Polyarteritis Nodosa with Concurrent CMV Infection: A Case Report and Brief Literature Review.

Q4 Medicine
Lauren Schild, Matthew Schaffer
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引用次数: 0

Abstract

A previously healthy 36-year-old male presented to the ED with a six-week history of severe migratory abdominal pain, nightly fevers, fatigue, and weight loss. Labs showed elevated LFTs, CRP, D-dimer, and lymphocytosis along with positive serology for cytomegalovirus (IgM, IgG, DNA). Abdominal CT showed a superior mesenteric venous thrombosis, portal mesenteric venous thrombosis, and multiple splenic infarcts. Diagnostic angiography revealed numerous arterial microaneurysms consistent with polyarteritis nodosa. CMV infection is typically self-limited with complete recovery within days to weeks and in exceedingly rare cases has been reported to cause venous thromboses and splenic infarctions. Polyarteritis nodosa is an ANCA-negative necrotizing vasculitis of medium muscular arteries that typically presents with systemic symptoms and can affect any organ but typically spare the lungs.

结节性多动脉炎并发巨细胞病毒感染1例并简要文献复习。
先前健康的36岁男性以6周的严重迁移性腹痛、夜间发热、疲劳和体重减轻史就诊于急诊科。实验室显示LFTs、CRP、d -二聚体升高,淋巴细胞增多,巨细胞病毒(IgM、IgG、DNA)血清学阳性。腹部CT显示肠系膜上静脉血栓形成、门静脉血栓形成及多发脾梗死。诊断性血管造影显示大量动脉微动脉瘤符合结节性多动脉炎。巨细胞病毒感染通常是自限性的,在数天至数周内完全恢复,在极其罕见的病例中,已报道引起静脉血栓形成和脾梗死。结节性多动脉炎是一种anca阴性的中肌动脉坏死性血管炎,典型表现为全身性症状,可累及任何器官,但通常不累及肺。
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CiteScore
0.50
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62
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