Severe sclerosing cholangitis after Langerhans cell histiocytosis treated by liver transplantation: An adult case report

Langerhans cell histiocytosis (LCH) is a rare hematopoietic disorder of unknown pathogenesis. LCH diseases may occur in a single organ or multisystem organ. The patients with multisystem involvement usually have a poor prognosis. Liver involvement in multisystem LCH results in severe complications,...

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Veröffentlicht in:	Medicine (Baltimore) 2017-03, Vol.96 (9), p.e5994-e5994
Hauptverfasser:	Tang, Yunhua, Zhang, Zhiheng, Chen, Maogen, Ju, Weiqiang, Wang, Dongping, Ji, Fei, Ren, Qingqi, Guo, Zhiyong, He, Xiaoshun
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Cholangitis, Sclerosing - etiology Cholangitis, Sclerosing - surgery Clinical Case Report Histiocytosis, Langerhans-Cell - complications Humans Liver Transplantation Male
Online-Zugang:	Volltext
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