畸胎样肾母细胞瘤：1例单侧病例报告

Teratoid Wilms' tumor: report of a unilateral case.

作者信息

Vujanić G M

机构信息

Department of Paediatric Pathology, Mother and Child Health Institute, Belgrade, Yugoslavia.

出版信息

Pediatr Pathol. 1991 Mar-Apr;11(2):303-9. doi: 10.3109/15513819109064767.

DOI:10.3109/15513819109064767

PMID:1647006

Abstract

A unilateral teratoid Wilms' tumor was removed 2.5 weeks after the institution of chemotherapy. Teratoid Wilms' tumor is an extremely rare renal tumor, and only four cases, all bilateral, have been reported. Because of the finding of deep cortical intralobar nephroblastomatosis, strongly associated with bilateral Wilms' tumors, the patient has been closely followed since surgery without evidence of tumor in the remaining kidney at 2 years.

摘要

化疗开始2.5周后切除了单侧畸胎样肾母细胞瘤。畸胎样肾母细胞瘤是一种极其罕见的肾肿瘤，仅报告过4例，均为双侧。由于发现深部皮质叶内肾母细胞瘤病与双侧肾母细胞瘤密切相关，该患者自手术后一直密切随访，2年时剩余肾脏未发现肿瘤迹象。