Spider Bites Might Present as Cellulitis Like in Early Cases and Pyoderma Gangrenosum Like in Late Cases

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منابع مشابه

[Pyoderma gangrenosum: a report of 3 cases].

OBJECTIVE To improve the surgeon's understanding of pyoderma gangrenosum (PG) and avoid misdiagnosis and incorrect treatment. METHODS Three cases of PG managed in the department of general surgery during the past 10 years were retrospectively reviewed. RESULTS All of the 3 cases mainly presented with necrosis of skin and soft tissues, followed by formation of painful and extensive creeping ...

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Familial Pyoderma Gangrenosum: About 2 cases

Pyoderma gangrenosum occurrence in a familial pattern is extremely rare. We report pyoderma gangrenosum in two Tunisian siblings with onset respectively at 28 and 26 years old. The initial lesion was a pustule that breaks down to form an ulcer with an erythematous border. Treatment with oral corticosteroids induced an excellent clinical response. This familial clustering suggests a possible gen...

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Pyoderma gangrenosum-like primary cutaneous cryptococcosis.

Sir, The first published case of a Cryptococcus infection was reported by Zenker in 1861 (1), when he described a case of a man dying from a fungal infection involving the central nervous system (CNS). Thereafter, reports of Cryptococcus infections increased significantly. Today most cases occur in immunocompromised, often HIVinfected, individuals (2). C. neoformans (CN) is a ubiquitous yeast-l...

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Sunitinib induced pyoderma gangrenosum-like ulcerations

Pyoderma gangrenosum is a non-infectious neutro?philic skin disease commonly associated with underlying systemic diseases. Histopathological and laboratory diagnostics are unspecific in the majority of the cases and the diagnosis is made in accordance with the clinical picture. Here, we report the case of a 69-year old man with progredient pyoderma gangrenosum-like ulcerations under treatment w...

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[Pyoderma gangrenosum: report of three cases in plastic surgery].

Pyoderma Gangrenosum is a rare disease whose etiology is probably autoimmune. We report two males aged 48 and 49 years and one female aged 54 years, with lesions in the right thigh, right leg and in the borders of a surgical incision in the chest. This article gives a brief description of the lesions, tips for diagnosis and help for the initial management and treatment.

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ژورنال

عنوان ژورنال: Journal of the Turkish Academy of Dermatology

سال: 2020

ISSN: 1307-394X

DOI: 10.4274/jtad.galenos.2020.80299