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英夫利昔单抗诱导的伴有肾脏受累的小血管血管炎 1 例罕见病例报告。

A Rare Case of Infliximab-Induced Small Vessel Vasculitis With Renal Involvement.

机构信息

University of Colorado, Aurora, USA.

出版信息

J Investig Med High Impact Case Rep. 2023 Jan-Dec;11:23247096231188247. doi: 10.1177/23247096231188247.

Abstract

There are few cases in the literature demonstrating vasculitis induced by tumor necrosis factor-α. There exist even fewer cases of systemic inflammation involving the skin, nerves, and kidneys. Here, we present a novel case of a 27-year-old man with Crohn disease refractory to multiple medications, most recently treated with infliximab. He presented with a 3-week history of non-blanching palpable petechial rash involving his bilateral extremities and right upper extremity as well as lesions with black eschar around his ankles. He was found to have refractory cutaneous small vessel vasculitis, nephrotic range proteinuria, and small fiber neuropathy. This case describes the evaluation and treatment of systemic small vessel vasculitis in the setting of infliximab therapy.

摘要

文献中很少有肿瘤坏死因子-α引起的血管炎的病例。全身性炎症累及皮肤、神经和肾脏的病例就更少了。在这里,我们报告了一例 27 岁的男性克罗恩病患者,他对多种药物治疗均无效,最近接受了英夫利昔单抗治疗。他出现了 3 周的非凹陷性可触及瘀点性皮疹,累及双侧四肢和右上臂,以及踝关节周围有黑色焦痂的病变。他被发现患有难治性皮肤小血管血管炎、肾病范围蛋白尿和小纤维神经病。本病例描述了英夫利昔单抗治疗时全身性小血管血管炎的评估和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4eb/10416652/da6388e90b19/10.1177_23247096231188247-fig1.jpg

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