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肾恶性破骨细胞样巨细胞瘤

Malignant osteoclast-like giant cell tumor of the kidney.

作者信息

Heller K N, Manyak M J, Tabbara S O, Kerr L A

机构信息

Department of Urology and Pathology, The George Washington University Medical Center, Washington, DC 20037, USA.

出版信息

Urology. 1998 Mar;51(3):495-8. doi: 10.1016/s0090-4295(97)00649-3.

Abstract

Osteoclast-like giant cell tumors are rare mesenchymal tumors that typically present in osseous tissue and are remarkable because of their slow growth. We report the sixth documented case of a malignant osteoclast-like giant-cell tumor primary to the kidney of an 81-year-old man with a 5-month history of hematuria. Postnephrectomy analysis of the tumor, including immunohistochemical stains and electron microscopy, confirmed the diagnosis. Although the patient died of unrelated complications, metastatic disease was suspected.

摘要

破骨细胞样巨细胞瘤是罕见的间充质肿瘤,通常出现在骨组织中,因其生长缓慢而显著。我们报告了第六例有记录的原发性肾恶性破骨细胞样巨细胞瘤,患者为一名81岁男性,有5个月血尿病史。对肿瘤进行肾切除术后分析,包括免疫组织化学染色和电子显微镜检查,确诊了该病例。尽管患者死于无关并发症,但怀疑有转移性疾病。

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