Search This Blog

Translate

خلفيات وصور / wallpapers and pictures images / fond d'écran photos galerie / fondos de pantalla en i

Buscar este blog

10/30/25

 


174. Crist WM, Anderson JR, Meza JL, et al. Intergroup rhabdomyosarcoma study-IV: results for

patients with nonmetastatic disease. J Clin Oncol 2001;19(12):3091–3102.

175. Arndt CA, Stoner JA, Hawkins DS, et al. Vincristine, actinomycin, and cyclophosphamide compared

with vincristine, actinomycin, and cyclophosphamide alternating with vincristine, topotecan, and

cyclophosphamide for intermediate-risk rhabdomyosarcoma: Children’s Oncology Group Study

D9803. J Clin Oncol 2009;27(31):5182–5188.

176. Soft Tissue Sarcoma Committee of the Children’s Oncology Group; Lager JJ, Lyden ER, Anderson

JR, et al. Pooled analysis of phase II window studies in children with contemporary high-risk

metastatic rhabdomyosarcoma: a report from the Soft Tissue Sarcoma Committee of the Children’s

Oncology Group. J Clin Oncol 2006;24(21):3415–3422.

177. Weigel B, Lyden E, Anderson JR, et al. Early results from Children’s Oncology Group (COG)

ARST0431: intensive multidrug therapy for patients with metastatic rhabdomyosarcoma (RMS).

ASCO Meeting Abstracts 2010;28(15 suppl):9503.

178. Malempati S, Weigel B, Anderson JR, et al. Early results from Children’s Oncology Group (COG)

ARST08P1: pilot studies of cixutumumab or temozolomide with intensive multiagent chemotherapy

for patients with metastatic rhabdomyosarcoma (RMS). ASCO Meeting Abstracts 2015; 33(15

suppl):10015.

179. Paulino AC, Okcu MF. Rhabdomyosarcoma. Curr Probl Cancer 2008; 32(1):7–34.

180. Donaldson SS, Meza J, Breneman JC, et al. Results from the IRS-IV randomized trial of

hyperfractionated radiotherapy in children with rhabdomyosarcoma—a report from the IRSG. Int J

Radiat Oncol Biol Phys 2001;51(3):718–728.

181. Linabery AM, Ross JA. Trends in childhood cancer incidence in the U.S. (1992–2004). Cancer

2008;112(2):416–432.

182. Sultan I, Casanova M, Al-Jumaily U, et al. Soft tissue sarcomas in the first year of life. Eur J Cancer

2010;46(13):2449–2456.

183. Kleinerman RA, Tucker MA, Abramson DH, et al. Risk of soft tissue sarcomas by individual subtype

in survivors of hereditary retinoblastoma. J Natl Cancer Inst 2007;99(1):24–31.

184. S⊘rensen SA, Mulvihill JJ, Nielsen A. Long-term follow-up of von Recklinghausen

neurofibromatosis. N Engl J Med 1986;314(16):1010–1015.

185. Strahm B, Malkin D. Hereditary cancer predisposition in children: genetic basis and clinical

implications. Int J Cancer 2006;119(9):2001–2006.

186. Spunt SL, Skapek SX, Coffin CM. Pediatric nonrhabdomyosarcoma soft tissue sarcomas. Oncologist

2008;13(6):668–678.

187. Haldar M, Hancock JD, Coffin CM, et al. A conditional mouse model of synovial sarcoma: insights

into a myogenic origin. Cancer Cell 2007; 11(4):375–388.

188. Duyster J, Bai RY, Morris SW. Translocations involving anaplastic lymphoma kinase (ALK).

Oncogene 2001;20(40):5623–5637.

189. Maire G, Fraitag S, Galmiche L, et al. A clinical, histologic, and molecular study of 9 cases of

congenital dermatofibrosarcoma protuberans. Arch Dermatol 2007;143(2):203–210.

190. Pappo AS, Rao BN, Jenkins JJ, et al. Metastatic nonrhabdomyosarcomatous soft tissue sarcomas in

children and adolescents: the St. Jude Children’s Research Hospital experience. Med Pediatr Oncol

1999;33(2):76–82.

191. West RB, van de Rijn M. The role of microarray technologies in the study of soft tissue tumours.

Histopathology 2006;48(1):22–31.

192. Parham DM, Webber BL, Jenkins JJ, et al. Nonrhabdomyosarcomatous soft tissue sarcomas of

childhood: formulation of a simplified system for grading. Mod Pathol 1995;8(7):705–710.

193. Hayes-Jordan A. Recent advances in non-rhabdomyosarcoma soft-tissue sarcomas. Semin Pediatr

Surg 2012;21(1):61–67.

194. Ferrari A, Miceli R, Meazza C, et al. Soft tissue sarcomas of childhood and adolescence: the

prognostic role of tumor size in relation to patient body size. J Clin Oncol 2009;27(3):371–376.

195. Hawkins DS, Spunt SL, Skapek SX. Children’s Oncology Group’s 2013 blueprint for research: soft

tissue sarcomas. Pediatr Blood Cancer 2013;60(6):1001–1008.

196. Maduekwe UN, Hornicek FJ, Springfield DS, et al. role of sentinel lymph node biopsy in the staging

of synovial, epithelioid, and clear cell sarcomas. Ann Surg Oncol 2009;16(5):1356–1363.

3114

197. Kayton ML, Delgado R, Busam K, et al. Experience with 31 sentinel lymph node biopsies for

sarcomas and carcinomas in pediatric patients. Cancer 2008;112(9):2052–2059.

198. Spector LG, Birch J. The epidemiology of hepatoblastoma. Pediatr Blood Cancer 2012;59(5):776–

779.

199. Feusner J, Plaschkes J. Hepatoblastoma and low birth weight: a trend or chance observation? Med

Pediatr Oncol 2002;39(5):508–509.

200. Trobaugh-Lotrario AD, Venkatramani R, Feusner JH. Hepatoblastoma in children with Beckwith–

Wiedemann syndrome: does it warrant different treatment? J Pediatr Hematol Oncol

2014;36(5):369–373.

201. Sparago A, Russo S, Cerrato F, et al. Mechanisms causing imprinting defects in familial Beckwith–

Wiedemann syndrome with Wilms’ tumour. Hum Mol Genet 2007;16(3):254–264.

202. Mamlok V, Nichols M, Lockhart L, et al. Trisomy 18 and hepatoblastoma. Am J Med Genet

1989;33(1):125–126.

203. Hughes LJ, Michels VV. Risk of hepatoblastoma in familial adenomatous polyposis. Am J Med Genet

1992;43(6):1023–1025.

204. Tan ZH, Lai A, Chen CK, et al. Association of trisomy 18 with hepatoblastoma and its implications.

Eur J Pediatr 2014;173(12):1595–1598.

205. Tonk VS, Wilson KS, Timmons CF, et al. Trisomy 2, trisomy 20, and del(17p) as sole chromosomal

abnormalities in three cases of hepatoblastoma. Genes Chromosomes Cancer 1994;11(3):199–202.

206. Albrecht S, Schweinitz von D, Waha A, et al. Loss of maternal alleles on chromosome arm 11p in

hepatoblastoma. Cancer Res 1994;54(19):5041–5044.

207. Hartmann W, Waha A, Koch A, et al. p57KIP2 is not mutated in hepatoblastoma but shows

increased transcriptional activity in a comparative analysis of the three imprinted genes p57KIP2,

IGF2, and H19. Am J Pathol 2000;157(4):1393–1403.

208. Kraus JA, Albrecht S, Wiestler OD, et al. Loss of heterozygosity on chromosome 1 in human

hepatoblastoma. Int J Cancer 1996;67(4):467–471.

209. Tomlinson GE, Douglass EC, Pollock BH, et al. Cytogenetic evaluation of a large series of

hepatoblastomas: numerical abnormalities with recurring aberrations involving 1q12-q21. Genes

Chromosomes Cancer 2005;44(2):177–184.

210. Ruck P, Xiao J-C. Stem-like cells in hepatoblastoma. Med Pediatr Oncol 2002;39(5):504–507.

211. Fiegel HC, Glüer S, Roth B, et al. Stem-like cells in human hepatoblastoma. J Histochem Cytochem

2004;52(11):1495–1501.

212. Gonzalez-Crussi F, Upton MP, Maurer HS. Hepatoblastoma: attempt at characterization of

histologic subtypes. Am J Surg Pathol 1982;6(7):599.

213. Czauderna P, Lopez-Terrada D, Hiyama E, et al. Hepatoblastoma state of the art: pathology,

genetics, risk stratification, and chemotherapy. Curr Opin Pediatr 2014;26(1):19–28.

214. Haas JE, Muczynski KA, Krailo M, et al. Histopathology and prognosis in childhood hepatoblastoma

and hepatocarcinoma. Cancer 1989;64(5):1082–1095.

215. Trobaugh-Lotrario AD, Tomlinson GE, Finegold MJ, et al. Small cell undifferentiated variant of

hepatoblastoma: adverse clinical and molecular features similar to rhabdoid tumors. Pediatr Blood

Cancer 2009;52(3):328–334.

216. Meyers RL, Rowland JR, Krailo M, et al. Predictive power of pretreatment prognostic factors in

children with hepatoblastoma: a report from the Children’s Oncology Group. Pediatr Blood Cancer

2009;53(6):1016–1022.

217. Schweinitz DV, Hadam MR, Welte K. Production of interleukin-1β and interleukin-6 in

hepatoblastoma. Int J Cancer 1993;53:72–734.

218. Schweinitz von D, Faundez A, Teichmann B, et al. Hepatocyte growth-factor-scatter factor can

stimulate post-operative tumor-cell proliferation in childhood hepatoblastoma. Int J Cancer

2000;85(2):151–159.

219. Perilongo G, Brown J, Shafford E, et al. Hepatoblastoma presenting with lung metastases. Cancer

2000;89(8):1845–1853.

220. Meyers RL. Tumors of the liver in children. Surg Oncol 2007;16(3):195–203.

221. Katzenstein HM, Krailo MD, Malogolowkin MH, et al. Hepatocellular carcinoma in children and

3115

adolescents: results from the Pediatric Oncology Group and the Children’s Cancer Group intergroup

study. J Clin Oncol 2002;20(12):2789–2797.

222. Brown J, Perilongo G, Shafford E, et al. Pretreatment prognostic factors for children with

hepatoblastoma—results from the International Society of Paediatric Oncology (SIOP) study

SIOPEL 1. Eur J Cancer 2000;36(11):1418–1425.

223. Aronson DC, Schnater JM, Staalman CR, et al. Predictive value of the pretreatment extent of

disease system in hepatoblastoma: results from the International Society of Pediatric Oncology

Liver Tumor Study Group SIOPEL-1 study. J Clin Oncol 2005;23(6):1245–1252.

224. Schweinitz von D, Hecker H, Harms D, et al. Complete resection before development of drug

resistance is essential for survival from advanced hepatoblastoma—a report from the German

Cooperative Pediatric Liver Tumor Study HB-89. J Pediatr Surg 1995;30(6):845–852.

225. Lovvorn HN III, Ayers D, Zhao Z, et al. Defining hepatoblastoma responsiveness to induction

therapy as measured by tumor volume and serum α-fetoprotein kinetics. J Pediatr Surg

2010;45(1):121–129.

226. Taylor PH, Filler RM, Nebesar RA, et al. Experience with hepatic resection in childhood. Am J Surg

1969;117(4):435–441.

227. Lee CS, Sung JL, Hwang LY, et al. Surgical treatment of 109 patients with symptomatic and

asymptomatic hepatocellular carcinoma. Surgery 1986;99(4):481–490.

228. Exelby PR, Filler RM, Grosfeld JL. Liver tumors in children in the particular reference to

hepatoblastoma and hepatocellular carcinoma: American Academy of Pediatrics Surgical Section

Survey 1974. J Pediatr Surg 1975;10(3):329–337.

229. Malogolowkin MH, Katzenstein HM, Meyers RL, et al. Complete surgical resection is curative for

children with hepatoblastoma with pure fetal histology: a report from the Children’s Oncology

Group. J Clin Oncol 2011;29(24):3301–3306.

230. Ortega JA, Douglass EC, Feusner JH, et al. Randomized comparison of

cisplatin/vincristine/fluorouracil and cisplatin/continuous infusion doxorubicin for treatment of

pediatric hepatoblastoma: a report from the Children’s Cancer Group and the Pediatric Oncology

Group. J Clin Oncol 2000;18(14):2665–2675.

231. Habrand JL, Nehme D, Kalifa C, et al. Is there a place for radiation therapy in the management of

hepatoblastomas and hepatocellular carcinomas in children? Int J Radiat Oncol Biol Phys

1992;23(3):525–531.

232. Koneru B, Flye MW, Busuttil RW, et al. Liver transplantation for hepatoblastoma. The American

experience. Ann Surg 1991;213(2):118–121.

233. Faraj W, Dar F, Marangoni G, et al. Liver transplantation for hepatoblastoma. Liver Transpl

2008;14(11):1614–1619.

234. Tiao GM, Bobey N, Allen S, et al. The current management of hepatoblastoma: a combination of

chemotherapy, conventional resection, and liver transplantation. J Pediatr 2005;146(2):204–211.

235. Moon SB, Shin HB, Seo JM, et al. Hepatoblastoma: 15-year experience and role of surgical

treatment. J Korean Surg Soc 2011;81(2):134–140.

236. Meyers RL, Tiao G, de Ville de Goyet J, et al. Hepatoblastoma state of the art: pre-treatment extent

of disease, surgical resection guidelines and the role of liver transplantation. Curr Opin Pediatr

2014;26(1):29–36.

237. Austin MT, Leys CM, Feurer ID, et al. Liver transplantation for childhood hepatic malignancy: a

review of the United Network for Organ Sharing (UNOS) database. J Pediatr Surg 2006;41(1):182–

186.

238. Otte J-B, de V de Goyet J, Reding R. Liver transplantation for hepatoblastoma: indications and

contraindications in the modern era. Pediatr Transpl 2005;9(5):557–565.

239. Trobaugh-Lotrario AD, Katzenstein HM. Chemotherapeutic approaches for newly diagnosed

hepatoblastoma: past, present, and future strategies. Pediatr Blood Cancer 2012;59(5):809–812.

240. Jacobs JF, Coulie PG, Figdor CG, et al. Targets for active immunotherapy against pediatric solid

tumors. Cancer Immunol Immunother 2009;58(6):831–841.

241. Czauderna P, Mackinlay G, Perilongo G, et al. Hepatocellular carcinoma in children: results of the

first prospective study of the International Society of Pediatric Oncology group. J Clin Oncol

2002;20(12):2798–2804.

3116

242. Otte JB, de Ville de Goyet J. The contribution of transplantation to the treatment of liver tumors in

children. Semin Pediatr Surg 2005;14(4):233–238.

243. Malogolowkin MH, Stanley P, Steele DA, et al. Feasibility and toxicity of chemoembolization for

children with liver tumors. J Clin Oncol 2000; 18(6):1279–1284.

3117

Chapter 106

The Pregnant Patient

Juan L. Martinez-Poyer and N. Scott Adzick

Key Points

1 One of the most significant advances in the reduction of morbidity of prematurity has been the use

of antenatal corticosteroids.

2 To accommodate the fetus, placenta, and amniotic fluid, the uterus increases in size and weight and

its walls become thinner. By the end of the first trimester, the uterus moves out of the pelvis and by

20 weeks reaches the level of the umbilicus. By term, it almost reaches the liver.

3 The etiology of preterm labor is often multifactorial, but the onset of labor from fetal and uterine

stress from surgical manipulation is of most concern to the surgeon.

4 Initiation of tocolytic therapy for potential but unconfirmed preterm labor is discouraged.

5 Exposure to diagnostic levels of radiation carries little chance for spontaneous abortion,

teratogenesis, or growth retardation. The increased risk of future cancer, however, does exist and

must be weighted against the utility of information provided by the study.

6 Attributing abdominal pain to other etiologies, failure to pursue further investigation, and the

physicians’ fear of surgically induced premature labor all contribute to delayed diagnosis, higher

perforation rates, diffuse peritonitis, preterm labor, and fetal loss in pregnant patients with

appendicitis.

7 Cholecystectomy can be performed safely and effectively during pregnancy in all trimesters.

Nonoperative management of symptomatic cholelithiasis is associated with significant recurrent

bouts of symptoms, prolonged total parenteral nutrition, higher rates of preterm delivery, cesarean

section, and more technically difficult cholecystectomies.

8 Adhesions remain the most common cause of intestinal obstruction in the gravid patient, with 89%

to 100% of patients eventually requiring an operation.

9 Pregnant patients present with more advanced colorectal cancers than the population a whole. The

necessary treatment must balance oncology outcomes with effect on the pregnancy, and decisions

regarding the management of pregnancy include termination, iatrogenic prematurity, or intentional

delay in treatment.

The general surgeon at some point in his or her career will be asked to operate on an obstetrical patient

or be urgently consulted for intraoperative assistance with an unanticipated surgical finding or

complication. To provide the best support, it is imperative that he or she is knowledgeable of the

normal physiologic variations occurring during pregnancy, the frequency and nature of presentation of

surgical disease, the safety and utility of diagnostic imaging modalities, and the newest surgical

techniques to ensure the safety and well-being of the mother and the fetus. To achieve this goal, the

concerted effort and close working relationship between various specialties cannot be overemphasized.

This chapter reviews the current data on the presentation, frequency, and treatment of some common

surgical diseases during gestation, as well as their impact on pregnancy.

FETAL DEVELOPMENT

1 Human development begins immediately on fertilization of the oocyte by the sperm, but because in

many cases it is very difficult to determine the exact time of fertilization, pregnancy is generally dated

from the first day of the last menstrual period. However, dating using menstrual age is less accurate

than early ultrasonography dating because of reliance on recall, cycle length variability, and pregnancy

after cessation of oral contraceptives or following childbirth.1,2 Ultrasonography provides a better

estimate of the date of delivery than a reliable last menstrual period before 20 weeks of gestation, with

3118

No comments:

Post a Comment

اكتب تعليق حول الموضوع

Popular Posts

Popular Posts

Popular Posts

Popular Posts

Translate

Blog Archive

Blog Archive

Featured Post

  ABSTRACT Doxorubicin (Dox) is a highly potent chemotherapy drug. Despite its efficacy, Dox's clinical application is limited due to it...