- Xanthoma disseminatum
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Xanthoma disseminatum Classification and external resources ICD-10 E78.2 (ILDS E78.240) Xanthoma disseminatum (also known as "Disseminated xanthosiderohistiocytosis"[1] and "Montgomery syndrome"[2]) is a rare cutaneous condition that preferentially affects males in childhood, characterized by the insidious onset of small, yellow-red to brown papules and nodules that are discrete and disseminated.[2]:717
It is a histiocytosis syndrome.[3]
See also
References
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ^ 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.
- ^ Alexander AS, Turner R, Uniate L, Pearcy RG (February 2005). "Xanthoma disseminatum: a case report and literature review". Br J Radiol 78 (926): 153–7. PMID 15681329.
Lipodystrophy Other 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 Categories:- Cutaneous condition stubs
- Monocyte- and macrophage-related cutaneous conditions
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