Abstract |
Scleromyxedema is a rare dermatological disorder marked by widespread symmetric 2- to 3-mm, firm, waxy, closely spaced papules involving the hands, forearms, face, neck, upper trunk and thighs. The most common extracutaneous manifestation of scleromyxedema is a benign plasma cell dyscrasia. Treatment of scleromyxedema is limited by the lack of long-term results, toxicity and significant adverse side effects. We report a severe case of scleromyxedema who had marked improvement when treated with thalidomide.
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Authors | Sharon E Jacob, Sari Fien, Francisco A Kerdel |
Journal | Dermatology (Basel, Switzerland)
(Dermatology)
Vol. 213
Issue 2
Pg. 150-2
( 2006)
ISSN: 1018-8665 [Print] Switzerland |
PMID | 16902294
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright 2006 S. Karger AG, Basel. |
Chemical References |
- Angiogenesis Inhibitors
- Paraproteins
- Thalidomide
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Topics |
- Angiogenesis Inhibitors
(therapeutic use)
- Female
- Follow-Up Studies
- Humans
- Middle Aged
- Paraproteins
(drug effects, metabolism)
- Scleromyxedema
(blood, drug therapy)
- Severity of Illness Index
- Thalidomide
(therapeutic use)
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