Reticulohistiocytoma
Medical condition
Reticulohistiocytoma | |
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Specialty | Dermatology |
Reticulohistiocytoma is a cutaneous condition characterized by a solitary, firm, dermal skin lesion of less than 1 cm in diameter.[1]: 718 It usually occurs in young adults or middle aged people, most commonly in females. Affected regions include the head and neck region and the upper part of the trunk. It may coexist with certain neoplasms or vasculitis, and in 30 percent of patients with xanthelasma.
See also
- Reticulohistiocytosis
- Non-X histiocytosis
References
- ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
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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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