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原发性心脏淋巴瘤与完全性房室传导阻滞:病例报告及文献复习

Primary cardiac lymphoma and complete atrio-ventricular block: case report and review of the literature.

作者信息

Montiel Virginie, Maziers Nicolas, Dereme Thierry

机构信息

Department of Cardiology, Cliniques Universitaires UCL de Mont Godinne, Yvoir, Belgium.

出版信息

Acta Cardiol. 2007 Feb;62(1):55-8. doi: 10.2143/AC.62.1.2019372.

Abstract

Primary cardiac lymphoma (PCL) is a rare and extremely aggressive malignancy, which can express itself by damaging the cardiac conduction system (complete atrio-ventricular block), the myocardium and the pericardium. Histology confirms the diagnosis. Chances of survival depend on early diagnosis and treatment. We present the case of a female patient admitted for severe deterioration of her general state of health who had a complete atrio-ventricular block caused by a tumour of the atrial septum, a B-cell lymphoma stage I. The diagnosis was suggested by combined PET/CT imaging and confirmed by histology of a cardiac biopsy. Her general clinical condition, including the cardiac parameters, significantly improved following chemotherapy induction.

摘要

原发性心脏淋巴瘤(PCL)是一种罕见且极具侵袭性的恶性肿瘤,可通过损害心脏传导系统(完全性房室传导阻滞)、心肌和心包来表现自身。组织学检查可确诊。生存几率取决于早期诊断和治疗。我们报告一例女性患者,因全身健康状况严重恶化入院,其患有由房间隔肿瘤(I期B细胞淋巴瘤)导致的完全性房室传导阻滞。PET/CT联合成像提示了诊断,并经心脏活检组织学检查得以证实。化疗诱导后,她的总体临床状况,包括心脏参数,有了显著改善。

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