A case of granulomatosis with polyangiitis presenting as necrotizing pneumonia: A rare case report

Sonali Mallik, Amanpreet Kaur, Sarada Suna
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Abstract

Systemic vascular diseases frequently involve the respiratory system leading to inflammation of varying-sized vessels in the lungs by various immunological mechanisms. Granulomatosis with polyangiitis (Wegner’s granulomatosis) is one of the rare vascular diseases involving medium and small vessels in various organs. In typical cases, the upper and lower respiratory tract and kidneys are involved producing granulomatous inflammation of small arteries leading to necrotizing vasculitis usually associated with antineutrophil cytoplasmic antibodies (ANCA). Abnormal chest X-rays are seen in almost 70% of the patients during the course of the disease which includes nodules, infiltrate, and necrosis with subsequent cavitation. In rare cases, it may mimic the radiological features of pneumonia thus making the diagnosis difficult. So, here we present a case of a 53-year-old male who presented with necrotizing pneumonia with parapneumonic effusion later found out to be a case of C ANCA positive granulomatosis with polyangiitis.
肉芽肿病合并多血管炎表现为坏死性肺炎:罕见病例报告
全身性血管疾病通常涉及呼吸系统,通过各种免疫机制导致肺部不同大小血管的炎症。多血管性肉芽肿病(Wegner肉芽肿病)是一种少见的累及各脏器中小血管的血管性疾病。在典型病例中,上呼吸道、下呼吸道和肾脏受累,产生小动脉肉芽肿性炎症,导致坏死性血管炎,通常伴有抗中性粒细胞胞浆抗体(ANCA)。近70%的患者在病程中可见异常胸部x线片,包括结节、浸润和坏死并伴有空化。在极少数情况下,它可能模仿肺炎的放射学特征,从而使诊断困难。因此,我们在此报告一个53岁男性的病例,他表现为坏死性肺炎伴肺旁积液,后来发现是一例canca阳性肉芽肿病伴多血管炎。
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