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Liver transplantation for Langerhans' cell histiocytosis--a case report and literature review. 1996
H V Melendez, and
A Dhawan, and
G Mieli-Vergani, and
M Rela, and
N D Heaton, and
J Pritchard, and
A Mowat
Liver Transplant Surgical Service and Department of Child Health, King's College Hospital, London, United Kingdom.
Langerhans' cell histiocytosis (LCH) is a rare disorder of unknown etiology and pathogenesis. End-stage chronic liver disease is one presentation and orthotopic liver transplantation (OLT) has been reported in 17 cases, with variable resolution of LCH lesions postoperatively. We report a case of multisystem LCH with end-stage liver disease treated by OLT and review the overall results of OLT for children with LCH.
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