Park Hee Jin, Jung Seung Min, Song Jason Jungsik, Park Yong Beom, Song Ji Sun, Lee Sang Won
Division of Rheumatology, Department of Internal Medicine, Catholic Kwandong University College of Medicine, International St. Mary's Hospital, Incheon, Korea.
Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Yonsei Med J. 2019 May;60(5):454-460. doi: 10.3349/ymj.2019.60.5.454.
The present study investigated chest computed tomography (CT) patterns and lung histological features, as well as the consistency between radiological and histological features among patients with microscopic polyangiitis (MPA), granulomatosis with polyangiitis (GPA), and eosinophilic GPA (EGPA).
The medical records of 74 antineutrophil cytoplasmic antibody-associated vasculitis (AAV) patients with radiological lung parenchymal lesions were reviewed along with the histological results for 28 of them. Chest CT patterns were divided according 12 items mostly suggested by radiologists and histological features were divided according to necrotising granuloma, necrotising vasculitis, eosinophilic infiltration, and hemosiderin laden macrophages as defined by a pathologist.
The mean age was 57.1 years (22 men). The most common clinical manifestation other than lung manifestation was renal manifestation (62.2%), and the most common chest CT pattern was lung involvement of vasculitis (35.1%). In MPA patients, the major histological features were hemosiderin-laden macrophages in the alveolar space and vasculitis. In GPA patients, the major histological features were necrotizing vasculitis and necrotizing granuloma, while in EGPA patients, the major histological feature was only necrotising vasculitis. The consistency rate in GPA patients was the highest (100%), followed by that in MPA patients (66.7%) and EGPA patients (50.0%).
When lung involvement of AAV is suspected on chest CT, lung biopsy should be recommended for the proper classification of AAV, due to the discordance rate between radiological and histological findings in MPA and EGPA patients, but not GPA patients.
本研究调查了显微镜下多血管炎(MPA)、肉芽肿性多血管炎(GPA)和嗜酸性肉芽肿性多血管炎(EGPA)患者的胸部计算机断层扫描(CT)模式和肺部组织学特征,以及放射学和组织学特征之间的一致性。
回顾了74例抗中性粒细胞胞浆抗体相关性血管炎(AAV)患者的病历,这些患者有放射学上的肺实质病变,其中28例有组织学结果。胸部CT模式根据放射科医生提出的12项内容进行划分,组织学特征根据病理学家定义的坏死性肉芽肿、坏死性血管炎、嗜酸性粒细胞浸润和含铁血黄素巨噬细胞进行划分。
平均年龄为57.1岁(22名男性)。除肺部表现外,最常见的临床表现是肾脏表现(62.2%),最常见的胸部CT模式是血管炎累及肺部(35.1%)。在MPA患者中,主要组织学特征是肺泡腔内含铁血黄素巨噬细胞和血管炎。在GPA患者中,主要组织学特征是坏死性血管炎和坏死性肉芽肿,而在EGPA患者中,主要组织学特征仅是坏死性血管炎。GPA患者的一致性率最高(100%),其次是MPA患者(66.7%)和EGPA患者(50.0%)。
当胸部CT怀疑AAV累及肺部时,由于MPA和EGPA患者放射学和组织学结果的不一致率较高,而GPA患者不一致率较低,因此建议进行肺活检以对AAV进行正确分类。