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Biliary dilatation secondary to lithiasis in a child affected by Langerhans' cell histiocytosis.

作者信息

Caruso Settimo, Miraglia Roberto, Spada Marco, Luca Angelo, Gridelli Bruno

机构信息

Department of Radiology, Mediterranean Institute for Transplantation and Advanced Specialized Therapies (IsMeTT), Palermo, Italy.

出版信息

J Clin Ultrasound. 2009 Jul-Aug;37(6):366-8. doi: 10.1002/jcu.20574.

Abstract

Langerhans' cell histiocytosis (LCH) is a disease of unknown pathogenesis, caused by clonal proliferation of Langerhans' cells. Liver involvement results in a cholangiopathy, which has the radiologic appearance of sclerosing cholangitis. Only 1 case of obstructive jaundice due to common bile duct stone in a patient with LCH has been described. We present a case of a 31-month-old child with LCH and liver involvement on the waiting list for liver transplantation. During the follow-up, there was a rapid onset of jaundice due to sludge and lithiasis. The patient was treated first with an endoscopic biliary plastic stent and then with percutaneous biliary drainage and bilioenteric anastomosis.

摘要

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