双房黏液瘤伴共享柄1例。

Q4 Medicine
Mehrnoush Toufan, Naser Khezerlou-Aghdam, Shahab Masoumi, Mahshid Dehghan, Aisan Akhgari
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引用次数: 0

摘要

黏液瘤是一种罕见的心脏肿瘤,可表现为单个或多个肿瘤。单侧双房黏液瘤的病例报道较少。我们报告一个非常罕见的情况下,这种情况在一个中年妇女,表现为用力呼吸困难和咳嗽。患者静息性心动过速为每分钟105次,心脏听诊发现二尖瓣舒张中期杂音,随后肿瘤肿块集中于尖顶,实验室数据显示c反应蛋白(1+)和肌酸磷酸激酶水平升高。经食道及经胸超声心动图检查显示肿瘤延伸至卵圆孔未闭(PFO)。手术后切除黏液瘤,修复PFO。她出院了,没有进一步的并发症。虽然黏液瘤很少见,但在手术前考虑这种情况是很重要的。通过PFO累及双心房是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Biatrial Myxoma with a Shared Stalk: A Case Report.

Biatrial Myxoma with a Shared Stalk: A Case Report.

Biatrial Myxoma with a Shared Stalk: A Case Report.

Biatrial Myxoma with a Shared Stalk: A Case Report.

Myxomas are rare cardiac neoplasms and may present as single or multiple tumors. Only a few cases of single biatrial myxomas have been reported. We report a very rare case of this condition in a middle-aged woman, presenting with exertional dyspnea and cough. The patient had a resting tachycardia of 105 beats per minute, and cardiac auscultation discovered a mid-diastolic murmur across the mitral valve, followed by a tumor plop focused on the apex and elevated levels of C-reactive protein (1+) and creatine phosphokinase in lab data. The diagnosis was made via transesophageal and transthoracic echocardiographic examinations, showing the tumor extension through a patent foramen ovale (PFO). The operation was undertaken, the myxoma was excised, and the PFO was repaired. She was discharged with no further complications. Although myxomas are rare, considering this condition before surgery is significant. The involvement of both atria via a PFO is possible.

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来源期刊
Journal of Tehran University Heart Center
Journal of Tehran University Heart Center Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.90
自引率
0.00%
发文量
46
审稿时长
12 weeks
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