Disease
Vitamin K Deficiency
Disseminated Intravascular Coagulation
HI Hypercoagulable Disorders
Venous Thromboembolism
Approach to Treatment of Venous Thromboembolism
Hematologic Malignancies and Related Disorders.
Myeloid Malignancies
Acute Myeloid Leukemia
Myelodysplastic Syndromes
Myeloproliferative Neoplasms
Chronic Myeloid Leukemia
Polycythemia Vera
Idiopathic Myelofibrosis
Essential Thrombocythemia
Lymphoid Malignancies
Acute Lymphoblastic Leukemia
Lymphomas
Hodgkin Lymphoma
Non-Hodgkin Lymphoma
Malignant Clonal Proliferations of Mature B-Cells.
Chronic Lymphocytic Leukemia
Multiple Myeloma
Monoclonal Gammopathyof Unknown Significance
Lymphoplasmacytic Lymphoma
Complications of Hematologic Malignancies
Hyperviscosity Syndrome
Tumour Lysis Syndrome
Blood Products and Transfusions
Blood Products
Red Blood Cells
Platelets
Coagulation Factors
Acute Blood Transfusion Reactions
Delayed Blood Transfusion Reactions
Common Medications
Antiplatelet Therapy
Anticoagulant Therapy
Chemotherapeutic and Biologic Agents Used in Oncology
Landmark Hematology Trials
References
H35
H2 ,H36
H2
,H39
,H39
H6
H42
H46
H47
H50 H12
H13
H14
H53
H54
H17
H18
H58
H61
H63
H25
H26
H28
r i
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HI Hematology Toronto Notes 2023
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H2 Hematology Toronto Notes 2023
Acronyms
antibody
atrial fibrillation
DVT deep vein thrombosis
Epstcin- Barr virus
ethylenediamlnetetraacetic add IIP
erythropoietin
erythropoiesis-stimulating agent
erythrocyte sedimentation rate
essential thrombocythemia
fibrin degradation products
fine needle aspiration
frozen plasma
granulocyte-colony stimulating
factor
reduced glutathione
genitourinary
graft versus host disease
hemolytic anemia
hemoglobin
hepatitis B virus
hematocrit
hepatitis C virus
hemolysis,elevated liver enzymes, OCP
and low platelet count
heparin- induced thrombocytopenia PE
Hodgkin lymphoma
high molecular weight kininogen Ph
hemolytic uremic syndrome
inflammatory bowel disease
idiopathic myelofibrosis
immunomodulatory drugs
internationalnormalized ratio
intermittent pneumatic compression Pf
IPSS international prognostic scoring
system
immune thrombocytopenia
Janus kinase 2
PIT partial thromboplastin time
PUD peptic ulcer disease
PV polycythemia vera
RCMD refractory cytopenia with
multilineage dysplasia
RCMD RS refractory cytopenia with
multilineage dysplasia and ringed
Ab
AFrb EBV
AFLP acute fatty liver of pregnancy
atypical hemolytic uremic syndrome EPO
autoimmune hemolytic anemia ESA
acute lymphoblastic leukemia ESR
acute myeloid leukemia
absolute neutrophil count
activated protein C
acute promyelocytic leukemia FP
antiphospholipid antibodies
antiphospholipid antibody
EDTA
aHUS JAK:
LAD lymphadenopathy
LMWH low molecular weight heparin
MAHA/ microangiopathic hemolytic
TMA anemia/thrombotic microangiopathy sideroblasts
MCH mean corpuscular Hb
MCHC mean corpuscular Hb concentration SCD
MCV mean cotpuscularvolume
MDS myelodysplastic syndromes
myelofibrosis
MGUS monoclonal gammopathy of
unknown significance
multiple myeloma
MPN myeloproliferative neoplasm
MPV mean platelet volume
MUGA multi-gated acquisition
non-Hodgkin lymphoma
oral contraceptive pill
PCC prothrombin complex concentrates TIP
pulmonary embolism
progression-free survival
Philadelphia chromosome
proteasome inhibitors
prekalliktein
PMN polymorphonuclear neutrophil
paroxysmal nocturnal
AIHA
All
AML El
ANC FDP
APC FNA lit
'
,', RBC distribution width
sickle celldisease
stem cell transplantation
serum protein electrophoresis
soluble transferrin receptor
T-cell lymphoma
total iron binding capacity
tyrosine kinase inhibitor
T -cell large granular lymphocyte
tumour lysis syndrome
tissue plasminogen activator
thrombopoietin
thrombin time
thrombotic thrombocytopenic
API
APIA G-CSF SCT
APS SPEP
syndrome GSH MF sTfR
aPTT activated partial thromboplastin GU TCI
time GVHD TIBC
ARDS acute respiratory distress syndrome HA
ATIII antithrombin III
ATRA all-trans retinoic acid
bone marrow
CALR calreticulin
chimeric antigen receptor
Cll chronic lymphocytic leukemia
CMl chronic myeloid leukemia
CMV cytomegalovirus
CRP C-reactive protein
DAT direct antiglobulin test
ODAVP - desmopressin
DIC disseminated intravascular
coagulation
DLBCl diffuse large 8-cell lymphoma
DOAC direct oral anticoagulant
MV TKI
Hb T-lGl
HBV as
BM Hct tPA
HCV NHL TPO
CAR HELLP TT
HIT purpura
HL UFH unfractionated heparin
urine protein electrophoresis
venous thromboembolism
von Willebrand disease
von Willebrand factor
World Health Organization
radiation therapy
HMWK UPEP
HUS PI VIE
IBD PK VWD
IMF VWF
IMID PNH WHO
INR hemoglobinuria XRT
IPC prothrombin lime
Basics of Hematology
Hematopoietic Stem Cell
Erythrocyte:carries oxygen from lungs
to peripheral tissues
Reticulocyte:immature erythrocyte
Hb: protein contained in erythrocytes
which binds oxygen
Neutrophil: granulocyte integral in
innate immunity;main cell in acute
inflammation
Eosinophil:granulocyte involved
in response to parasites (especially
helminths) and allergic response
Basophil:granulocyte mainly involved in
allergy and parasitic infection
Lymphocyte:integral cell in adaptive
Immunity
Monocyte:involved in innate immunity:
can differentiate into macrophage or
dendritic cell
Platelet:mediator of primary hemostasis
Plasma:acellular,fluid component of
blood containing water and proteins
(including coagulation factors and
Immunoglobulins)
Serum:equivalent to plasma minus
coagulation factors
Myeloid piecursor Lymphoid precursor
Megakaryocyte/erythrocyte precursor
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Myeloblast Lymphoblast
Megakaryoblast Proerythroblast Monoblast
: Progranulocyte
Megakaryocyte Polychromatic
erythroblast
Monocyte
2
1
S
Basophil Eosinophil Neutrophil :
I
Erythrocyte Macrophage .1CJl
Platelets
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Granulocytes 0 r t
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Figure 1. Hematopoiesis
• over 101
'
blood cells arc produced daily
• sites ofhematopoiesis in adults: pelvis,sternum, vertebral bodies, and cranium
• lifespan of mature cells in blood
erythrocytes (90-120 d), neutrophils (~1 d), platelets (7-10 d),lymphocytes (varies- memory cells
pe rsist for years)
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H3 Hematology Toronto Notes 2023
• role of lymphoid organs
spleen: part of reticuloendothelial system, sequesters aged RBCs, removes opsonized cells, and
site of Ab production
thymus:site of T-cell maturation and involutes with age
• lymph nodes: sites of B- and T-cell activation (adaptive immune response)
Complete Blood Count
Table 1. Common Terms Found in the CBC
Test Definition Normal Values'
RBCCount Number of RBCs per volume of blood 3.5-5.0 x10l7L (female)
4.0-5.5 x 10RI (male)
115-155 9/1 (female)
125-170 g/L (male)
37-46% (female)
38-50% (male)
80100 ft
27-34 pg
315-355g/L
11.5-15.5%
23-90 x 1CP /L (0.5-1.5%)
<20 mm/h (female)
<10 mm/h (male)
3.5-10.5 X 103A
2 71 lOv.'
l
<0.7 x 1011
<0.10 *
1CP /L
<0.5x 109/1
1.0-4.0 x 101/1
0.1-1.0*
109 /1
130 380 x 109 /1
9.0-14.0 fl
Hb Amount olHbm the blood
Percentage of a given volume of whole blood occupied by packed
RBCs
Average RBC site
Average amount of Hb per RBCs
Average concentration of Hb inside RBCs
Percentage of variance in RBC size
Humber of reticulocytes per volume of blood
Rate at which RBCsseparate from the serum, becoming sediment in
the bottom of the test tube
Humber of WBCs per volume of blood
Segmented neutrophils
Band neutrophils
Basophils
Eosinophils
Lymphocytes
Monocytes
Humber of platelets pet volume of blood
Mean Platelet Volume (MPV ) Measurement ol plateletsize
Hct
MCV
MCH
MCHC
ROW
Reticulocyte Count
ESR
WBC Count
WBC Differential
Platelet Count
“All values apply to adults. Reference standards do not apply to all ethnic groups.
Approach to Interpreting a CBC
1 . consider values in the context of an individual'
s baseline:
up to 5% of population without disease may have values outside “normal" range
• an individual may display a clinically significant change from their baseline without violating
“normal"
reference range
2. is one cell line affected or are several?
• if all lines are low: pancytopenia (see Pancytopenia, HS )
if RBCs and platelets are low: consider a MAHA/TMA (see Microangiopathic Hemolytic Anemia/
thrombotic Microangiopathy, H23 ) or an autoimmune process (Evan’
s Syndrome)
• if single cell line affected: see Common Presenting Problems, H6
To estimate Hb based on the Hct,
multiply by 3
Clinical UseofRDW
. To distinguish the etiologies of
microcytosis:
• Iron deficiency:increased RDW
(anisocytosis) as cells are of varying
sizes in iron deficiency
• 3-thalassemia minor:normal RDV7
(also expect a high RBC count) as
cells are of similarsize because
the red cell abnormality is not
progressive
Blood Film Interpretation
RED BLOOD CELLS
Size
• microcytic (MCV <80 fL), normocvtic (MCV = 80-100 fL), macrocytic (MCV >100 fL)
• anisocytosis: RBCs with increased variability in size (increased RDW )
• iron deficiency anemia, HAs, Ml'
, blood transfusion, and MDS
Colour
• hypochromic: increase in size of central pallor (normal = less than 1/3 of RBC diameter)
iron deficiency anemia, anemia of chronic disease, and sideroblastic anemia
• polychromasia: suggests increased reticulocytes (pinkish-blue cells)
• increased RBC production by BM
Shape
• poikilocytosis: increased proportion of RBCs of abnormal shape
• iron deficiency anemia, hemoglobinopathies, ME, severe Bi:deficiency, MDS, and burns
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