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.

Anemia

A reduction in erythrocytes volume or hemoglobin concentration.


合計: 2

                       


（表示件数）
PMID (PMCID)
27621925
(5004507)
 OTHER
Pericardial Effusion in Langerhans Cell Histiocytosis: A Case Report.
Gholami N.
Iran Red Crescent Med J. 2016;18(6):e25604.
Langerhans cell histiocytosis was suspected when it was associated with anemia, splenomegaly and lytic bone lesions.
17030599
 FEMALE Infant
Gastrointestinal tract involvement in Langerhans cell histiocytosis: case report and literature review.
Hait E, Liang M, Degar B, Glickman J, Fox VL.
Pediatrics. 2006;118(5):e1593-9.
We report a case of Langerhans cell histiocytosis in an otherwise thriving neonate presenting with hematochezia, anemia, and rash.