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Large primary hepatic gastrinoma in young patient treated with trisegmentectomy: A case report and review of the literature

Primary hepatic gastrinoma is a rare disease, with fewer than 40 cases reported in the medical literature. Because it is located in an organ in which metastases are common, its diagnosis is difficult. We report a case of a 19 years old male patient with a history of gastric ulcers since the age of n...

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Detalles Bibliográficos
Autores principales: Pipek, Leonardo Zumerkorn, Jardim, Yuri Justi, de Mesquita, Gustavo Heluani Antunes, Nii, Fernanda, Medeiros, Kayo Augusto de Almeida, Carvalho, Bárbara Justo, Martines, Diego Ramos, Iuamoto, Leandro Ryuchi, Waisberg, Daniel Reis, D’Albuquerque, Luiz Augusto Carneiro, Meyer, Alberto, Andraus, Wellington
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068851/
https://www.ncbi.nlm.nih.gov/pubmed/30079138
http://dx.doi.org/10.4254/wjh.v10.i7.517
Descripción
Sumario:Primary hepatic gastrinoma is a rare disease, with fewer than 40 cases reported in the medical literature. Because it is located in an organ in which metastases are common, its diagnosis is difficult. We report a case of a 19 years old male patient with a history of gastric ulcers since the age of nine. Following gastric surgery, an antrectomy and a vagotomy, there was some alleviation of symptoms. Subsequently, the patient reported various intermittent episodes of diarrhea, diffuse abdominal pain, and vomiting. The patient underwent tomography, which revealed the presence of a hepatic mass measuring 19.5 cm × 12.5 cm × 17 cm. Primary hepatic gastrinoma was diagnosed based on laboratory examinations that indicated hypergastrinemia and a positron emission tomography/magnetic resonance study with somatostatin analogue that confirmed the liver as the primary site. After hepatic trisegmentectomy (II, III, IV, V, VIII), the patient’s symptoms improved. The case is notable for the presence of a rare tumor with uncommon dimensions.