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Botryoid rhabdomyosarcoma of the biliary tract in children: a unique case report
Author(s) -
ZAMPIERI N.,
CAMOGLIO F.,
CORROPPOLO M.,
CECCHETTO M.,
ORNIS S.,
OTTOLENGHI A.
Publication year - 2006
Publication title -
european journal of cancer care
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 67
eISSN - 1365-2354
pISSN - 0961-5423
DOI - 10.1111/j.1365-2354.2006.00683.x
Subject(s) - medicine , rhabdomyosarcoma , choledochal cysts , biliary tract , radiological weapon , lesion , rare disease , disease , radiology , sarcoma , cyst , gastroenterology , surgery , pathology
Rhabdomyosarcoma (RMS) is the most common tumour of the biliary tree in childhood. In children, it is a rare lesion, accounting for about 1% of all RMS. Hepatobiliary botryoid RMS is a disease affecting young children at a median age of about 3 years. In literature, the radiological findings of hepatobiliary RMS have been described in small series and some case reports. In this case report, we present a rare case of RMS of the extrahepatic biliary tree initially diagnosed as a choledochal cyst.
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