Nakamura M, Tachibana H, Mukaeyama T
Department of Surgery, Kakogawa National Hospital, Hyogo, Japan.
Nihon Kyobu Geka Gakkai Zasshi. 1996 Nov;44(11):2082-6.
Leiomyoma of the mediastinum is rare and only 10 cases have been reported in Japan. A 57-year-old woman was admitted to our hospital complaining of dyspnea. Roentgenogram, CT scan and MRI of the chest showed a large mass with well defined margins occupying the posterior mediastinum. With the biopsy neurinoma was suspected and thoracotomy was performed which revealed the mass was not encapsulated and not related to the vagus, esophagus, bronchus, aorta, pulmonary veins. Only the mass was dissected carefully and removed. The operative findings and histology diagnosed it leiomyoma from unknown origin. But we suspected the tumor of originating from the small blood vessels, because they were surrounded with the spindle tumor cells.
纵隔平滑肌瘤很罕见,在日本仅有10例报道。一名57岁女性因呼吸困难入院。胸部X线、CT扫描及MRI显示后纵隔有一边界清晰的巨大肿块。活检怀疑为神经鞘瘤,遂行开胸手术,结果发现肿块无包膜,与迷走神经、食管、支气管、主动脉、肺静脉均无关。仅小心分离并切除肿块。手术所见及组织学检查诊断为来源不明的平滑肌瘤。但我们怀疑肿瘤起源于小血管,因为它们被梭形肿瘤细胞所包绕。