The interaction of inflammatory cells in granuloma faciale

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The interaction of inflammatory cells in granuloma faciale

Granuloma faciale (GF) is a rare chronic inflammatory skin disease characterized by single or multiple reddish-brown cutaneous plaques or nodules. Although this condition is benign, its clinical course is extremely chronic with poor response to therapy. The typical histopathological features of GF include vasculitis with mixed cellular infiltration; however, its etiopathogenesis remains unknown...

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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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An unusual presentation of granuloma faciale

Granuloma faciale (GF) is a benign disease that presents as solitary or multiple asymptomatic plaques on the face. We report a 25-year-old male patient with asymptomatic papular, pustular, and nodular lesions on both cheeks. Diagnosis of GF was made based on the histopathological findings. He was treated with cryotherapy and intralesional triamcinolone injections every month. After 3 months, th...

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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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Granuloma faciale mimicking rhinophyma: response to clofazimine.

Sir, Granuloma faciale (GF) is a rare, but distinct in ̄ammatory dermatosis of unknown origin diagnosed on a combination of clinical and histopathological ®ndings. The clinical presentation may be very variable and can simulate a great variety of dermatosis. The treatment is not well established and in many cases may be unsatisfying and frustrating. We report here a case of disabling and dis®gur...

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ژورنال

عنوان ژورنال: Dermatology Reports

سال: 2010

ISSN: 2036-7406,2036-7392

DOI: 10.4081/dr.2010.e17