Literature DB >> 16764332

[Arrhythmogenic right ventricular cardiomyopathy with pulmonary embolism: a case report].

Takayoshi Hirota1, Hiroaki Kitaoka, Toru Kubo, Makoto Okawa, Yosuke Jinnouchi, Takashi Furuno, Yoshinori Doi.   

Abstract

A 50-year-old man complained of dyspnea on exertion. Electrocardiography showed frequent premature ventricular contraction and inverted T wave in leads V1-V6. Echocardiography and right ventriculography showed dilation and systolic dysfunction of the right ventricle. The diagnosis was arrhythmogenic right ventricular cardiomyopathy. In addition, thrombus was also observed in the pulmonary artery on chest computed tomography and pulmonary artery angiography. The final diagnosis was arrhythmogenic right ventricular cardiomyopathy complicated by pulmonary embolism. Pulmonary embolism should be considered in patients with arrhythmogenic right ventricular cardiomyopathy with dyspnea.

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Year:  2006        PMID: 16764332

Source DB:  PubMed          Journal:  J Cardiol        ISSN: 0914-5087            Impact factor:   3.159


  1 in total

1.  Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality.

Authors:  Jia Chen; Yuting Ma; Hong Li; Zhuo Lin; Zhe Yang; Qin Zhang; Feng Wang; Yanping Lin; Zebing Ye; Yubi Lin
Journal:  Orphanet J Rare Dis       Date:  2022-05-07       Impact factor: 4.123

  1 in total

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