Primary Multiple Cardiac Myxomas in a Patient without the Carney Complex.

Journal of cardiovascular ultrasound Pub Date : 2016-03-01 Epub Date: 2016-03-24 DOI:10.4250/jcu.2016.24.1.71
Shohei Kataoka, Masato Otsuka, Masayuki Goto, Mitsuru Kahata, Asako Kumagai, Koji Inoue, Hiroshi Koganei, Kenji Enta, Yasuhiro Ishii
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引用次数: 4

Abstract

Cardiac tumors are rare, and multiple myxomas are even rarer. The latter phenomenon is mostly associated with the Carney complex, a dominantly inherited disease characterized by multiple primary cardiac myxomas, endocrinopathy, and spotty pigmentation of the skin. We report the rare case of a patient who did not have the Carney complex but had multiple primary cardiac tumors. A 78-year-old woman with a past history of breast cancer was referred to our hospital for further examination of multiple cardiac tumors. Echocardiography showed 4 tumors in the left atrium and left ventricle. We could not diagnose them preoperatively and decided to resect them surgically because they were mobile and could have caused embolism and obstruction. The postoperative pathological findings of all 4 tumors were myxomas, although the patient did not meet the diagnostic criteria of the Carney complex. Therefore, a rare case of multiple primary cardiac myxomas was diagnosed.

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无卡尼复合体患者的原发性多发性心脏黏液瘤。
心脏肿瘤是罕见的,多发性黏液瘤更罕见。后一种现象主要与卡尼复合体有关,卡尼复合体是一种显性遗传性疾病,以多发原发性心脏黏液瘤、内分泌病变和皮肤斑点性色素沉着为特征。我们报告一个罕见的病例,病人谁没有卡尼复杂,但有多个原发性心脏肿瘤。一位78岁的女性,既往有乳腺癌病史,因多发性心脏肿瘤转介至我院接受进一步检查。超声心动图示左心房、左心室肿瘤4例。我们无法在术前诊断出它们,并决定手术切除它们,因为它们是可移动的,可能会导致栓塞和阻塞。4例肿瘤术后病理均为黏液瘤,但患者不符合卡尼复合体的诊断标准。因此,我们诊断了一例罕见的多发性原发心脏黏液瘤。
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