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阴茎坏死作为暴发性紫癜类似福尼尔坏疽的首发体征

Penile Necrosis as a Presenting Sign of Purpura Fulminans Mimicking Fournier's Gangrene.

作者信息

Caputo Valentina, Bonoldi Emanuela, Rongioletti Franco

机构信息

Unit of Surgical Pathology, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy; and.

Unit of Dermatology, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.

出版信息

Am J Dermatopathol. 2021 Jan 1;43(1):e13-e15. doi: 10.1097/DAD.0000000000001744.

Abstract

We report the case of a 63-year-old white man who, 3 days after stent removal of endoscopic drainage of pancreatic cysts, developed a penile necrosis due to purpura fulminans (PF) that has been misdiagnosed as Fournier's gangrene. Penile necrosis was rapidly followed by a lethal multiorgan failure due to disseminated intravascular coagulopathy (DIC), triggered by the subsequent development of a severe acute pancreatitis. PF describes a rare syndrome involving intravascular thrombosis and hemorrhagic infarction of the skin. Although reports of penile necrosis secondary to various causes are documented in the literature, penile necrosis secondary to PF in the setting of acute pancreatitis is a rare event. Histopathologic studies of the skin showing an occlusive nonvasculitic vasculopathy are the first step to achieve an accurate diagnosis.

摘要

我们报告了一例63岁白人男性病例,该患者在胰腺囊肿内镜引流支架取出术后3天,因暴发性紫癜(PF)出现阴茎坏死,最初被误诊为福尼埃坏疽。阴茎坏死后迅速出现致命性多器官功能衰竭,这是由随后发生的严重急性胰腺炎引发的弥散性血管内凝血(DIC)所致。PF是一种罕见的综合征,涉及血管内血栓形成和皮肤出血性梗死。虽然文献中有各种原因导致阴茎坏死的报道,但急性胰腺炎背景下由PF继发的阴茎坏死是罕见事件。皮肤组织病理学检查显示闭塞性非血管炎性血管病是做出准确诊断的第一步。

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