输尿管肉瘤样尿路上皮癌伴软骨肉瘤分化1例。

IF 0.1 4区 医学 Q4 Medicine Analytical and Quantitative Cytopathology and Histopathology Pub Date : 2014-04-01
Marlo M Nicolas, Alia Nazarullah, Charles C Guo
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引用次数: 0

摘要

背景:泌尿道肉瘤样尿路上皮细胞癌预后较差。大多数报告的肉瘤样尿路上皮细胞癌是来自膀胱的病例。少数肿瘤起源于输尿管。病例:我们描述了一个输尿管肉瘤样尿路上皮癌在一个63岁的男子谁接受肾输尿管切除术与膀胱袖。恶性上皮细胞由未分化的多角形细胞和腺状结构组成。上覆粘膜可见尿路上皮原位癌。间充质成分为多形性梭形细胞和腔隙内多核、有丝分裂的非典型软骨细胞。肿瘤扩展到肌层以外的输尿管周围脂肪组织。6个月后肿瘤在腹膜后和骶前区复发。患者接受了化疗和放疗,但在初步诊断后16个月死亡。结论:输尿管肉瘤样尿路上皮癌并不常见。更罕见的是出现恶性异源元素,如软骨肉瘤。这里所描述的病例强调了这些肿瘤的侵袭性。
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Sarcomatoid urothelial carcinoma with chondrosarcomatous differentiation of the ureter: a case report.

Background: Sarcomatoid urothelial cell carcinoma of the urinary tract has a poor prognosis. Most of the reported cases of sarcomatoid urothelial cell carcinomas are those from the urinary bladder. A limited number of these tumors originate from the ureter.

Case: We describe a ureteral sarcomatoid urothelial carcinoma in a 63-year-old man who underwent nephroureterectomy with bladder cuff. The malignant epithelial elements consisted of undifferentiated polygonal cells and areas of glandular formation. Urothelial carcinoma in situ was present in the overlying mucosa. The mesenchymal components were pleomorphic spindle cells and atypical chondrocytes within lacunae with multinucleation and mitoses. The tumor extended beyond the muscularis into the periureteral adipose tissue. The tumor recurred after 6 months in the retroperitoneum and presacral area. The patient received chemotherapy and radiotherapy but died 16 months after the initial diagnosis.

Conclusion: Sarcomatoid urothelial carcinoma of the ureter is uncommon. Even rarer is the presence of malignant heterologous elements such as chondrosarcoma. The case described here underscores the aggressive nature of these neoplasms.

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期刊介绍: AQCH is an Official Periodical of The International Academy of Cytology and the Italian Society of Urologic Pathology.
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