A rare large vessels involvement in a patient with a clinical diagnosis of Granulomatosis with polyangiitis: A case report.

IF 0.9 Q4 RHEUMATOLOGY
Mona Terkmani, Yasmin Najjar, Fatema Naddaf, Sana Shaikh Torab, Taher Sawas, Sami Albitar
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引用次数: 0

Abstract

A previously healthy 22-year-old female presented with complaints of fatigue, joints pain, headache, fever and night sweats for several months. She also reported a reddish painful left eye and a rash on her legs two months ago. On examination, her blood pressure was elevated at 160/100 mm/hg and her lower limb pulses were hardly palpable. On investigation, she had anterior and intermediate uveitis, nasal septal ulcer, proteinuria, positive C-ANCA and a computed tomography angiography showed multiple abdominal aortic aneurysms and occlusion of both the left common carotid artery and the right superficial femoral artery. Lymph node biopsy showed necrotizing granulomatous inflammation. The patient was diagnosed with granulomatosis with polyangiitis with large vessels involvement which is a rare finding.

临床诊断为肉芽肿病合并多血管炎的罕见大血管受累1例。
既往健康的22岁女性,主诉疲劳、关节痛、头痛、发热和盗汗数月。她还报告说两个月前左眼发红疼痛,腿上有皮疹。检查时,她的血压升高到160/100 mm/hg,下肢脉搏几乎摸不到。经检查,她有前、中葡萄膜炎,鼻中隔溃疡,蛋白尿,C-ANCA阳性,计算机断层血管造影显示多发腹主动脉瘤,左侧颈总动脉和右侧股浅动脉闭塞。淋巴结活检显示坏死性肉芽肿性炎症。患者被诊断为肉芽肿病合并多血管炎,并累及大血管,这是一种罕见的发现。
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CiteScore
1.40
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