[Cor triatriatum sinister,病例报告]。

José Luis Conde Salazar, Aldrix Josué Sisniegas Razón, Franz Soplopuco Palacios
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引用次数: 0

摘要

我们报告一例伴有异常肺静脉引流的心房三房性心悸的成人患者,其表现为心悸、下肢水肿、呼吸困难、矫形呼吸、腹侧通气和腹水。临床表现开始于心房颤动发作,与右心衰再次住院有关,因此要求血管断层扫描和经食管超声检查,这导致了最终的诊断。由于严重的二尖瓣和三尖瓣功能不全,手术入路采用全切除多窗纤维肌隔和双瓣成形术,改善了患者的临床状况。在鉴别诊断起源于左心房的右心衰原因时,考虑这种无氰先天性心脏病的重要性是公认的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[Cor triatriatum sinister, case report].

[Cor triatriatum sinister, case report].

[Cor triatriatum sinister, case report].

[Cor triatriatum sinister, case report].

We report a case of cor triatriatum sinister associated with anomalous pulmonary venous drainage in an adult patient who presented with palpitations, lower limb edema, dyspnea, orthopnea, bendopnea and ascites. The clinical picture began with episodes of atrial fibrillation, associated with rehospitalizations for right heart failure, so angiotomography and transesophageal echography were requested, which led to the final diagnosis. The surgical approach was performed by total excision of the multifenestrating fibromuscular septum and double valvular plasty, due to severe mitral and tricuspid insufficiency, which improved the patient's clinical condition. The importance of considering this acyanotic congenital heart disease within the differential diagnosis of the causes of right heart failure originating in the left atrium is recognized.

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CiteScore
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