Tajima Y, Aizawa M
First Department of Pathology, Hokkaido University School of Medicine, Sapporo, Japan.
Acta Pathol Jpn. 1988 Jun;38(6):805-14. doi: 10.1111/j.1440-1827.1988.tb02352.x.
A case of sarcomatoid carcinoma of the renal pelvis in a 66-year-old male is reported. The patient underwent left nephroureterectomy because of renal pelvic tumor and hydronephrosis. Left renal calcification and atrophy had been diagnosed in the patient about thirty years previously. The tumor showed a polypoid configuration and occupied the renal calyces. Histologically, not only solid nests of transitional cell carcinoma (TCC) and adenocarcinomatous glands but also large spindle-shaped cells with bizarre nuclei simulating sarcoma were identified. Immunoreactive keratin and epithelial-membranous antigen (EMA) were demonstrated in the sarcomatoid cells, indicating that they were of epithelial origin. So far, only 10 cases of so-called sarcomatoid carcinoma or carcinosarcoma of the renal pelvis have been reported in the world. In this report, we summarize the pathological findings of previously reported cases and discuss the histogenesis of this rare tumor.
报告了一例66岁男性肾盂肉瘤样癌病例。患者因肾盂肿瘤和肾积水接受了左肾输尿管切除术。患者约30年前被诊断出左肾钙化和萎缩。肿瘤呈息肉样形态,占据肾盏。组织学上,不仅发现了移行细胞癌(TCC)的实性巢和腺癌性腺管,还发现了具有奇异核的大梭形细胞,类似肉瘤。肉瘤样细胞中显示出免疫反应性角蛋白和上皮膜抗原(EMA),表明它们起源于上皮。迄今为止,世界上仅报道了10例所谓的肾盂肉瘤样癌或癌肉瘤。在本报告中,我们总结了先前报道病例的病理结果,并讨论了这种罕见肿瘤的组织发生。