Document Detail


Liver transplantation in Langerhans' cell histiocytosis (histiocytosis X).
MedLine Citation:
PMID:  1992520     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Two children with biopsy-proven LCH underwent successful hepatic transplantation for end-stage liver disease. These patients were thought not to have active LCH disease at the time of transplantation, although one had developed a new osteolytic lesion a few months before the operation and the other had suspicious osteolytic lesions at the time of transplantation. The histologic examination of the excised liver showed features consistent with primary sclerosing cholangitis. The two patients had an excellent recovery with no evidence of progression of LCH or recurrence of the underlying disease in the hepatic allograft at 1 and 3 years after organ transplantation.
Authors:
W Concepcion; C O Esquivel; A Terry; P Nakazato; R Garcia-Kennedy; D Houssin; K L Cox
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Seminars in oncology     Volume:  18     ISSN:  0093-7754     ISO Abbreviation:  Semin. Oncol.     Publication Date:  1991 Feb 
Date Detail:
Created Date:  1991-03-11     Completed Date:  1991-03-11     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0420432     Medline TA:  Semin Oncol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  24-8     Citation Subset:  IM    
Affiliation:
Division of Transplantation, Pacific Presbyterian Medical Center, San Francisco, CA 94115.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Child, Preschool
Female
Histiocytosis, Langerhans-Cell / complications,  surgery*
Humans
Liver Transplantation*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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