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Neoadjuvant Peptide Receptor Radionuclide Therapy in a Rare Case of Pediatric Primary Hepatic Gastrinoma.
Mahato, Sougata; Aggarwal, Piyush; Thunga, Chennakeshava; Sood, Ashwani; Kanojia, Ravi P; Nada, Ritambhra; Lal, Sadhna B.
Afiliación
  • Mahato S; From the Departments of Pediatric Gastroenterology and Hepatology.
  • Aggarwal P; Nuclear Medicine.
  • Thunga C; From the Departments of Pediatric Gastroenterology and Hepatology.
  • Sood A; Nuclear Medicine.
  • Kanojia RP; Pediatric Surgery.
  • Nada R; Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Lal SB; From the Departments of Pediatric Gastroenterology and Hepatology.
Clin Nucl Med ; 49(4): e161-e163, 2024 Apr 01.
Article en En | MEDLINE | ID: mdl-38427960
ABSTRACT
ABSTRACT Gastrinomas with predilection for the adult male population are located in the gastrinoma triangle (>90%). Primary hepatic gastrinoma especially in pediatric population is very rare. Peptide receptor radionuclide therapy has shown benefit in metastatic gastroenteropancreatic neuroendocrine tumors (NETs) with an increasing interest in expanding its role as neoadjuvant treatment modality to improve the surgical candidature in inoperable NETs. There is currently no literature supporting its role in the pediatric NET patients. We present a rare case of a young boy with primary hepatic gastrinoma where 177Lu-based peptide receptor radionuclide therapy in the neoadjuvant setting contributed to his final disease-free status.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Gastrinoma / Neoplasias Primarias Secundarias / Tumores Neuroendocrinos Límite: Adult / Child / Humans / Male Idioma: En Revista: Clin Nucl Med Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Gastrinoma / Neoplasias Primarias Secundarias / Tumores Neuroendocrinos Límite: Adult / Child / Humans / Male Idioma: En Revista: Clin Nucl Med Año: 2024 Tipo del documento: Article