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논문 기본 정보

자료유형
학술저널
저자정보
Dat Quoc Ngo (University of Medicine and Pharmacy at Ho Chi Minh City) Si Tri Le (University Medical Center Ho Chi Minh City) Khanh Hoang Phuong Phan (International NeuroSurgery Hospital) Thao Thi Phuong Doan (University of Medicine and Pharmacy at Ho Chi Minh City) Linh Ngoc Khanh Nguyen (University of Medicine and Pharmacy at Ho Chi Minh City) Minh Hoang Dang (University of Medicine and Pharmacy at Ho Chi Minh City) Thien Thanh Ly (University of Medicine and Pharmacy at Ho Chi Minh City) Thu Dang Anh Phan (University of Medicine and Pharmacy at Ho Chi Minh City)
저널정보
대한병리학회 Journal of Pathology and Translational Medicine Journal of Pathology and Translational Medicine Vol.58 No.4
발행연도
2024.7
수록면
174 - 181 (8page)
DOI
10.4132/jptm.2024.05.02

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Background: The identification of idiopathic inflammatory myopathies (IIMs) requires a comprehensive analysis involving clinical manifestations and histological findings. This study aims to provide insights into the histopathological and immunohistochemical aspects of IIMs. Methods: This retrospective case series involved 56 patients diagnosed with IIMs at the Department of Pathology, University of Medicine and Pharmacy at Ho Chi Minh City, from 2019 to 2023. The histology and immunohistochemical expression of HLA-ABC, HLA-DR, C5b-9, Mx1/2/3, and p62 were detected. Results: We examined six categories of inflammatory myopathy, including immunemediated necrotizing myopathy (58.9%), dermatomyositis (DM; 23.2%), overlap myositis (8.9%), antisynthetase syndrome (5.4%), inclusion body myositis (IBM; 1.8%), and polymyositis (1.8%). The average age of the patients was 49.7 ± 16.1 years, with a female-to-male ratio of 3:1. Inflammatory cell infiltration in the endomysium was present in 62.5% of cases, perifascicular atrophy was found in 17.8%, and fiber necrosis was observed in 42 cases (75.0%). Rimmed vacuoles were present in 100% of cases in the IBM group. Immunohistochemistry showed the following positivity rates: HLA-ABC (89.2%), HLA-DR (19.6%), C5b-9 (57.1%), and Mx1/2/3 (10.7%). Mx1/2/3 expression was high in DM cases. p62 vacuole deposits were noted in the IBM case. The combination of membrane attack complex and major histocompatibility complex I helped detect IIMs in 96% of cases. Conclusions: The diagnosis of IIMs and their subtypes should be based on clinical features and histopathological characteristics. Immunohistochemistry plays a crucial role in the diagnosis and differentiation of these subgroups.

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