Non-Langerhans cell histiocytosis
From Infogalactic: the planetary knowledge core
Non-Langerhans cell histiocytosis | |
---|---|
Classification and external resources | |
Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
Patient UK | Non-Langerhans cell histiocytosis |
MeSH | D015616 |
Non-Langerhans cell histiocytosis refers to a family of histiocytosis characterized by the absence of Langerhans cells.[1]
Many manifest cutaneously.[2]
the spectrum of non-langerhans cell histiocytoses include:
- Benign cephalic histiocytosis
- Generalized eruptive histiocytoma
- Indeterminate cell histiocytosis
- Juvenile xanthogranuloma
- Progressive nodular histiocytoma
- Necrobiotic xanthogranuloma
- (Giant Cell) Reticulohistiocytoma
- Multicentric reticulohistiocytosis
- Rosai–Dorfman disease
- Xanthoma disseminatum
- Kikuchi disease
- Erdheim–Chester disease.[3]
References
<templatestyles src="Asbox/styles.css"></templatestyles>