Case Report: Primary Cardiac T-Cell Lymphoma With Complete Atrio-Ventricular Block Diagnosed by Endomyocardial Biopsy

Primary cardiac lymphoma (PCL) is a rare disease, the definite diagnosis of which is sometimes difficult and mainly relies on endomyocardial biopsy. Primary cardiac T-cell lymphoma (PCTL) is an extremely rare sub-type of PCL. Here, we report on a 47-year-old female with PCTL who presented with fever...

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Main Authors: Panpan Chen, Yuanyuan Hao, Xi Qiu, Xibin Xiao, Wei Zhu, Yang Xu, Wenbin Qian
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-06-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.890059/full
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author Panpan Chen
Panpan Chen
Yuanyuan Hao
Yuanyuan Hao
Xi Qiu
Xi Qiu
Xibin Xiao
Xibin Xiao
Wei Zhu
Wei Zhu
Yang Xu
Yang Xu
Wenbin Qian
Wenbin Qian
author_facet Panpan Chen
Panpan Chen
Yuanyuan Hao
Yuanyuan Hao
Xi Qiu
Xi Qiu
Xibin Xiao
Xibin Xiao
Wei Zhu
Wei Zhu
Yang Xu
Yang Xu
Wenbin Qian
Wenbin Qian
author_sort Panpan Chen
collection DOAJ
description Primary cardiac lymphoma (PCL) is a rare disease, the definite diagnosis of which is sometimes difficult and mainly relies on endomyocardial biopsy. Primary cardiac T-cell lymphoma (PCTL) is an extremely rare sub-type of PCL. Here, we report on a 47-year-old female with PCTL who presented with fever, syncope, palpitations, and a third-degree atrioventricular block (AVB) on electrocardiogram. Chemotherapy was administered with two courses of methotrexate, cyclophosphamide, liposomal doxorubicin, vincristine, and dexamethasone (MTX-CHOP). As the tumor vanished, AVB changed from third degree to second degree and finally to sinus rhythm. In conclusion, endomyocardial biopsy is valuable in the diagnosis of primary cardiac lymphoma. It is worth noting that alterations in the electrocardiogram may indicate an attack on the heart by PCTL.
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spelling doaj.art-c9d47e027a4a4cbc81db06cf4e4a16a42022-12-22T00:34:20ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-06-011310.3389/fimmu.2022.890059890059Case Report: Primary Cardiac T-Cell Lymphoma With Complete Atrio-Ventricular Block Diagnosed by Endomyocardial BiopsyPanpan Chen0Panpan Chen1Yuanyuan Hao2Yuanyuan Hao3Xi Qiu4Xi Qiu5Xibin Xiao6Xibin Xiao7Wei Zhu8Wei Zhu9Yang Xu10Yang Xu11Wenbin Qian12Wenbin Qian13Department of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, ChinaKey Laboratory for Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, ChinaDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, ChinaKey Laboratory for Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, ChinaDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, ChinaKey Laboratory for Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, ChinaDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, ChinaKey Laboratory for Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, ChinaDepartment of Cardiology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, ChinaProvincial Key Laboratory of Cardiovascular Research, Hangzhou, ChinaDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, ChinaKey Laboratory for Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, ChinaDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, ChinaKey Laboratory for Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, ChinaPrimary cardiac lymphoma (PCL) is a rare disease, the definite diagnosis of which is sometimes difficult and mainly relies on endomyocardial biopsy. Primary cardiac T-cell lymphoma (PCTL) is an extremely rare sub-type of PCL. Here, we report on a 47-year-old female with PCTL who presented with fever, syncope, palpitations, and a third-degree atrioventricular block (AVB) on electrocardiogram. Chemotherapy was administered with two courses of methotrexate, cyclophosphamide, liposomal doxorubicin, vincristine, and dexamethasone (MTX-CHOP). As the tumor vanished, AVB changed from third degree to second degree and finally to sinus rhythm. In conclusion, endomyocardial biopsy is valuable in the diagnosis of primary cardiac lymphoma. It is worth noting that alterations in the electrocardiogram may indicate an attack on the heart by PCTL.https://www.frontiersin.org/articles/10.3389/fimmu.2022.890059/fullprimary cardiac lymphomaT-cell lymphomacomplete atrioventricular blockimmunotherapycase report
spellingShingle Panpan Chen
Panpan Chen
Yuanyuan Hao
Yuanyuan Hao
Xi Qiu
Xi Qiu
Xibin Xiao
Xibin Xiao
Wei Zhu
Wei Zhu
Yang Xu
Yang Xu
Wenbin Qian
Wenbin Qian
Case Report: Primary Cardiac T-Cell Lymphoma With Complete Atrio-Ventricular Block Diagnosed by Endomyocardial Biopsy
Frontiers in Immunology
primary cardiac lymphoma
T-cell lymphoma
complete atrioventricular block
immunotherapy
case report
title Case Report: Primary Cardiac T-Cell Lymphoma With Complete Atrio-Ventricular Block Diagnosed by Endomyocardial Biopsy
title_full Case Report: Primary Cardiac T-Cell Lymphoma With Complete Atrio-Ventricular Block Diagnosed by Endomyocardial Biopsy
title_fullStr Case Report: Primary Cardiac T-Cell Lymphoma With Complete Atrio-Ventricular Block Diagnosed by Endomyocardial Biopsy
title_full_unstemmed Case Report: Primary Cardiac T-Cell Lymphoma With Complete Atrio-Ventricular Block Diagnosed by Endomyocardial Biopsy
title_short Case Report: Primary Cardiac T-Cell Lymphoma With Complete Atrio-Ventricular Block Diagnosed by Endomyocardial Biopsy
title_sort case report primary cardiac t cell lymphoma with complete atrio ventricular block diagnosed by endomyocardial biopsy
topic primary cardiac lymphoma
T-cell lymphoma
complete atrioventricular block
immunotherapy
case report
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.890059/full
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