Levy Eli, Korach Amit, Amir Gail, Milgalter Eli
Department of Cardiothoracic Surgery, Hadassah Medical Center, P.O. Box 12000, Jerusalem 91120, Israel.
Heart Lung Circ. 2006 Feb;15(1):62-3. doi: 10.1016/j.hlc.2005.06.009. Epub 2005 Aug 24.
Primary pulmonary artery sarcoma is an uncommon tumor. Mandelstamm in 1923 was the first to describe the disease in an autopsy. Since then, less than 200 cases were reported. The incidence is 0.001-0.03%, they are always highly malignant sarcoma, and women are involved twice as often as men. The presentation is often cough, dyspnea, and chest pain, and patients are usually diagnosed as suffering from pulmonary emboli, and primary tumor of the pulmonary artery is not usually considered in the differential diagnosis. The diagnosis of pulmonary artery sarcoma is made of the "clot" resected during pulmonary artery thrombendarterectomy. Our suggestion is that in patients with unilateral pulmonary artery occlusive disease, no evidence of positive hypercoagulability tests, and no history of thromboembolism, a high suspicion of pulmonary artery sarcoma should be kept in mind, and an angiographic-guided biopsy from the intra-arterial occlusive material should be considered. The treatment is surgery. The survival without operation is less than 2 months. Some patients were treated with adjuvant chemotherapy. We report on a woman with undifferentiated sarcoma of the pulmonary artery, mimicking chronic pulmonary artery emboli. This case illustrates the need to consider malignancy in the differential diagnosis of patients having pulmonary emboli.
原发性肺动脉肉瘤是一种罕见的肿瘤。1923年,曼德尔施塔姆首次在尸检中描述了这种疾病。从那时起,报告的病例不到200例。发病率为0.001%-0.03%,它们均为高度恶性肉瘤,女性患者的发病率是男性的两倍。临床表现通常为咳嗽、呼吸困难和胸痛,患者通常被诊断为患有肺栓塞,在鉴别诊断中通常不会考虑原发性肺动脉肿瘤。肺动脉肉瘤的诊断是通过肺动脉血栓内膜剥脱术中切除的“血栓”做出的。我们的建议是,对于单侧肺动脉闭塞性疾病患者,若没有高凝试验阳性的证据且没有血栓栓塞病史,应高度怀疑肺动脉肉瘤,并考虑对动脉内闭塞物质进行血管造影引导下的活检。治疗方法是手术。未经手术的患者生存期不到2个月。一些患者接受了辅助化疗。我们报告了一名患有肺动脉未分化肉瘤的女性,其症状类似慢性肺动脉栓塞。该病例说明了在对肺栓塞患者进行鉴别诊断时需要考虑恶性肿瘤的可能性。