X-type histiocytosis
Medical condition
| X-type histiocytosis | |
|---|---|
| Specialty | Dermatology |
X-type histiocytoses are a clinically well-defined group of cutaneous syndromes characterized by infiltrates of Langerhans cells, as opposed to Non-X histiocytosis in which the infiltrates contain monocytes/macrophages.[1]: 720 Conditions included in this group are:[1]: 720–4
- Congenital self-healing reticulohistiocytosis
- Langerhans cell histiocytosis
See also
- Non-X histiocytosis
- Histiocytosis
References
- ^ a b James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
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Histiocytosis
X-type histiocytosis
- Letterer–Siwe disease
- Hand–Schüller–Christian disease
- Eosinophilic granuloma
- Congenital self-healing reticulohistiocytosis
Non-X histiocytosis
- Juvenile xanthogranuloma
- Hemophagocytic lymphohistiocytosis
- Erdheim-Chester disease
- Niemann–Pick disease
- Sea-blue histiocytosis
- Benign cephalic histiocytosis
- Generalized eruptive histiocytoma
- Xanthoma disseminatum
- Progressive nodular histiocytosis
- Papular xanthoma
- Hereditary progressive mucinous histiocytosis
- Reticulohistiocytosis (Multicentric reticulohistiocytosis, Reticulohistiocytoma)
- Indeterminate cell histiocytosis
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