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Updated: Jun 11, 2025

02:22
Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection
Published on: April 12, 2024
279
Paediatric renal hilar paraganglioma
Ramyasree Bade1, Prema Menon2, Suvradeep Mitra3
1Pediatric surgery, PGIMER, Chandigarh, India.
BMJ Case Reports
|September 30, 2024
Summary
Retroperitoneal paragangliomas are rare, especially in children. This case highlights the successful surgical excision of a renal hilum paraganglioma in a pediatric patient, addressing symptoms like hypertension and abdominal pain.
Area of Science:
- Pediatric Surgery
- Oncology
- Endocrinology
Background:
- Retroperitoneal neuroendocrine tumors are rare, posing surgical challenges, particularly near vital structures like the renal hilum.
- Paragangliomas, a type of neuroendocrine tumor, can occur in the retroperitoneum and present with diverse symptoms.
Observation:
- A pediatric patient presented with abdominal pain, dyspnea, left varicocele, and hypertension.
- Imaging revealed a paraganglioma situated at the renal hilum, adjacent to major renal vessels.
Findings:
- The child underwent successful surgical excision of the retroperitoneal paraganglioma.
- Post-operative recovery was uneventful, with resolution of presenting symptoms.
Implications:
- This case demonstrates the feasibility of complete resection for challenging retroperitoneal paragangliomas in pediatric patients.
- Successful management can alleviate significant symptoms, including hypertension and varicocele, improving quality of life.
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