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贝切特病中的蓝色趾综合征:一例报告。

Blue Toe Syndrome in Behçet's Disease: A Case Report.

机构信息

Department of General and Vascular Surgery, King Abdullah University Hospital (KAUH), Jordan University of Science and Technology (JUST), Irbid, Jordan.

Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.

出版信息

Am J Case Rep. 2024 Jun 22;25:e943813. doi: 10.12659/AJCR.943813.

Abstract

BACKGROUND Vascular Behçet's disease (VBD) is a rare but potentially life-threatening subtype of Behçet's disease that is characterized by multisystemic vasculitis. It primarily affects males with ancestry traced back to regions along the ancient Silk Road. Both arteries and veins, regardless of size, may exhibit complications, including aneurysmal degeneration or occlusion. While venous involvement is observed in two-thirds of VBD cases, arterial complications are notably the most severe and lethal. Arterial aneurysmal degeneration is more common than occlusive complications, with larger arteries being predominantly affected in VBD. Data regarding isolated small-vessel arterial occlusive disease in VBD are limited. Given the rarity of this presentation in this patient population, it becomes mandatory to thoroughly evaluate such patients to differentiate small-vessel vasculitis from other similar diseases, such as Raynaud's phenomenon, which has a different etiology and management and generally has a more benign course. Here, we delineate the concept of isolated small-vessel vasculitis as a cause of blue toe syndrome in patients with VBD. CASE REPORT This report describes a distinctive case of vascular Behçet's disease in a 51-year-old man who initially exhibited unilateral blue toe syndrome, which swiftly progressed to dry gangrene of the toes. Despite reports of large-vessel involvement, there is a paucity of data on isolated small-vessel vasculitis-induced digital ischemia in VBD. CONCLUSIONS This atypical case underscores the necessity of clinical discernment in differentiating inflammatory microvascular occlusive disease from vasospastic Raynaud's syndrome, both of which can complicate Behçet's disease.

摘要

背景

血管型贝赫切特病(VBD)是一种罕见但潜在危及生命的贝赫切特病亚型,其特征为多系统血管炎。它主要影响有古丝绸之路上相关地区血统的男性。无论大小,动脉和静脉都可能出现并发症,包括动脉瘤样变性或闭塞。虽然 VBD 病例中有三分之二观察到静脉受累,但动脉并发症明显更为严重和致命。动脉动脉瘤样变性比闭塞性并发症更为常见,VBD 中主要影响较大的动脉。关于 VBD 中孤立性小动脉闭塞性疾病的数据有限。鉴于此类患者中这种表现较为罕见,因此必须彻底评估此类患者,将小血管血管炎与其他类似疾病(如雷诺现象)区分开来,后者具有不同的病因和治疗方法,且通常具有更良性的病程。在此,我们阐述了孤立性小血管炎作为 VBD 患者蓝趾综合征的病因概念。病例报告:本报告描述了一例 51 岁男性血管型贝赫切特病的独特病例,该患者最初表现为单侧蓝趾综合征,随后迅速进展为趾干性坏疽。尽管有大血管受累的报告,但关于 VBD 中孤立性小血管炎引起的手指缺血的数据很少。结论:这种非典型病例强调了在区分炎症性微血管闭塞性疾病与血管痉挛性雷诺综合征方面进行临床辨别是必要的,这两种疾病均可使贝赫切特病复杂化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f769/11334092/41f2977a8eed/amjcaserep-25-e943813-g001.jpg

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