肺动脉原发性黏液肉瘤的外科治疗。

J Simek, B Král, F Langr
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引用次数: 0

摘要

病例47岁的男子,临床患有反复呼吸困难,咳嗽,晕厥,咯血,抗凝和纤溶药物治疗不成功,被描述。在手术中切除了一大块肿瘤,几乎占据了整个肺动脉管腔并延伸到周围的分支。肿瘤经组织学和免疫组织化学分类为黏液肉瘤。手术后,患者无症状,在接下来的14个月里可以做他原来的工作(卡车司机)。他在手术后20个月去世,表现出进行性右心衰的症状和体征。尸检时,发现肿瘤闭塞的肺动脉和邻近血栓形成。复发性肺血栓栓塞的鉴别诊断应考虑原发性肺动脉肉瘤,特别是当未发现外周静脉血栓形成时。
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Surgical treatment of pulmonary artery primary myxosarcoma.

Case of the 47-year-old man, clinically suffering from recurrent dyspnoea, cough, syncopes, haemoptysis, unsuccessfully treated with anticoagulant and fibrinolytic agents, is described. Large masses of a tumour, occupying nearly the whole lumen of pulmonary artery and extending to peripheral branches, were removed during surgery. The tumour was histologically and immunohistochemically classified as myxosarcoma. Following surgery, the patient was asymptomatic, could do his original job (lorry-driver) for the next 14 months. He died 20 months after surgery, showing symptoms and signs of progressive right heart failure. At autopsy, the tumourous obliteration of the pulmonary artery and adjacent thrombosis were found. Primary pulmonary artery sarcoma should be considered in the differential diagnosis of recurrent pulmonary thromboembolism, especially when no peripheral vein thrombosis could be found.

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