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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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| Publicat a: | Medicine (Baltimore) |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer Health
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5340431/ https://ncbi.nlm.nih.gov/pubmed/28248858 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000005994 |
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