Parish J M, Rosenow E C, Swensen S J, Crotty T B
Division of Thoracic Disease and Critical Care Medicine, Mayo Clinic Scottsdale, Ariz, USA.
Chest. 1996 Dec;110(6):1480-8. doi: 10.1378/chest.110.6.1480.
To define characteristic clinical and radiographic presentations of patients found to have primary sarcoma of the pulmonary artery and differentiate this entity from acute and chronic pulmonary thromboembolism. To review pathologic characteristics of pulmonary artery sarcoma.
A retrospective review of medical records at a large medical center and a review of the literature.
Tertiary care medical center.
Patients found to have pulmonary artery sarcoma based on surgical or autopsy findings.
Review of medical records.
Presenting symptoms of patients with pulmonary artery sarcoma are similar to those of patients with other pulmonary vascular disease, including progressive dyspnea, cough, hemoptysis, and chest pain. Symptoms not commonly associated with pulmonary vascular disease consist of progressive weight loss, anemia, and fever, which are symptoms commonly associated with malignancy. The diagnosis is often not suspected prior to surgery, which is often undertaken with an alternative diagnosis such as bronchogenic carcinoma or chronic pulmonary thromboembolism. Prolonged survival is rare; most patients survive only a few months. Survival longer than 3.5 years was not observed. Recent experience with MRI of the thorax and transesophageal echocardiography suggests that these diagnostic entities may be rewarding in separating the abnormalities seen on chest radiographs and angiography from thrombus in the pulmonary artery, mediastinal adenopathy, or primary bronchogenic carcinoma.
Although a rare entity, the key is to suspect the presence of pulmonary artery sarcoma in evaluation of patients with atypical presentations of pulmonary vascular disease especially if associated with symptoms such as weight loss, fever, or anemia.
明确被诊断为原发性肺动脉肉瘤患者的特征性临床和影像学表现,并将该疾病与急慢性肺血栓栓塞症相鉴别。回顾肺动脉肉瘤的病理特征。
对一家大型医疗中心的病历进行回顾性分析,并复习相关文献。
三级医疗中心。
根据手术或尸检结果确诊为肺动脉肉瘤的患者。
病历回顾。
肺动脉肉瘤患者的首发症状与其他肺血管疾病患者相似,包括进行性呼吸困难、咳嗽、咯血和胸痛。与肺血管疾病通常无关的症状包括进行性体重减轻、贫血和发热,这些是通常与恶性肿瘤相关的症状。术前通常不会怀疑该病,手术往往是在考虑其他诊断如支气管源性癌或慢性肺血栓栓塞症的情况下进行。长期生存罕见;大多数患者仅存活数月。未观察到生存超过3.5年的情况。近期胸部MRI和经食管超声心动图的经验表明,这些诊断方法在区分胸部X线片和血管造影所见异常与肺动脉血栓、纵隔淋巴结肿大或原发性支气管源性癌方面可能很有价值。
尽管肺动脉肉瘤是一种罕见疾病,但关键在于在评估具有非典型肺血管疾病表现的患者时怀疑肺动脉肉瘤的存在,尤其是伴有体重减轻、发热或贫血等症状时。