Epidemiology
congenital Langerhans cell histiocytosis (rare)
Ultrastructure
Localization
skin
digestive system
lymph node
liver
female genital tract (12801274)
Variants
malignant Langerhans cell tumor (11437944, 12963924)
Immunochemistry
CD1a+
S100+
CD68-
fascine+
CGH
losses of DNA sequences on chromosomes 1p, 5, 6, 7, 9, 16, 17, and 22q (12094383)
gain of DNA copy number was seen on chromosomes 2q, 4q, and 12 (12094383)
LOH (17378622)
1p LOH (12094383)
5q23 LOH (17378622)
Chr.7 LOH (12094383)
Chr.9 LOH (12094383)
22q LOH (12094383)
Case records
Case 11335: Femoral Langerhans histiocytosis
Case 12691: Faciocranial Langerhans cell histiocytosis
References
Chikwava KR, Hunt JL, Mantha GS, Murphy JE, Jaffe R. Analysis of loss of heterozygosity in single-system and multisystem langerhans’ cell histiocytosis. Pediatr Dev Pathol. 2007 Jan-Feb;10(1):18-24. PMID: 17378622
Murakami I, Gogusev J, Fournet JC, Glorion C, Jaubert F. Detection of molecular cytogenetic aberrations in langerhans cell histiocytosis of bone. Hum Pathol. 2002 May;33(5):555-60. PMID: 12094383