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酷似肺栓塞的肺动脉肉瘤。

Pulmonary artery sarcoma mimicking a pulmonary embolism.

作者信息

Sandhu A, Yates T J, Kuriakose P

机构信息

Departments of Internal Medicine, Henry Ford Hospital, 2799 West Grand Blvd, Detroit, MI 48202, USA.

出版信息

Indian J Cancer. 2008 Jan-Mar;45(1):27-9. doi: 10.4103/0019-509x.40643.

Abstract

Sarcomas involving the lung are a rare occurrence, often a result of metastatic disease from primary malignancies involving the skin, liver, breast or heart. Primary pulmonary artery sarcomas are rarer still, with limited cases reported world-wide and consequently data regarding treatment modalities are sparse and largely experimental. These tumors are often mistaken for a pulmonary embolism and seemingly supported by radiological findings. Patients will often present without symptom resolution despite therapeutic anticoagulation. The following case illustrates how a soft tissue sarcoma of the pulmonary artery can mimic a pulmonary embolism, thus, resulting in both a diagnostic and therapeutic dilemma. A positron emission tomography scan was an invaluable tool in this case, showing increased radiotracer uptake and placing neoplasm at the top of the differential diagnosis. This ultimately led to a biopsy that was vimentin positive, cytokeratin negative and CD117 negative, thus consistent with soft tissue sarcoma.

摘要

累及肺部的肉瘤较为罕见,通常是皮肤、肝脏、乳腺或心脏原发性恶性肿瘤转移所致。原发性肺动脉肉瘤更为罕见,全球报道的病例有限,因此关于治疗方式的数据稀少且大多处于试验阶段。这些肿瘤常被误诊为肺栓塞,放射学检查结果似乎也支持这一诊断。尽管进行了抗凝治疗,患者的症状往往仍无缓解。以下病例说明了肺动脉软组织肉瘤如何酷似肺栓塞,从而导致诊断和治疗上的两难困境。在此病例中,正电子发射断层扫描是一项极有价值的工具,显示放射性示踪剂摄取增加,使肿瘤在鉴别诊断中位列首位。这最终促使进行了活检,结果显示波形蛋白阳性、细胞角蛋白阴性、CD117阴性,从而确诊为软组织肉瘤。

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