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表现为严重呼吸困难和右心功能不全的内膜肺动脉肉瘤。

Intimal pulmonary artery sarcoma presenting as severe dyspnea and right heart insufficiency.

作者信息

Halank Michael, Jakob Christiane, Kolditz Martin, Hoeffken Gerd, Kappert Utz, Ehninger Gerhard, Weise Matthias

机构信息

Medizinische Klinik und Poliklinik I, Universitätsklinikum an der TU Dresden, TU Dresden, Germany.

出版信息

Onkologie. 2010;33(6):313-6. doi: 10.1159/000313861. Epub 2010 May 11.

Abstract

BACKGROUND

Pulmonary artery sarcoma is a rare tumor with a poor prognosis.

CASE REPORT

We report the case of a 64-year-old man with an intimal pulmonary artery sarcoma presenting with severe high oxygen flow-demanding dyspnea and weight loss of 12 kg in the last 6 months. On echocardiography, right heart insufficiency, markedly elevated right ventricular pressure, a pressure gradient along the right outflow tract, and a tumor mass adherent to the wall of the truncus pulmonalis were detected. The tentative diagnosis by echocardiographic findings was pulmonary artery sarcoma. Computed tomography of the thorax and 18-fluorodeoxyglucose positron emission tomography showed an advanced local tumor manifestation. Surgical resection of the tumor to improve hemodynamics confirmed the diagnosis.

CONCLUSIONS

Pulmonary artery sarcoma should be considered as a rare differential diagnosis in patients with dyspnea due to right heart failure, particular in the case of additional weight loss, and echocardiographic examination is a useful first diagnostic approach in establishing the diagnosis.

摘要

背景

肺动脉肉瘤是一种罕见的肿瘤,预后较差。

病例报告

我们报告一例64岁男性,患有内膜肺动脉肉瘤,表现为严重的高氧流量需求性呼吸困难,且在过去6个月体重减轻12千克。超声心动图检查发现右心功能不全、右心室压力显著升高、沿右流出道的压力梯度以及附着于肺动脉干壁的肿瘤团块。根据超声心动图检查结果初步诊断为肺动脉肉瘤。胸部计算机断层扫描和18氟脱氧葡萄糖正电子发射断层扫描显示局部肿瘤进展。为改善血流动力学对肿瘤进行手术切除,从而确诊。

结论

对于因右心衰竭导致呼吸困难的患者,尤其是伴有体重减轻的情况,应将肺动脉肉瘤视为一种罕见的鉴别诊断,超声心动图检查是确立诊断的一种有用的初步诊断方法。

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