Literature DB >> 19280659

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

Settimo Caruso1, Roberto Miraglia, Marco Spada, Angelo Luca, Bruno Gridelli.   

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.

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Year:  2009        PMID: 19280659     DOI: 10.1002/jcu.20574

Source DB:  PubMed          Journal:  J Clin Ultrasound        ISSN: 0091-2751            Impact factor:   0.910


  3 in total

Review 1.  Langerhans cell histiocytosis and choledocholithiasis: is there an association?

Authors:  Udayakumar Navaneethan; Mansour A Parsi
Journal:  Gastroenterol Hepatol (N Y)       Date:  2012-11

2.  Langerhans cell histiocytosis and choledocholithiasis: a causal relationship or coincidence?

Authors:  Arunkumar Krishnan; Ravi Ramakrishnan; Jayanthi Venkataraman
Journal:  Gastroenterol Hepatol (N Y)       Date:  2012-11

3.  Disseminated langerhans cell histiocytosis presenting as cholestatic jaundice.

Authors:  Rohit Kapoor; Anthony M Loizides; Soumya Sachdeva; Premila Paul
Journal:  J Clin Diagn Res       Date:  2015-02-01
  3 in total

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