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一名血液透析患者出现获得性穿通性皮肤病并伴有复杂性蜂窝织炎及截肢。

Acquired perforating dermatosis with associated complicated cellulitis and amputation in a hemodialysis patient.

作者信息

Domingos Ana, Calças Roberto, Carias Eduarda, Vidinha Joana, Malho Guedes Anabela, Santos Viriato, Agostini Patrick, Mendonça Francisco Ildefonso, Leão Neves Pedro

机构信息

Division of Nephrology, Centro Hospitalar e Universitário do Algarve.

University of Algarve - Department of Biomedical Sciences and Medicine, Faro, Portugal.

出版信息

Clin Nephrol Case Stud. 2021 Mar 11;9:33-38. doi: 10.5414/CNCS110297. eCollection 2021.

Abstract

INTRODUCTION

Cutaneous manifestations related to chronic kidney disease (CKD) are common and associated with high morbidity. Acquired perforating dermatosis (APD) occurs mostly in diabetic or CKD patients, namely those undergoing hemodialysis.

CASE REPORT

A 58-year-old male with type 2 diabetes, with long-term insulin use, several microvascular and macrovascular complications, and on maintenance hemodialysis for 5 years presented with a 1-week history of painful, pruritic, umbilicated papules and some punctiform necrotic lesions on his left forearm, both hands, and both amputation stumps. There was no evidence of infection or vascular alterations, and the patient was not responsive to an initial course of topical corticosteroid. These lesions rapidly evolved to larger, coalescent necrotic injuries, with aggravated pain, intense left-hand skin peeling, and the appearance of similar lesions in the trunk, requiring hospital admission. Calciphylaxis and APD were suspected. Skin biopsy was performed and directed treatment initiated, including intradialytic sodium thiosulfate. Histology findings were compatible with APD and also excluded findings suggestive of vasculitis or calciphylaxis. Soon after, difficult-to-treat cellulitis of the left hand and forearm progressed to critical ischemia and amputation. Microbiology analysis revealed as the causative agent.

DISCUSSION

To our knowledge, there are no previously described cases of APD-related cellulitis. Its treatment can be particularly challenging, as lesions can persist and relapse, and chronic scars can develop. behaves as an opportunistic and difficult-to-treat pathogen, complicating the prognosis.

CONCLUSION

APD can be associated with cellulitis and all of its complications in patients with underlying severe vasculopathy. Awareness of this complication in APD with early referral and aggressive treatment might improve the outcomes and quality of life of such patients.

摘要

引言

与慢性肾脏病(CKD)相关的皮肤表现很常见,且发病率较高。获得性穿通性皮肤病(APD)大多发生于糖尿病患者或CKD患者,即接受血液透析的患者。

病例报告

一名58岁的2型糖尿病男性患者,长期使用胰岛素,有多种微血管和大血管并发症,维持性血液透析5年,其左前臂、双手及双侧截肢残端出现疼痛、瘙痒的脐凹状丘疹及一些点状坏死性皮损,病史1周。无感染或血管改变的证据,患者对初始外用糖皮质激素治疗无反应。这些皮损迅速发展为更大的融合性坏死性损伤,疼痛加剧,左手皮肤剧烈脱皮,躯干出现类似皮损,需住院治疗。怀疑为钙质沉着症和APD。进行了皮肤活检并开始针对性治疗,包括透析期间使用硫代硫酸钠。组织学检查结果与APD相符,也排除了提示血管炎或钙质沉着症的表现。此后不久,左手和前臂难治性蜂窝织炎进展为严重缺血并截肢。微生物学分析显示 为病原体。

讨论

据我们所知,此前尚无APD相关蜂窝织炎的病例报道。其治疗可能特别具有挑战性,因为皮损可能持续存在并复发,还可能形成慢性瘢痕。 作为一种机会性且难治的病原体,使预后复杂化。

结论

在有潜在严重血管病变的患者中,APD可能与蜂窝织炎及其所有并发症相关。认识到APD中的这种并发症并早期转诊及积极治疗可能会改善此类患者的预后和生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbb8/7962469/47c3f49c1a1f/CNCS-9-033-1.jpg

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