## Abstract ## Objective To analyze features and outcomes of cholestasis, sclerosing cholangitis (SC), and liver transplantation (LTx) in patients with Langerhans cell Histiocytosis (LCH) between October 1987 and June 1999. ## Study design Of 182 cases with LCH, 36 had hepatic involvement and 12
Pediatric liver transplantation for langerhans' cell histiocytosis
β Scribed by Parissa Zandi; Yves Panis; Dominique Debray; Olivier Bernard; Didier Houssin
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 487 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0270-9139
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We report a case of Langerhans' cell histiocytosis (LCH) occurring after a living donor liver transplantation (LDLT) for fulminant hepatitis. A 9-month-old girl underwent an LDLT for fulminant hepatitis of an unknown cause. The histology of the native liver did not show any findings of LCH. On posto
Background. Treatment of multisystem Langerhans cell histiocytosis (LCH) remains difficult. Various regimens of single and multiagent chemotherapy have been used, but a significant proportion of patients fail to respond to treatment. Procedure. We have evaluated the use of cyclosporine A (CSA) in a