=Abstract=
A Case of Intrarenal Neuroblastoma
Ai-Ri Han, M.D., Seok-Joo Han, M.D., Jung-Tak Ob, M.D., Seung-Hoon Choi, M.D., Eui-Ho Hwang, M.D.
Division 0/ Pediatric Surgery, Department 0/ Surgery, Yonsei University College 0/ Medicine, Seoul, Korea
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.
Index Words: Neuroblastoma, Wilms' tumor, Kidney, Children
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Correspondence: Seok-Joo Han, M.D., Division of Ped- iatric Surgery, Department of Surgery, Yonsei University College of Medicine, 132 Shinchon-dong, Seodaemoon-ku, Seoul 120-752, Korea
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Fig. 1. Computed tomography findings of the intra renal tumor; showing the intact capsule of the tumor (arrow) and intrarenal hemorrhage (arrow head).
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Fig. 2. Gross appeance of the tumor showing the ureter (arrow) and intact capsule of the tumor.
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Fig. 3. Microscopic fmding of the tumor, showing the Gerota's fascia (arrow) and small round cells (star) in the renal parenchym (H&E, x 200).
Fig. 4. Microscopic finding of the tumor, showing the glomerulus (thin arrow) and small round cells (thick arrow) (H&E, X 400).
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