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中毒性表皮坏死松解症中的暴发性紫癜:病例报告与综述

Purpura Fulminans in Toxic Epidermal Necrolysis: Case Report and Review.

作者信息

Jones Elizabeth, Stair-Buchmann Megan, Kotliar Sophia, Haith Linwood

机构信息

From the *Department of Medicine, †Nathan Speare Regional Burn Treatment Center, and ‡Department of Pathology, Crozer Chester Medical Center, Upland, Pennsylvania.

出版信息

J Burn Care Res. 2015 Nov-Dec;36(6):e274-82. doi: 10.1097/BCR.0000000000000195.

Abstract

Purpura fulminans (PF) and toxic epidermal necrolysis (TEN) are rare and life-threatening diseases. TEN is a notorious epidermolytic condition, most cases of which are drug induced. TEN is a more severe variant of epidermal necrolysis than Stevens-Johnson syndrome, as it affects a greater percentage of skin surface area. PF occurs in acute severe infections, deficiencies of protein C and S, and rarely, is idiopathic. PF is a thrombotic disorder of hemorrhagic cutaneous infarction and disseminated intravascular coagulation. While the two diseases are distinct in etiology, their clinical presentations can be strikingly similar. This report illustrates the clinical overlap between PF and TEN and reveals the potential for the diseases to coincide. The case of a patient with biopsy-proven TEN who developed PF was reviewed in detail. The topics of PF and TEN were searched using the MEDLINE database to investigate the relationship between the two diseases. Our case report raises diagnostic suspicion for PF in cases of TEN, particularly in patients with rapid clinical deterioration and failure of conventional management. In addition to the case presented from our institution, a similar case has been reported in which biopsy-proven PF clinically mimicked the epidermolytic condition Stevens-Johnson syndrome. These observations reflect that, although rare, conditions of epidermal necrolysis and PF may coincide more frequently than currently recognized.

摘要

暴发性紫癜(PF)和中毒性表皮坏死松解症(TEN)是罕见的危及生命的疾病。TEN是一种臭名昭著的表皮松解病症,其中大多数病例是药物引起的。与史蒂文斯-约翰逊综合征相比,TEN是表皮坏死松解症更严重的变体,因为它累及的皮肤表面积百分比更大。PF发生于急性重症感染、蛋白C和S缺乏,极少数情况下为特发性。PF是一种出血性皮肤梗死和弥散性血管内凝血的血栓形成性疾病。虽然这两种疾病在病因上截然不同,但其临床表现可能极为相似。本报告阐述了PF和TEN之间的临床重叠,并揭示了这两种疾病同时发生的可能性。详细回顾了一例经活检证实为TEN但并发PF的患者病例。利用MEDLINE数据库检索PF和TEN的相关主题,以研究这两种疾病之间的关系。我们的病例报告提示,在TEN病例中,尤其是临床迅速恶化且常规治疗无效的患者,应怀疑并发PF。除了我们机构报告的病例外,还报道了一例类似病例,经活检证实为PF,其临床表现类似表皮松解病症史蒂文斯-约翰逊综合征。这些观察结果表明,尽管罕见,但表皮坏死松解症和PF同时发生的情况可能比目前所认识的更为常见。

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