Hepatoblastoma: a single institutional experience of 18 cases

Parul J Shukla1, Savio G Barreto, Sajid S Qureshi

  • 1Department of Gastrointestinal Surgical Oncology, Tata Memorial Hospital, Parel, Mumbai 400 012, India. pjshukla@doctors.org.uk

Insights

Multidisciplinary management of hepatoblastoma, a rare childhood liver tumor, involving surgery and chemotherapy, achieved complete resection in all patients with low mortality and morbidity. This approach offers a promising survival rate for pediatric liver cancer.

Area of Science:

  • Pediatric Oncology
  • Surgical Oncology
  • Hepatobiliary Surgery

Background:

  • Hepatoblastoma is the most common pediatric liver tumor, though rare overall.
  • Global data integration is needed for multidisciplinary management outcomes.
  • This study reviews single-institution experience with hepatoblastoma resection.

Purpose of the Study:

  • To retrospectively analyze outcomes of surgically resected hepatoblastomas.
  • To evaluate the efficacy of multidisciplinary management including chemotherapy and surgery.
  • To assess survival rates and complications in pediatric hepatoblastoma patients.

Main Methods:

  • Retrospective analysis of 18 pediatric patients with hepatoblastoma.
  • Patients managed surgically with preoperative chemotherapy between 2000-2007.
  • Evaluation of primary outcomes (survival, morbidity) and secondary outcomes (resection completeness).

Main Results:

  • Complete gross resection (Stages I & II) achieved in 100% of patients.
  • Mortality rate was 0%, with morbidity at 11.2%.
  • 80-month disease-free survival was 67%; chemotherapy aided tumor downstaging.

Conclusions:

  • Major liver resection for hepatoblastoma is feasible with minimal complications.
  • Multidisciplinary care, including chemotherapy and surgery, improves outcomes.
  • This study represents a significant contribution to Indian data on hepatoblastoma surgical management.

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