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1例表现为酷似肺恶性肿瘤的肉芽肿性多血管炎病例。

A case of granulomatosis with polyangiitis mimicking lung malignancy.

作者信息

Han Michael, Pan Corinna

机构信息

Department of Respiratory and Sleep Medicine Sutherland Hospital Sydney New South Wales Australia.

出版信息

Respirol Case Rep. 2021 Aug 9;9(9):e0824. doi: 10.1002/rcr2.824. eCollection 2021 Sep.

Abstract

Patients with granulomatosis with polyangiitis (GPA) may present with varied manifestations including pulmonary masses and nodules. We report the case of a 45-year-old man presenting with cough, haemoptysis and weight loss in the context of a 20 pack-year past smoking history. Computed tomography (CT) of the chest and positron emission tomography/CT scan demonstrated two right upper lobe masses, bilateral lung nodules and mediastinal lymphadenopathy, with increased fluorodeoxyglucose avidity. Endobronchial and CT-guided lung biopsy demonstrated granulomatous inflammation and elevated c-ANCA/PR3 confirmed the diagnosis of GPA. The patient received induction therapy with methylprednisolone and rituximab with good clinical response. Our case highlights the importance of considering a wide range of differentials in patients with lung masses/nodules, including autoimmune pathologies.

摘要

肉芽肿性多血管炎(GPA)患者可能有多种表现,包括肺部肿块和结节。我们报告一例45岁男性病例,该患者有20包年的吸烟史,出现咳嗽、咯血和体重减轻。胸部计算机断层扫描(CT)和正电子发射断层扫描/CT显示右上叶有两个肿块、双侧肺结节和纵隔淋巴结肿大,氟脱氧葡萄糖摄取增加。支气管内及CT引导下肺活检显示肉芽肿性炎症,c-ANCA/PR3升高确诊为GPA。患者接受甲泼尼龙和利妥昔单抗诱导治疗,临床反应良好。我们的病例强调了在有肺部肿块/结节的患者中考虑多种不同鉴别诊断的重要性,包括自身免疫性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9269/8350426/2f85987ab08f/RCR2-9-e0824-g003.jpg

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