Yamane T, Kirimoto K, Fujita M, Enomoto Y, Toda T, Kobayashi S, Hada Y, Fukuyama K, Hirata K, Oda T
Dept. of Pathology, Kure National Hospital.
Gan No Rinsho. 1988 Jul;34(8):1036-40.
A case of a leiomyosarcoma of the duodenum is reported. A 52-year-old man with a duodenal submucosal tumor underwent a pancreatico-duodenectomy. Histologically, the resected tumor revealed moderate cellular atypism and moderate pleomorphism, but revealed no mitotic figures. The histological diagnosis was leiomyoma. Nine years after operation, the tumor showed a recurrence and metastasis in the liver. Thus, the patient underwent a lobectomy of the liver. The resected liver tumor showed similar histological features seen in the primary duodenal tumor but with high mitotic activity. Histologically, the patient was diagnosed as having a metastatic leiomyosarcoma. This history suggests that a smooth muscle tumor of potential malignancy, as seen in this case, should be followed continuously, even though mitoses may not be recognized.
报告了一例十二指肠平滑肌肉瘤病例。一名患有十二指肠黏膜下肿瘤的52岁男性接受了胰十二指肠切除术。组织学检查显示,切除的肿瘤有中度细胞异型性和中度多形性,但未见有丝分裂象。组织学诊断为平滑肌瘤。术后九年,肿瘤在肝脏出现复发和转移。因此,患者接受了肝叶切除术。切除的肝肿瘤显示出与原发性十二指肠肿瘤相似的组织学特征,但有高有丝分裂活性。组织学上,患者被诊断为转移性平滑肌肉瘤。该病例提示,即使未发现有丝分裂象,对于这种潜在恶性的平滑肌肿瘤也应持续随访。