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起源于移行细胞的肉瘤样癌,局限于肾盂。

Sarcomatoid carcinoma of transitional cell origin confined to renal pelvis.

作者信息

Thiel David D, Igel Todd C, Wu Kevin J

机构信息

Department of Urology, Mayo Clinic Jacksonville, Florida 32224, USA.

出版信息

Urology. 2006 Mar;67(3):622.e9-11. doi: 10.1016/j.urology.2005.09.026. Epub 2006 Feb 28.

Abstract

Thirteen reported cases of renal pelvic sarcomatoid carcinoma have been documented since 1961, and all patients presented with metastatic disease or advanced renal parenchyma involvement. The mean survival was shorter than 9 months, and adjuvant therapy appeared to offer no benefit. We present the case of a 61-year-old man with gross hematuria and a large filling defect on computed tomography excretory urography. Surgical pathologic examination after laparoscopic nephroureterectomy was consistent with renal pelvis-confined sarcomatoid carcinoma of transitional cell origin. Adjuvant therapy was not given secondary to the organ-confined nature of disease. The patient was without recurrence for more than 1 year.

摘要

自1961年以来,已有13例肾盂肉瘤样癌的报道病例,所有患者均表现为转移性疾病或晚期肾实质受累。平均生存期短于9个月,辅助治疗似乎并无益处。我们报告一例61岁男性患者,表现为肉眼血尿,计算机断层扫描排泄性尿路造影显示有一个大的充盈缺损。腹腔镜肾输尿管切除术后的手术病理检查结果与起源于移行细胞的肾盂局限性肉瘤样癌相符。由于疾病的器官局限性,未给予辅助治疗。该患者1年多来未复发。

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