Halank Michael, Jakob Christiane, Kolditz Martin, Hoeffken Gerd, Kappert Utz, Ehninger Gerhard, Weise Matthias
Medizinische Klinik und Poliklinik I, Universitätsklinikum an der TU Dresden, TU Dresden, Germany.
Onkologie. 2010;33(6):313-6. doi: 10.1159/000313861. Epub 2010 May 11.
Pulmonary artery sarcoma is a rare tumor with a poor prognosis.
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.
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.
肺动脉肉瘤是一种罕见的肿瘤,预后较差。
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。
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。