SUN-037 Operative Ethanol Ablation as a Treatment for Pediatric Pancreatic Neuroendocrine Tumors

Abstract Disclosure: R. El Mouallem: None. T. McKenzie: None. A.N. Lteif: None. Background- Pancreatic neuroendocrine tumors (PNETs) are rare, but their incidence is rising. Ethanol ablation is increasingly used in adult patients with insulinomas or small nonfunctional PNETs, particularly in patients who are ineligible for surgical resection. Ethanol ablation of a PNET has not been previously reported in the pediatric population. Clinical Case- A 12-year-old female with known multiple endocrine neoplasia type 1 (MEN1) and multifocal PNETs presented for evaluation of a 1.3 cm nonfunctional, Dotatate avid pancreatic uncinate lesion. A CT angiogram of the pancreas revealed an arterially enhancing 1.3 cm nodule, which measured 8 mm one year prior. There was no evidence of metastatic disease. Given the increasing size of the lesion and young age of the patient, operative intervention was pursued. Due to the depth of the lesion and its proximity to the pancreatic duct during operative pancreas ultrasonography, surgical enucleation was deemed non-feasible. During the procedure, 7 additional subcentimeter pancreatic lesions concerning for PNETs were identified in the pancreatic body, tail, head and neck-body junction. Ultrasound guided ethanol ablation of the primary lesion was performed. Follow-up imaging demonstrated a promising response. 7 months post ablation, a Dotatate PET CT scan showed persistent focal uptake in the region of the ablated nodule. However, by 9 months, MRI abdomen revealed a decrease in the size of the lesion, now measuring 6 mm, with stable Dotatate uptake. By 19 months post ethanol ablation, the previously hyper-enhancing lesion was no longer visible on MRI, demonstrating complete structural resolution. Conclusion- This case demonstrates that ethanol ablation is a promising treatment option for PNETs in the pediatric population. Given the complexities of surgical resection in children, particularly for deep or anatomically challenging lesions, ethanol ablation offers a potentially less morbid alternative with encouraging outcomes. Further research may establish this approach as a viable option for select pediatric patients. Presentation: Sunday, July 13, 2025

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Journal
Journal of the Endocrine Society
Published
2025-10-01
DOI
https://doi.org/10.1210/jendso/bvaf149.1626
Primary Topic
Neuroendocrine Tumor Research Advances
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article
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article

SUN-037 Operative Ethanol Ablation as a Treatment for Pediatric Pancreatic Neuroendocrine Tumors

Travis J. McKenzie, Aida Lteif, Rayane El Mouallem
Journal of the Endocrine Society
Neuroendocrine Tumor Research Advances
article

SUN-037 Operative Ethanol Ablation as a Treatment for Pediatric Pancreatic Neuroendocrine Tumors

Travis J. McKenzie, Aida Lteif, Rayane El Mouallem
article en

Abstract

Abstract Disclosure: R. El Mouallem: None. T. McKenzie: None. A.N. Lteif: None. Background- Pancreatic neuroendocrine tumors (PNETs) are rare, but their incidence is rising. Ethanol ablation is increasingly used in adult patients with insulinomas or small nonfunctional PNETs, particularly in patients who are ineligible for surgical resection. Ethanol ablation of a PNET has not been previously reported in the pediatric population. Clinical Case- A 12-year-old female with known multiple endocrine neoplasia type 1 (MEN1) and multifocal PNETs presented for evaluation of a 1.3 cm nonfunctional, Dotatate avid pancreatic uncinate lesion. A CT angiogram of the pancreas revealed an arterially enhancing 1.3 cm nodule, which measured 8 mm one year prior. There was no evidence of metastatic disease. Given the increasing size of the lesion and young age of the patient, operative intervention was pursued. Due to the depth of the lesion and its proximity to the pancreatic duct during operative pancreas ultrasonography, surgical enucleation was deemed non-feasible. During the procedure, 7 additional subcentimeter pancreatic lesions concerning for PNETs were identified in the pancreatic body, tail, head and neck-body junction. Ultrasound guided ethanol ablation of the primary lesion was performed. Follow-up imaging demonstrated a promising response. 7 months post ablation, a Dotatate PET CT scan showed persistent focal uptake in the region of the ablated nodule. However, by 9 months, MRI abdomen revealed a decrease in the size of the lesion, now measuring 6 mm, with stable Dotatate uptake. By 19 months post ethanol ablation, the previously hyper-enhancing lesion was no longer visible on MRI, demonstrating complete structural resolution. Conclusion- This case demonstrates that ethanol ablation is a promising treatment option for PNETs in the pediatric population. Given the complexities of surgical resection in children, particularly for deep or anatomically challenging lesions, ethanol ablation offers a potentially less morbid alternative with encouraging outcomes. Further research may establish this approach as a viable option for select pediatric patients. Presentation: Sunday, July 13, 2025

Journal of the Endocrine SocietyVol. 9(Supplement_1)
Mayo Clinic in Arizona (US)
Openalex Percentile: Top 59%
Neuroendocrine Tumor Research Advances
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