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Superior vena cava syndrome from an invasive thymoma with transcaval invasion to the right atrium

机译:上腔静脉综合征从侵袭性胸腺瘤伴经腔侵袭到右心房

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Invasive thymoma with transcaval extension to the right atrium is a rare cause of superior vena cava syndrome. We present a case on a 74-year-old female presenting with dyspnea on exertion, and facial and upper extremity swelling. Physical examination revealed mild facial swelling, non-pitting edema involving the upper extremities and distention of superficial veins of the anterior chest wall and jugular veins. An echocardiogram showed moderate right atrial dilation with a mobile mass in the atrial cavity prolapsing through the tricuspid valve. Cardiac magnetic resonance imaging revealed a 9.9 × 4.3 cm heterogeneous mass in the anterior mediastinum compressing the superior vena cava and endovenously extending into the right atrium. Tissue biopsy of the mediastinal mass revealed a type B1 thymoma, further staged as a Masaoka IVa invasive thymoma that underwent successful en bloc resection followed by removal of intracaval and right atrial mass.
机译:经腔延长至右心房的浸润性胸腺瘤是上腔静脉综合征的罕见原因。我们介绍了一个案例,该案例是一名74岁女性,因劳累而出现呼吸困难,面部和上肢肿胀。体格检查发现面部轻度肿胀,上肢无麻点水肿,前壁浅静脉和颈静脉扩张。超声心动图显示适度的右心房扩张,并通过三尖瓣瓣膜在房腔中移动。心脏磁共振成像显示前纵隔有9.9×4.3 cm异质性肿块,压迫上腔静脉并经静脉延伸到右心房。纵隔肿块的组织活检显示为B1型胸腺瘤,进一步发展为Masaoka IVa浸润性胸腺瘤,该肿块经历了成功的整块切除,然后切除了腔内和右房肿块。

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