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肺动脉肉瘤:呼吸困难的罕见病因。

Pulmonary artery sarcoma: a rare cause of dyspnoea.

作者信息

Chaachoui Najia, Haik William, Tournoux François

机构信息

Service de Cardiologie, Hôpital Lariboisière, APHP, Paré, Paris, France.

出版信息

Eur J Echocardiogr. 2011 Mar;12(3):E20. doi: 10.1093/ejechocard/jeq174. Epub 2010 Dec 7.

Abstract

A 72-year-old woman with no significant medical history presented to the emergency room for severe dyspnoea. The initial clinical diagnosis was acute pulmonary embolism. Heparin infusion was initiated while awaiting a computed tomographic scan but the patient's condition deteriorated dramatically and stat echocardiogram showed tamponade. Post-evacuation echo showed a dilated right ventricle with pulmonary hypertension and obstruction of the right pulmonary artery by a homogeneous mass attached to the pulmonary artery, suggesting a tumour rather than a thrombus. Computed tomographic scan confirmed the presence of an obstructive mass with almost no perfusion of the right lung. The patient was referred to cardiac surgery and the mass was removed, with anatomo-pathological diagnosis of a typical pulmonary artery sarcoma. Unfortunately, the patient died a few days after surgery. Primary pulmonary artery sarcoma is a rare tumour that arises in the central pulmonary arteries. Clinical presentation is often attributed to other causes of pulmonary hypertension, like pulmonary embolism. Magnetic resonance imaging could help to distinguish a soft tissue mass from a thrombus but definitive diagnosis is almost always made at surgery or autopsy since patients usually present in acute and unstable situations. Prognosis is poor, from several months to a few years, and depends on how early the diagnosis is made, the presence of recurrence or metastasis after surgical resection, and the use of adjuvant therapy like radiation and chemotherapy.

摘要

一名72岁、无重大病史的女性因严重呼吸困难被送往急诊室。初步临床诊断为急性肺栓塞。在等待计算机断层扫描期间开始输注肝素,但患者病情急剧恶化,急诊超声心动图显示心包填塞。心包穿刺引流后的超声心动图显示右心室扩张伴肺动脉高压,右肺动脉被附着于肺动脉的均匀肿块阻塞,提示为肿瘤而非血栓。计算机断层扫描证实存在阻塞性肿块,右肺几乎无灌注。患者被转诊至心脏外科,肿块被切除,解剖病理学诊断为典型的肺动脉肉瘤。不幸的是,患者在手术后几天死亡。原发性肺动脉肉瘤是一种罕见的肿瘤,起源于肺中央动脉。临床表现常归因于其他肺动脉高压病因,如肺栓塞。磁共振成像有助于区分软组织肿块和血栓,但由于患者通常表现为急性和不稳定情况,几乎总是在手术或尸检时才能做出明确诊断。预后很差,从几个月到几年不等,取决于诊断的早晚、手术切除后是否存在复发或转移以及是否使用放疗和化疗等辅助治疗。

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