Infliximab therapy for sarcoidosis (lupus pernio)
Identifieur interne : 001F85 ( Main/Exploration ); précédent : 001F84; suivant : 001F86Infliximab therapy for sarcoidosis (lupus pernio)
Auteurs : H. Haley ; W. Cantrell ; K. Smith [États-Unis]Source :
- British Journal of Dermatology [ 0007-0963 ] ; 2004-01.
English descriptors
- Teeft :
- Activator, Arthritis rheum, Bone cysts, British association, British journal, Clinical disease, Corticosteroid, Cutaneous, Cutaneous disease, Cutaneous lesions, Cyst, Cytokine, Cytotoxic, Cytotoxic therapies, Dermatologist, Dermatology, Disease activity, Etanercept, Granuloma, High dose, High levels, Human murine chimeric antibody, Humoral autoimmunity, Immune, Infliximab, Infusion, Insulin resistance, Internal disease, Ligand, Lupus, Lupus pernio, Metformin hydrochloride, Natural inhibitors, Necrosis, Nodule, Nuclear factor, Oral corticosteroids, Pernio, Rankl, Receptor, Receptor activator, Receptor fusion protein, Rheumatoid, Rheumatoid arthritis, Rheumatoid arthritis patients, Sarcoidosis, Sarcoidosis vasc, Second infusion, Severe disease, Soluble receptor activator, Third infusion, Tumor necrosis factor, Tumour, Tumour necrosis.
Abstract
Sarcoidosis is a chronic granulomatous disease of unknown aetiology in which the primary cytokine tumour necrosis factor (TNF)‐α appears to play a major role. Older immune‐modulating drugs including corticosteroids, antimalarials and thalidomide, as well as cytotoxic drugs with immune modulatory effects, have been used to control disease. We present a patient with severe mutilating cutaneous sarcoidosis (lupus pernio) who had showed only partial response to courses of a wide spectrum of immune modulators and cytotoxic therapies, and who had developed significant side‐effects due to prolonged high‐dose corticosteroids. However, the patient's cutaneous disease responded rapidly to the TNF‐α inhibitor infliximab.
Url:
DOI: 10.1111/j.1365-2133.2004.05769.x
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Sarcoidosis is a chronic granulomatous disease of unknown aetiology in which the primary cytokine tumour necrosis factor (TNF)‐α appears to play a major role. Older immune‐modulating drugs including corticosteroids, antimalarials and thalidomide, as well as cytotoxic drugs with immune modulatory effects, have been used to control disease. We present a patient with severe mutilating cutaneous sarcoidosis (lupus pernio) who had showed only partial response to courses of a wide spectrum of immune modulators and cytotoxic therapies, and who had developed significant side‐effects due to prolonged high‐dose corticosteroids. However, the patient's cutaneous disease responded rapidly to the TNF‐α inhibitor infliximab.</div>
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