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MRI误诊小儿胆管胚胎性横纹肌肉瘤并文献复习 被引量:5

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摘要 目的分析小儿胆管胚胎性横纹肌肉瘤的误诊原因并提出防范对策,以降低误诊率。方法对我院收治并经MRI误诊的1例小儿胆管胚胎性横纹肌肉瘤的临床资料进行回顾性分析并结合相关文献进行复习。结果本例因腹痛10d,全身皮肤黄染8d就诊,根据临床症状、体征结合MRI、磁共振胰胆管水成像(MRCP)及其增强扫描,诊断为先天性胆管囊肿并慢性感染,行手术治疗,术后病理诊断为胆管胚胎性横纹肌肉瘤(葡萄簇亚型),患儿5个月后死亡。结论小儿胆管胚胎性横纹肌肉瘤临床罕见,有效融合多种MRI成像序列辅以多方位成像检查,熟悉横纹肌肉瘤的病理学特性,结合病变中高度强化特性,可提高本病的确诊率。
出处 《临床误诊误治》 2012年第4期103-104,共2页 Clinical Misdiagnosis & Mistherapy
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  • 1王建文.小儿横纹肌肉瘤[J].实用儿科临床杂志,2005,20(1):6-7. 被引量:15
  • 2刘卓炜,周芳坚,秦自科,韩辉,余绍龙,王欢.成人前列腺肉瘤6例治疗报告(附文献复习)[J].癌症,2005,24(2):226-228. 被引量:5
  • 3李巍松,施诚仁.儿童软组织肉瘤的化疗[J].临床外科杂志,2005,13(5):321-323. 被引量:4
  • 4张惜阴.宫颈上皮内瘤样病变.临床妇科肿瘤学[M].上海:上海医科大学出版社,1992.89-95.
  • 5Chui CH,Billups CA,Pappo AS,et al.Prediction of outcome in chilfren and abdolesceents with rhabdommyosarcoma of the St,Jude Chilgren Research Hospital experience[J].J Pdiatr Surg,2005,40(11):1691-1695.
  • 6Maurer H M, Gehan E A, Beltangady M, et al. The Intergroup Ghabdom yo sarcoma Study-II[J]. Cancer, 1993, 71 (5) : 1904-1922.
  • 7Maurer HM, Gehan EA, Beltangady M, et al. The Intergroup Rhabdomyosarcoma Study-ll[J]. Cancer, 1993, 71(5) : 1904- 1922.
  • 8Crist W, Gehan EA, Ragab AH, et al. The third Intergroup Rhab domyosareoma Study[J]. J Clin Oncol, 1995, 13(3) : 610-630.
  • 9Crist WM, Anderson JR, Meza JL, et al. Intergroup rhabdomyosar coma study-IV: Results for patients with nonmetastatic disease[J]. J Clin Oncol, 2001, 19(12): 3091-3102.
  • 10Alvarez Silvdn AM, Garcia Cant6n JA, Pineda Cuevas G, et al. Suc cessful treatment of orbital rhabdomyosarcoma in 2 infants using chemotherapy alone[J]. Med Ped Oncol, 1996, 26 (3) : 186-189.

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  • 1何乐健,王琳,孙宁,黄澄如,祝秀丹,郎志奇.儿童横纹肌肉瘤的临床病理研究[J].中华病理学杂志,2004,33(3):225-228. 被引量:40
  • 2Magn N, Haie-Meder C. B rachy therapy for genital tract rhabdomyosarcomas in girls: technical aspects, reports, and perspectives. Lancet Oncol,2007,8(8): 725-729.
  • 3吴晔明.小儿外科原则.第2版.北京:大学医学出版社,2004:5.
  • 4Yang J, Codreanu I, Servaes S, et al. Metastatic embryonal rhabdomyosarcoma to the pancreas presenting as acutepancreatitis detected by FDG PET/CT. Clin Nucl Med, 2/)I 2, 37(7) :694-696.
  • 5Spunt SL, LobeTE, PappoAS, et al. Aggressive surgery is unwarranted for biliary tract rhabdomyosaeoma. J Pediatr Surg,2000, 35(2) :309.
  • 6Scherzinger-LaudeK, Sch6nherr C, Lewrick F, et al. Treatment of neuroblastoma and rhabdomyosarcoma using RGD-modified liposomal formulations of patupilone (EPO906). Int J Nanomedicine, 2013,8 : 2197-2211.
  • 7Ruymann FB, Raney RB Jr, Crist WN, et al. Rhabdomyosarcoma of the biliary tree in childhood. A report from the Intergroup Rhabdomyosarcoma Study[J]. Cancer, 1985,56(3): 575-581.
  • 8Spunt SL, Lobe TE, Pappo AS, et al. Aggressive surgery is unwarranted for biliary tract rhabdomyosacoma[J]. J Pediatr Surg,2000,35(2) :309-316.
  • 9Balkan E, Kiristioglu I, Gtirpinar A, et al. Rhabdomyosarcoma of the biliary tree[J]. Turk J Pediatr, 1999,41(2):245-248.
  • 10Elwahab MA, Hamed H, Shehta A, et al. Hepatobiliary rhabdomyosareoma mimicking choledochal cyst=lessons learned [J]. Int J Surg Case Rep, 2014,5(4) : 196-199.

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