Abstract | STUDY OBJECTIVES: DESIGN: SETTING: Patients were seen at one of four specialized sarcoidosis clinics in the United States. PATIENTS: INTERVENTIONS: Skin lesions were assessed with visual examination by the treating physician, and photographic evaluation by a blinded panel of physicians reviewing photographs of the lesions before and after therapy. MEASUREMENTS AND RESULTS: Fourteen patients completed 4 months of therapy. All patients experienced some improvement in their skin lesions subjectively, and 10 of 12 evaluable patients showed improvement using photograph scoring. Five patients were better after 1 month (treated with 50 mg/d of thalidomide), seven more patients improved after 2 months (treated with 100 mg/d of thalidomide in the second month), and two patients required an additional month of 200 mg of thalidomide to achieve a response. Patients reported increased somnolence (n = 9), numbness (n = 7), dizziness (n = 2), constipation (n = 6), rash (n = 1), and increasing shortness of breath (n = 1). One patient discontinued therapy because of new-onset dyspnea, due to probably unrelated new-onset congestive heart failure. CONCLUSION:
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Authors | Robert P Baughman, Marc A Judson, Alvin S Teirstein, David R Moller, Elyse E Lower |
Journal | Chest
(Chest)
Vol. 122
Issue 1
Pg. 227-32
(Jul 2002)
ISSN: 0012-3692 [Print] United States |
PMID | 12114363
(Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Immunosuppressive Agents
- Thalidomide
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Topics |
- Adult
- Chronic Disease
- Dose-Response Relationship, Drug
- Female
- Humans
- Immunosuppressive Agents
(adverse effects, therapeutic use)
- Male
- Middle Aged
- Photography
- Sarcoidosis
(drug therapy, pathology)
- Skin Diseases
(drug therapy, pathology)
- Thalidomide
(adverse effects, therapeutic use)
- Treatment Outcome
- United States
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