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局限型肉芽肿伴多血管炎表现为孤立性肺病变。

Limited granulomatosis with polyangiitis presenting as an isolated lung lesion.

机构信息

Department of Pathology, Mahatma Gandhi Medical College and Research Institute, Sri Balaji Vidyapeeth University, Pillaiyarkuppam, Puducherry, India.

出版信息

Indian J Pathol Microbiol. 2020 Oct-Dec;63(4):611-614. doi: 10.4103/IJPM.IJPM_831_19.

Abstract

Granulomatosis with polyangiitis (GPA) is a systemic necrotizing vasculitis involving small and medium-sized blood vessels and granulomatous inflammation of upper and lower respiratory systems and/or renal system. In the limited form of GPA, there is no systemic involvement of disease with sparing of kidneys. The respiratory system is the commonly involved organ in limited GPA. Herein, we report the case of a 40-year-old male who was initially diagnosed as sarcoidosis clinically. Lung biopsy revealed necrotizing granulomatous angiitis. Diagnosis of GPA was made which was substantiated by antineutrophil cytoplasmic antibody (ANCA) positivity. This was a case of limited GPA with isolated lung involvement. The early diagnosis and initiation of treatment are critical for improved survival of patients with GPA. Tissue biopsy is necessary for the diagnosis of GPA.

摘要

肉芽肿性多血管炎(GPA)是一种系统性坏死性血管炎,累及小动脉和中动脉,并伴有上呼吸道和/或下呼吸道及肾脏系统的肉芽肿性炎症。在 GPA 的局限型中,疾病不累及全身,肾脏不受累。局限型 GPA 中常见的受累器官是呼吸系统。在此,我们报告 1 例 40 岁男性患者,最初临床诊断为结节病。肺部活检显示坏死性肉芽肿性血管炎。抗中性粒细胞胞质抗体(ANCA)阳性,诊断为 GPA。这是一例局限型 GPA,肺部孤立受累。早期诊断和治疗对改善 GPA 患者的生存至关重要。组织活检对于 GPA 的诊断是必要的。

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