Pediatric Hematology Oncology Journal (Sep 2024)

A 3-year-old child with multifocal (thoracoabdominal) primary neuroblastoma: A case report and literature review

  • Ayesha Rahmat,
  • Swaminathan Keerthivasagam,
  • Sajid Qureshi,
  • Puja Bathala,
  • Mukta Ramadwar,
  • Gramani Arumugam Vasugi,
  • Harshavardhan Mahalingam,
  • Vasundhara Patil,
  • Dhaarani Jayaraman,
  • Julius Xavier Scott

Journal volume & issue
Vol. 9, no. 3
pp. 151 – 154

Abstract

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Introduction: Multifocal primary neuroblastoma in the non-infantile age group is rare, posing challenges in risk stratification and surgery. Case report: A 3-year-old girl presented with an abdominal mass and elevated urinary vanillylmandelic acid (218 mg/l). Positron emission tomography - computed tomography showed fluorodeoxyglucose-avid masses in the left suprarenal and posterior mediastinum with regional paraortic nodes. A biopsy of the suprarenal and thoracic masses was suggestive of ganglioneuroblastoma and ganglioneuroma. She was stratified as an intermediate risk, with the bone marrow being uninvolved and non-amplified MYCN. Gross tumor resection was achieved at all the sites after 2 cycles of neoadjuvant chemotherapy. She received 2 more cycles of adjuvant chemotherapy and has been disease-free for 3 years. Conclusion: Multifocal primaries in the non-infantile age group have favorable biological features and a good outcome.

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