A Case of Intrarenal Neuroblastoma

신장에서 발생한 신경모세포종 1예

  • Han, Ai-Ri (Division of Pediatric Surgery, Department of Surgery, Yonsei University College of Medicine) ;
  • Han, Seok-Joo (Division of Pediatric Surgery, Department of Surgery, Yonsei University College of Medicine) ;
  • Oh, Jung-Tak (Division of Pediatric Surgery, Department of Surgery, Yonsei University College of Medicine) ;
  • Choi, Seung-Hoon (Division of Pediatric Surgery, Department of Surgery, Yonsei University College of Medicine) ;
  • Hwang, Eui-Ho (Division of Pediatric Surgery, Department of Surgery, Yonsei University College of Medicine)
  • 한애리 (연세대학교 의과대학 외과학교실 소아외과) ;
  • 한석주 (연세대학교 의과대학 외과학교실 소아외과) ;
  • 오정탁 (연세대학교 의과대학 외과학교실 소아외과) ;
  • 최승훈 (연세대학교 의과대학 외과학교실 소아외과) ;
  • 황의호 (연세대학교 의과대학 외과학교실 소아외과)
  • Published : 2000.12.30

Abstract

Neuroblastoma arises from the embryonic tissue of the adrenergic rest. It is commonly found in children and mostly in nonrenal tissue. We present a case of intrarenal neuroblastoma which was initially thought to be a Wilms' tumor. The patient was a 18 months-old girl treated with radical nephrectomy and adjuvant chemotherapy after operation. The neoplasm within the kidney in children cannot always indicate Wilms' tumor. Neuroblastoma of the adrenal gland or retroperitoneal tissue may often compress or invade the kidney directly or arise from the kidney. Clinical aspects that differentiate between neuroblastoma and Wilms' tumor are discussed with a review of the literatures.

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