Literature DB >> 9156861

Rhabdomyosarcoma of the biliary tree.

N Sanz1, L de Mingo, F Flórez, V Rollán.   

Abstract

Rhabdomyosarcoma (RMS) of the biliary tree is a rare tumor in children that has a very poor prognosis. Preoperatively, it is often mistaken for a choledochal cyst. We report a case of RMS of the biliary tree in a 4-year-old girl who presented with abdominal pain and obstructive jaundice. The RMS was diagnosed at laparotomy; excision was not possible due to its size and localization. Chemotherapy achieved complete regression of the tumor observed at second-look surgery. Preoperative chemotherapy can now avoid mutilating surgical procedures and improve survival.

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Year:  1997        PMID: 9156861

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  9 in total

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Journal:  Klin Padiatr       Date:  1986 May-Jun       Impact factor: 1.349

5.  Embryonal rhabdomyosarcoma of the ampulla of Vater with long-term survival following pancreaticoduodenectomy.

Authors:  M G Caty; K T Oldham; E V Prochownik
Journal:  J Pediatr Surg       Date:  1990-12       Impact factor: 2.545

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Journal:  Cancer       Date:  1988-01-15       Impact factor: 6.860

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Journal:  Cancer       Date:  1985-08-01       Impact factor: 6.860

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  9 in total
  2 in total

Review 1.  High-dose chemotherapy followed by autologous stem cell transplantation for metastatic rhabdomyosarcoma--a systematic review.

Authors:  Frank Peinemann; Nicolaus Kröger; Carmen Bartel; Ulrich Grouven; Max Pittler; Rudolf Erttmann; Michael Kulig
Journal:  PLoS One       Date:  2011-02-23       Impact factor: 3.240

2.  Hepatobiliary rhabdomyosarcoma mimicking choledochal cyst: Lessons learned.

Authors:  Mohamed Abd Elwahab; Hosam Hamed; Ahmed Shehta; Mahmoud Ali; Khaled Zalata
Journal:  Int J Surg Case Rep       Date:  2014-02-07
  2 in total

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