Xanthoma disseminatum
| Xanthoma disseminatum | |
|---|---|
| Other names | Disseminated xanthosiderohistiocytosis[1] and Montgomery syndrome[2] |
| Specialty | Endocrinology  |
Xanthoma disseminatum 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[]
- Non-X histiocytosis
- List of cutaneous conditions
References[]
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
- ^ a b James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
- ^ 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. doi:10.1259/bjr/27500851. PMID 15681329.
External links[]
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- Monocyte- and macrophage-related cutaneous conditions
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