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Progressive pulmonary stenosis due to huge mediastinal thymoma

机译:由于巨大的纵隔胸腺瘤引起的渐进性肺狭窄

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摘要

A 61-year-old male was presented with shortness of breath, and there was a mediastinal enlargement in the chest radiography. Thorax computed tomography (CT) showed an anterior mediastinal mass with 18×10×12 cm size that pushed the heart and main vascular structures posteriorly (Fig. 1). Positron emission tomography showed an increased fluorodeoxyglucose uptake. Therefore, a biopsy was performed, which proved that thymoma Type B2 is present. Although external mild right pulmonary artery (RPA) compression was observed on CT, transthoracic echocardiography (TTE) did not show a significant gradient. After 9 months, the patient presented with increased dyspnea and chest pain. The admission CT showed increased diameters of thymoma (19×12×15 cm), with severe compression on the left atrium (LA) and RPA (Fig. 2). TTE showed an anteriorly located mass image in the parasternal view that pushed the heart posteriorly (Fig. 3a), LA compression in the apical views (Fig. 3b and 3c), and moderate pulmonary stenosis with 48 mm Hg maximum gradient in the subcostal view, as parasternal short axis view was poor (Fig. 3d). Surgical excision was planned after chemotherapy by the multidisciplinary team.
机译:一名61岁的男性被呼吸急促出现,胸部射线照相中有纵隔扩大。胸部计算断层扫描(CT)显示了前纵隔质量,具有18×10×12cm的尺寸,向后推动心脏和主血管结构(图1)。正电子发射断层扫描显示氟脱氧葡萄糖摄取量增加。因此,进行了活检,其证明存在胸腺型B2。虽然在CT上观察到外部温和右肺动脉(RPA)压缩,但Transthoracic超声心动图(TTE)没有显示出显着的梯度。 9个月后,患者患有呼吸困难和胸痛的增加。入院CT显示胸腺瘤直径增加(19×12×15cm),左心房(LA)和RPA的严重压缩(图2)。 TTE在胸前视图中显示出前方的质量图像,其向后推动心脏(图3A),在顶端视图中的LA压缩(图3B和3C),在亚挡板中具有48毫米HG的中度肺狭窄,正如Parasternal短轴视图差(图3D)。由多学科团队化疗后计划外科切除。

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