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

BACKGROUND: 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 com...

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Detalles Bibliográficos
Autores principales: Tang, Yunhua, Zhang, Zhiheng, Chen, Maogen, Ju, Weiqiang, Wang, Dongping, Ji, Fei, Ren, Qingqi, Guo, Zhiyong, He, Xiaoshun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
7100
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340431/
https://www.ncbi.nlm.nih.gov/pubmed/28248858
http://dx.doi.org/10.1097/MD.0000000000005994

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340431/
https://www.ncbi.nlm.nih.gov/pubmed/28248858
http://dx.doi.org/10.1097/MD.0000000000005994

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