- Multicentric reticulohistiocytosis
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Multicentric reticulohistiocytosis is a multisystem disease beginning usually around the age of 50 years old, and is twice as common in women.[1]:718[2]
See also
- Reticulohistiocytosis
- List of cutaneous conditions
References
Histiocytosis (D76.0, 277.89) WHO-I/Langerhans cell histiocytosis/
X-type histiocytosisLetterer–Siwe disease · Hand–Schüller–Christian disease · Eosinophilic granuloma · Congenital self-healing reticulohistiocytosisWHO-II/non-Langerhans cell histiocytosis/
Non-X histiocytosisJuvenile xanthogranuloma · Hemophagocytic lymphohistiocytosis · Erdheim-Chester disease · Niemann-Pick disease · Sea-blue histiocyte syndrome · Benign cephalic histiocytosis · Generalized eruptive histiocytoma · Xanthoma disseminatum · Progressive nodular histiocytosis · Papular xanthoma · Hereditary progressive mucinous histiocytosis · Reticulohistiocytosis (Multicentric reticulohistiocytosis, Reticulohistiocytoma) · Indeterminate cell histiocytosisWHO-III/malignant histiocytosis Histiocytic sarcoma · Langerhans cell sarcoma · Interdigitating dendritic cell sarcoma · Follicular dendritic cell sarcomaUngrouped This cutaneous condition article is a stub. You can help Wikipedia by expanding it.