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文献详情 >Primary Cardiac Lymphoma: Thre... 收藏

Primary Cardiac Lymphoma: Three Case Reports and a Review of the Literature

Primary Cardiac Lymphoma: Three Case Reports and a Review of the Literature

作     者:Clifford Michael Csizmar Zohar Sachs Zuzan Cayci Lihong Bu Michael Andrew Linden Clifford Michael Csizmar;Zohar Sachs;Zuzan Cayci;Lihong Bu;Michael Andrew Linden

作者机构:School of Medicine University of Minnesota Minneapolis USA Division of Hematology Oncology and Transplantation Department of Medicine University of Minnesota Minneapolis USA Department of Radiology University of Minnesota Minneapolis USA Division of Hematopathology Department of Laboratory Medicine and Pathology University of Minnesota Minneapolis USA 

出 版 物:《Open Journal of Blood Diseases》 (血液病期刊(英文))

年 卷 期:2021年第11卷第4期

页      面:120-132页

学科分类:1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学] 

主  题:Primary Cardiac Lymphoma Diffuse Large B Cell Lymphoma Cardiac Tumors 

摘      要:Primary cardiac lymphoma (PCL) is a rare entity that comprises only 1% - 2% of all cardiac tumors. Due to their scarcity and variable clinical presentation, early diagnosis is challenging. In this series, three cases of PCL from a single institution are described, which highlight the spectrum of presenting features and emphasize common principles. In the first case, a 73-year-old male who presented with dyspnea was found to have a 12.1 cm mass in the right ventricle. Biopsy via cardiac catheterization revealed diffuse large B cell lymphoma (DLBCL). He was treated with chemoimmunotherapy and survived for two months. The second case describes a 55-year-old female who presented with chest pain. Imaging revealed a 3.1 cm right atrial mass and bilateral pleural effusions, with cytology from the latter demonstrating DLBCL. She was lost to follow up after three cycles of chemoimmunotherapy. In the last case, an 80-year-old female presented with weakness. A 4.0 cm mass was discovered in the right atrium and the patient expired shortly after admission. Autopsy confirmed the diagnosis of DLBCL. These case summaries are followed by a review of the clinical presentation, diagnostic approach, and treatment outcomes of PCL.

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