Xanthoma disseminatum: Difference between revisions
From WikiMD's Wellness Encyclopedia
CSV import |
CSV import Tag: Reverted |
||
| Line 53: | Line 53: | ||
{{stb}} | {{stb}} | ||
{{No image}} | {{No image}} | ||
__NOINDEX__ | |||
Revision as of 02:57, 18 March 2025
| Xanthoma disseminatum | |
|---|---|
| [[File:|250px|alt=|]] | |
| Synonyms | Disseminated xanthosiderohistiocytosis<ref name="Bolognia">{{{last}}},
Rapini, Ronald P., Dermatology: 2-Volume Set, St. Louis:Mosby, 2007, ISBN 978-1-4160-2999-1,</ref> and Montgomery syndrome<ref name="Andrews" /> |
| Pronounce | |
| Field | |
| Symptoms | |
| Complications | |
| Onset | |
| Duration | |
| Types | |
| Causes | |
| Risks | |
| Diagnosis | |
| Differential diagnosis | |
| Prevention | |
| Treatment | |
| Medication | |
| Prognosis | |
| Frequency | |
| Deaths | |
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.<ref name="Andrews">{{{last}}},
James, William D.,
Andrews' Diseases of the Skin: clinical Dermatology,
Saunders Elsevier,
2006,
ISBN 978-0-7216-2921-6,</ref>: 717
It is a histiocytosis syndrome.<ref name="pmid15681329">,
Xanthoma disseminatum: a case report and literature review, Br J Radiol, Vol. 78(Issue: 926), pp. 153–7, DOI: 10.1259/bjr/27500851, PMID: 15681329,</ref>
See also
References
<references group="" responsive="1"></references>
External links
| Inborn error of lipid metabolism: dyslipidemia (E78, 272.0–272.6) | ||||||||
|---|---|---|---|---|---|---|---|---|
|
| This article is a stub. You can help WikiMD by registering to expand it. |