Severe Pulmonary Embolism, Thrombosis of Lower Extremity, Unexpected Mild Renal Disorder in MPO-ANCA Associated Vasculitis: A Case Report.

Zhong-Hua Liao, Jun-Tao Feng, Jia-le Tang, Li-Ying Luo, Xiao-Zhao Li
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Abstract

Myeloperoxidase antineutrophil cytoplasmic antibody (MPO-ANCA) associated vasculitis is an autoimmune disease usually with severe multiple dysfunction syndrome, especially prominent acute renal failure. A 65-year-old woman was admitted with progressive dyspnoea for six months and fever, sputum with blood, pain of the lower extremities and intermittent claudication for two days, indicating multiple organ involvement (respiratory system, blood vessels). The renal involvement was relatively mild, presenting with microscopic haematuria. The chest computed tomography demonstrated multiple pulmonary embolisms. Ultrasound and computed tomography angiography for the lower extremity vessels showed venous and arterial thrombosis. Exclusion of other diseases that can cause multiple organ damage and thrombosis, the positive perinuclear ANCA and MPO-ANCA strongly support the diagnosis of MPO-ANAC-associated vasculitis. The patient's physical condition has been greatly improved by treatment with corticosteroids and anticoagulation.

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MPO-ANCA相关血管炎的严重肺栓塞、下肢血栓形成、意外轻度肾脏疾病1例报告。
髓过氧化物酶抗中性粒细胞胞浆抗体(MPO-ANCA)相关性血管炎是一种自身免疫性疾病,通常伴有严重的多种功能障碍综合征,尤其是急性肾功能衰竭。一名65岁妇女因进行性呼吸困难住院6个月,并伴有发热、带血痰、下肢疼痛和间歇性跛行2天,表明累及多器官(呼吸系统、血管)。肾脏受累相对轻微,显微镜下表现为血尿。胸部计算机断层扫描显示多发肺栓塞。下肢血管超声及计算机断层血管造影显示静脉及动脉血栓形成。排除其他可引起多器官损害和血栓形成的疾病,核周ANCA和MPO-ANCA阳性有力地支持mpo - anac相关血管炎的诊断。经皮质类固醇和抗凝治疗,病人的身体状况有了很大改善。
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