Shimizu J, Murakami S, Hayashi Y, Oda M, Morita K, Arano Y, Ishikawa N, Watanabe Y, Nonomura A
Department of Surgery, Kanazawa University School of Medicine.
Jpn J Clin Oncol. 1993 Oct;23(5):313-6.
Primary pulmonary hemangiopericytoma is a very rare tumor. A case of the disease is reported, together with a review of the literature. The patient was a 78-year-old male, who was admitted to hospital with an abnormal shadow on his chest x-ray. A primary tumor, located in the left S4, was resected, and a final diagnosis of hemangiopericytoma of pulmonary origin was made. The disease recurred in the left lower lobe 14 months postoperatively. The patient received radiotherapy and is alive to date, 23 months after the operation.
原发性肺血管外皮细胞瘤是一种非常罕见的肿瘤。本文报告了1例该疾病，并对相关文献进行了综述。患者为78岁男性，因胸部X线检查发现异常阴影入院。位于左肺上叶前段（S4）的原发性肿瘤被切除，最终诊断为肺源性血管外皮细胞瘤。术后14个月，疾病在左肺下叶复发。患者接受了放疗，术后23个月时仍然存活。
