Renal immature teratoma in infant: A rare case report

Renal teratoma is a rare malignant tumour originating from pluripotent cells. A five-month-old female presented with a painless abdominal mass initially suspected to be a Wilms tumor. A CT scan showed a large tumor in the left abdomen, leading to a left open nephrectomy. Histopathology confirmed an...

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Bibliographic Details
Main Authors: Yacobda Hamonangan Sigumonrong, Aze Andrea Putra
Format: Article
Language:English
Published: Elsevier 2025-03-01
Series:Urology Case Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S2214442025000385
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Summary:Renal teratoma is a rare malignant tumour originating from pluripotent cells. A five-month-old female presented with a painless abdominal mass initially suspected to be a Wilms tumor. A CT scan showed a large tumor in the left abdomen, leading to a left open nephrectomy. Histopathology confirmed an immature Grade III teratoma, showing ectodermal, mesodermal, and endodermal components with neuroepithelial structures. Post-operatively, the patient was stable with a good surgical wound. Diagnosis of renal teratoma relies on histology, as pre-operative imaging may mimic other tumors. Surgical removal is the primary treatment, with chemotherapy for recurrence if necessary.
ISSN:2214-4420