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Cutaneous reactions to recombinant human interferon beta-1b: The clinical and histologic spectrum
- Source :
- Journal of the American Academy of Dermatology. 37:553-558
- Publication Year :
- 1997
- Publisher :
- Elsevier BV, 1997.
-
Abstract
- Background: Recombinant human interferon beta-1b has been recently approved for the treatment of multiple sclerosis. A significant proportion of patients treated with this medication experienced cutaneous reactions. Objective: We describe the clinical and histologic features of cutaneous reactions to recombinant human interferon beta-1b. Methods: Consecutive patients with cutaneous reactions to recombinant interferon beta-1b were evaluated clinically and by biopsy. Results: Clinical lesions varied from subtle uninflamed sclerotic dermal plaques to erythematous plaques to cutaneous ulcers at injection sites. The nonsclerotic lesions were frequently painful. The firm plaques showed fibrosis histologically, whereas nonsclerotic inflammatory lesions demonstrated a consistent pattern of vascular thrombosis. Hematologic evaluation demonstrated platelet activation in most patients with inflammatory lesions, a feature also noted before interferon treatment in some patients. Conclusion: Therapy with recombinant interferon beta-1b is associated with a spectrum of cutaneous reactions and vascular thrombosis. (J Am Acad Dermatol 1997;37:553-8.)
- Subjects :
- Pathology
medicine.medical_specialty
Multiple Sclerosis
Platelet Aggregation
Erythema
Biopsy
Pain
Skin Pigmentation
Dermatology
Skin Diseases, Vascular
Adjuvants, Immunologic
Venules
Interferon
Fibrosis
Skin Ulcer
medicine
Humans
Platelet activation
Skin
Sclerosis
medicine.diagnostic_test
business.industry
Multiple sclerosis
Interferon beta-1b
Interferon beta-1a
Thrombosis
Interferon-beta
Platelet Activation
medicine.disease
Recombinant Proteins
medicine.symptom
business
medicine.drug
Subjects
Details
- ISSN :
- 01909622
- Volume :
- 37
- Database :
- OpenAIRE
- Journal :
- Journal of the American Academy of Dermatology
- Accession number :
- edsair.doi.dedup.....216ed4affe916ed4900a4c704b442014