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多发性骨髓瘤中的白细胞破碎性(小血管)血管炎。

Leukocytoclastic (small vessel) vasculitis in multiple myeloma.

作者信息

Bayer-Garner I B, Smoller B R

机构信息

Department of Pathology, Marshfield Clinic, Marshfield, WI, USA.

出版信息

Clin Exp Dermatol. 2003 Sep;28(5):521-4. doi: 10.1046/j.1365-2230.2003.01324.x.

Abstract

The hallmark of leukocytoclastic vasculitis (LCV) is palpable purpura. Histologically, there is a neutrophilic, angiocentric, segmental inflammation with endothelial cell injury and fibrinoid necrosis of the blood vessel walls. Leukocytoclastic vasculitis has many associations, including, rarely, multiple myeloma (MM). A total of 2357 patients with a diagnosis of MM were reviewed to retrieve cases that had developed leukocytoclastic vasculitis. Eight patients with MM and LCV showed a predominance of immunoglobulin G (IgG) myeloma paralleling the immunoglobulin secretion seen overall. Overexpression of interleukin 6, which is necessary for myeloma cell growth and survival, may contribute to the pathogenesis of LCV in the setting of MM.

摘要

白细胞破碎性血管炎(LCV)的标志是可触及的紫癜。组织学上,存在嗜中性、血管中心性、节段性炎症,伴有内皮细胞损伤和血管壁纤维蛋白样坏死。白细胞破碎性血管炎有许多关联因素,包括罕见的多发性骨髓瘤(MM)。对总共2357例诊断为MM的患者进行了回顾,以检索发生白细胞破碎性血管炎的病例。8例MM合并LCV患者显示免疫球蛋白G(IgG)骨髓瘤占优势,这与总体上观察到的免疫球蛋白分泌情况相似。白细胞介素6的过表达对骨髓瘤细胞的生长和存活至关重要,可能在MM背景下促成LCV的发病机制。

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