Granuloma Faciale Treated Successfully with Colchicine

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منابع مشابه

Granuloma faciale successfully treated with topical tacrolimus: a case report.

Granuloma eosinophilicum faciale (GF) is a rare chronic inflammatory disorder of unknown etiology. Although the condition is benign, its treatment is often unsatisfactory. We describe a case of a 60-year-old man with GF resistant to therapy with topical corticosteroids and liquid nitrogen. After 4 months of treatment with topical tacrolimus the lesions resolved, with remission lasting for 2 years.

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Granuloma faciale effectively treated with topical pimecrolimus.

Granuloma faciale (GF) is a rare skin disorder with a chronic-relapsing course. Cutaneous lesions affect predominantly the face of middle-aged Caucasian men with characteristic reddish papules, nodules, or plaques; however, various atypical cases with unusual morphology or extra facial involvement have been reported (1-3). Despite many treatment options, both surgical and medical, GF remains th...

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A case of granuloma faciale successfully treated with oral prednisone, tranilast and thalidomide

Address for correspondence: Xu Chen, Heng Gu, Institute of Dermatology, Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs, Chinese Academy of Medical Science and Peking Union Medical College, 12 Jiangwangmiao St, 210042 Nanjing, China, phone: +86 25 8547 8919, fax: +86 25 85414477, e-mail: [email protected], [email protected] Received: 10.10.2016, accepted: 3.0...

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Wells' Syndrome Successfully Treated with Colchicine

Eosinophilic cellulitis is an uncommon, inflammatory and chronic disorder of unknown etiology. Corticosteroids are currently considered as the first-line treatment but they are not without significant disadvantages such as contraindications in steroid-resistant cases and patients with frequent recurrences. We report a patient suffering from Wells' syndrome with a 24-year history of symptomatic ...

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Granuloma faciale with disseminated extra facial lesions.

Granuloma faciale (GF) is a rare cutaneous disorder categorized as a localized form of small vessel vasculitis. Clinically, it manifests as single or multiple, well-demarcated, red-brown plaques, papules and nodules, nearly always confined to the face. Herein, we report a 39-year-old man with multiple red-brown, infiltrated plaques on his face and extrafacial lesions on the back, shoulders, and...

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ژورنال

عنوان ژورنال: Acta Dermato Venereologica

سال: 2019

ISSN: 0001-5555

DOI: 10.2340/00015555-3209