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Main tract stenosis complicated by granulomatous with polyangiitis: A case report

机译:具有多苯炎的肉芽肿症的主要狭窄狭窄:案例报告

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摘要

Granulomatosis with polyangiitis (GPA) is a rheumatic auto-immune disease involved in vasculitis. It is rarely reported that anti-neutrophil cytoplasmic antibodies (ANCAs) associated with GPA would cause main tract stenosis. The current report documents a 54-year-old woman, with a history of severe cough, presented with wheezing and shortness of breath. Although she was treated with cephalosporin antibiotics for half a month, the symptoms were not alleviated. Accordingly, laboratory testing, radiology and pathology was performed at the Department of Respiratory and Critical Care Medicine, Huashan Hospital. Blood samples were tested negative for ANCAs. Chest CT revealed stenosis of the main trachea and uneven thickening of the tracheal wall. Nasal sinuses CT scanning indicated thickening of the nasal mucosa. Pathological analysis demonstrated chronic granulomatous inflammation with focal lesions. According to the classification criteria of ACR/EULAR provisional 2017, the patient was diagnosed with the ANCAs-negative GPA. Following treatment with oral prednisone only for 6 months, obstruction of main tract was significantly improved. This case study is of interest for the promotion a potentially novel therapeutic intervention for GPA associated with the absence ANCA of in clinic.
机译:肉芽肿病变(GPA)是一种涉及血管炎的风湿性自我免疫疾病。很少报道,与GPA相关的抗嗜中性粒细胞细胞质抗体(ANCAS)将导致主要的道狭窄。目前的报告文件文件是一名54岁的女性,具有严重咳嗽的历史,呈现出喘息和呼吸急促。虽然她被头孢菌素抗生素治疗了半个月,但症状并不缓解。因此,在华山医院呼吸系统和批判性医学系进行了实验室测试,放射学和病理学。血液样品对ANCAS进行阴性。胸部CT揭示了主气管的狭窄,气管墙的增厚不均匀。鼻窦CT扫描表明鼻粘膜的增厚。病理分析表明慢性粒状炎症与焦点病变。根据2017年ACR /欧洲临时临时的分类标准,患者被诊断为ACAS阴性GPA。在用口服泼尼松治疗后6个月后,妨碍主干道显着提高。这种情况研究对促进临床缺失的GPA潜在的新疗效干预感兴趣。

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