Gukop Philemon, Frassetto Guido, Karapanagiotidis Georgios, Chandrasekaran Venkatachalam
Department of Cardiothoracic Surgery, St George's Hospital, London SW17 0QT, UK.
Case Rep Cardiol. 2012;2012:396319. doi: 10.1155/2012/396319. Epub 2012 Oct 24.
Leiomyosarcoma of the pulmonary vein is rare and has poor prognosis. Its clinical features are nonspecific and mimic benign conditions. Early diagnosis is challenging. Most cases have been diagnosed only at autopsy or on postoperative histology specimens. Treatment is essentially palliative complete surgical excision. We outline the principles of management with the case of a 39-year-old man with leiomyosarcoma of the left pulmonary veins extending into the left atrium. Extensive investigation to achieve early diagnosis and determine extent of disease is essential. Frozen section guided adequate excision of all cardiac tumours and resection of involved lung tissue achieve local disease control. Adjuvant chemoradiotherapy has been shown to enhance survival.
肺静脉平滑肌肉瘤罕见且预后较差。其临床特征不具特异性,类似良性疾病。早期诊断具有挑战性。大多数病例仅在尸检或术后组织学标本上得以确诊。治疗主要是姑息性完全手术切除。我们以一名39岁患有左肺静脉平滑肌肉瘤并延伸至左心房的男性病例为例概述治疗原则。进行广泛检查以实现早期诊断并确定疾病范围至关重要。冰冻切片引导下充分切除所有心脏肿瘤以及切除受累肺组织可实现局部疾病控制。已证明辅助放化疗可提高生存率。