Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.

Cholestasis

Impairment of bile flow due to obstruction in bile ducts.


合計: 2

                       


（表示件数）
PMID (PMCID)
25859497
 OTHER
Disseminated langerhans cell histiocytosis presenting as cholestatic jaundice.
Kapoor R, Loizides AM, Sachdeva S, Paul P.
J Clin Diagn Res. 2015;9(2):SD03-5.
In this report, we describe a case of type II histiocytosis X with obstructive cholestasis and pulmonary involvement in the form of cysts without significant lymphadenopathy at the porta.
2344248
 MALE
[Sclerosing cholangitis revealing histiocytosis X].
Neveu I, Labrune P, Huguet P, Musset D, Chaussain JL, Odievre M.
Arch Fr Pediatr. 1990;47(3):197-9.
The case of a 3 year-old boy who presented isolated cholestasis as the initial symptom of histiocytosis X is described.