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Echocardiographic Assessment in Patients with Granulomatosis with Polyangiitis.

作者信息

Życińska Katarzyna, Borowiec Anna, Zielonka Tadeusz M, Rusinowicz Tomasz, Hadzik-Błaszczyk Małgorzata, Cieplak Magda, Wardyn Kazimierz A

机构信息

Department of Family Medicine, Internal and Metabolic Diseases, Warsaw Medical University, 1A Banacha Street, 02-097, Warsaw, Poland.

出版信息

Adv Exp Med Biol. 2017;1022:27-33. doi: 10.1007/5584_2017_43.

DOI:10.1007/5584_2017_43
PMID:28573446
Abstract

Granulomatosis with polyangiitis (GPA) is one of the most common forms of systemic vasculitis, which usually involves the upper and lower respiratory tract, but it may affect also multiple organs. The aim of the study was an echocardiographic evaluation of cardiac involvement in GPA patients during remission. Eighty eight patients with GPA were evaluated in the study. The control group consisted of 40 age and sex-matched patients without a previous history of cardiovascular disease. We found that there were no differences between GPA and control groups regarding left atrial enlargement and interventricular septal hypertrophy. In one GPA patient, all heart chambers were enlarged. Left ventricle systolic function was decreased (LVEF ≤ 50%) in eight patients with GPA, and left ventricle wall motion abnormalities were observed in 12 patients. Left ventricle relaxation dysfunction, mitral valve and tricuspid valve regurgitation were observed with the same frequency in both GPA and control groups. Aortic regurgitation was the single abnormality that occurred significantly more often in the GPA group than in controls (28% vs. 7.5%; p = 0.03). Pericardial effusion was observed in three GPA patients and in none from the control group. We conclude that the most common echocardiographic manifestation in GPA patients in remission was aortic valve regurgitation. However, cardiac involvement in such patients is rather rare and in the majority of cases clinically insignificant.

摘要

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引用本文的文献

1
Granulomatosis with polyangiitis: clinical characteristics and updates in diagnosis.肉芽肿性多血管炎:临床特征与诊断进展
Front Med (Lausanne). 2024 Aug 27;11:1369233. doi: 10.3389/fmed.2024.1369233. eCollection 2024.
2
Skin, Heart, and CNS Involvement in Granulomatosis With Polyangiitis: A Case Report.皮肤、心脏和中枢神经系统受累的显微镜下多血管炎:一例报告
Cureus. 2024 Aug 1;16(8):e65935. doi: 10.7759/cureus.65935. eCollection 2024 Aug.
3
Granulomatosis With Polyangiitis (Wegener's Granulomatosis) Complicated by Pericarditis: Our Experience of Two Cases and Comparative Review of Literature.
肉芽肿性多血管炎(韦格纳肉芽肿)合并心包炎:我们两例病例的经验及文献比较综述
CASE (Phila). 2021 Jan 26;5(2):126-136. doi: 10.1016/j.case.2020.11.008. eCollection 2021 Apr.
4
Cardiac imaging of a patient with unusual presentation of granulomatosis with polyangiitis: A case report and review of the literature.一位肉芽肿性多血管炎表现异常的患者的心脏影像学表现:病例报告及文献复习。
J Nucl Cardiol. 2021 Apr;28(2):441-455. doi: 10.1007/s12350-019-01809-6. Epub 2019 Jul 26.
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Echocardiogram: The GPS to GPA's Heart (Granulomatosis with Polyangiitis).超声心动图:GPA心脏(显微镜下多血管炎)的GPS
Case Rep Rheumatol. 2019 Jan 16;2019:7609386. doi: 10.1155/2019/7609386. eCollection 2019.