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Polyangiitis overlap syndrome: cutaneous leukocytoclastic vasculitis associated with polyarteritis nodosa.

机译:多血管炎重叠综合征:皮肤白细胞碎裂性血管炎伴结节性多动脉炎。

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摘要

A rare case of polyangiitis overlap syndrome is described. The patient was a 25-year-old man who had palpable purpura on his legs which showed leukocytoclastic vasculitis, and polyarteritis nodosa. Superior mesenteric arteriography showed microaneurysms in jejunal branches with focal segmental necrotizing arteritis of small and medium sized muscular arteries in the jejunum. Deposits of IgA and C3 in the superficial blood vessels of the lesional skin were consistent with the features of Henoch-Schönlein purpura. The patient died about two months after initial admission in spite of cytotoxic agent and steroid administration.
机译:描述了一种罕见的多血管炎重叠综合征。该患者是一名25岁的男子,他的腿上有明显的紫癜,显示出白细胞碎裂性血管炎和结节性多发性动脉炎。肠系膜上动脉造影显示空肠分支微动脉瘤,空肠中小型肌肉动脉局灶性节段性坏死性动脉炎。 IgA和C3在病变皮肤浅表血管中的沉积与Henoch-Schönlein紫癜的特征一致。尽管有细胞毒性剂和类固醇给药,但患者在首次入院后约两个月死亡。

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