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.

Hepatosplenomegaly

Simultaneous enlargement of the liver and spleen.


合計: 2

                       


（表示件数）
PMID (PMCID)
21695102
(3117631)
 OTHER
Neonatal systemic juvenile xanthogranuloma with an ominous presentation and successful treatment.
Fan R, Sun J.
Clin Med Insights Oncol. 2011;5:157-61.
The patient presented with blue muffin rush, cervical mass, bone destruction, lung nodule, hepatosplenomegaly, and coagulopathy and was successfully treated with Langerhans cell histiocytosis (LCH) based chemotherapy treatment.
1291759
 FEMALE
A case of hypersensitivity syndrome resembling Langerhans cell histiocytosis during phenobarbital prophylaxis for convulsion.
Nagata T, Kawamura N, Motoyama T, Miyake M, Yoden A, Yoshikawa K, Oguni T, Yamasiro K, Mino M.
Jpn J Clin Oncol. 1992;22(6):421-7.
Symptoms, including intermittent fever, systemic lymphadenopathy, maculopapular skin eruption and hepatosplenomegaly, suggested Langerhans cell histiocytosis.