Dermatology Department, Edouard Herriot Hospital, Hospices Civils de Lyon, Claude Bernard Lyon I University, Lyon.
Dermatol Online J. 2021 Mar 15;27(3):13030/qt4qq316vx.
Report _Case Presentation X Photo Vignette _Letter Authors declare that the contents of this article are their own original unpublished findings. Title: Cutaneous calciphylaxis of the glans penis presenting as a gangrenous ulceration Authors: Marie Danset, Cécile Lesort, Denis Jullien, Jean Kanitakis Affiliations: Dermatology Department, Edouard Herriot Hospital, Hospices Civils de Lyon, Claude Bernard Lyon I University, Lyon, France Corresponding Author: Jean Kanitakis, Department of Dermatology, Edouard Herriot Hospital Group, 69437 Lyon Cedex 03, France, Tel: 33-472110301, Email: jean.kanitakis@univ-lyon1.fr Abstract: Calciphylaxis is a rare microvascular disorder causing necrotic skin ulcers. It is characterized by deposits of calcium within vascular walls but its precise pathogenesis remains poorly understood. A major risk factor is end-stage renal disease on dialysis. We report a 67-year-old man with calciphylaxis revealed by an unusual necrotic ulcer of the glans penis. The patient also presented with bilateral panniculitis of the thighs and a calf ulcer. All those lesions were painful, highlighting the value of pain as a diagnostic clue. Penile involvement of calciphylaxis is rare and biopsy is often avoided in this area. However, rapid diagnosis of calciphylaxis is important because early treatment has a better chance of being successful. Our patient's condition deteriorated rapidly with development of bilateral retinal artery occlusion and he died shortly thereafter. This case further highlights the fact that calciphylaxis is a systemic vascular disease with an ominous prognosis.
病例报告 _病例展示 X 照片小插图 _信件 作者声明本文内容为他们自己的原创未发表发现。 标题: 阴茎龟头的皮肤钙化松解症表现为坏疽性溃疡 作者:MarieDanset,CécileLesort,DenisJullien,JeanKanitakis 所属机构:皮肤科,埃多阿尔·赫里奥特医院,里昂民事医院,克劳德·贝尔纳·里昂第一大学,里昂,法国 通讯作者:JeanKanitakis,埃多阿尔·赫里奥特医院集团皮肤科,69437 里昂 Cedex 03,法国,电话:33-472110301,电子邮件:jean.kanitakis@univ-lyon1.fr 摘要: 钙化松解症是一种罕见的微血管疾病,可导致坏死性皮肤溃疡。其特征是血管壁内钙沉积,但确切的发病机制仍知之甚少。一个主要的危险因素是透析的终末期肾病。我们报告了一例 67 岁男性,因阴茎龟头不常见的坏死性溃疡而出现钙化松解症。该患者还伴有双侧大腿脂膜炎和小腿溃疡。所有这些病变都伴有疼痛,这突出了疼痛作为诊断线索的价值。钙化松解症累及阴茎较为罕见,且该区域常避免活检。然而,快速诊断钙化松解症非常重要,因为早期治疗成功的机会更大。我们患者的病情迅速恶化,出现双侧视网膜动脉闭塞,随后不久死亡。该病例进一步强调了钙化松解症是一种预后不良的系统性血管疾病的事实。