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ABSTRACT
Multiple endocrine neoplasia type 1 (MEN1) syndrome is characterized by combined occurrence of tumors of endocrine glands including the parathyroid, the pancreatic islet cells, and the anterior pituitary gland. Parathyroid involvement is the most common manifestation and usually the first clinical involvement inMEN1 syndrome, followed by gastroentero-pancreatic neuroendocrine tumors (NETs). Here we present a case where the patient initially presented with metastatic gastric NET and a single parathyroid adenoma was detected incidentally on ⁶⁸Ga-DOTANOC PET/CT done as part of post ¹⁷⁷Lu-DOTATATE therapy (PRRT) follow-up. Further ¹⁸F-fluorocholine PET/CT showed four adenomas for which the patient subsequently underwent subtotal parathyroidectomy.
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Texto completo: 1 Índice: WPRIM Assunto principal: Neoplasias das Paratireoides / Adeno-Hipófise / Somatostatina / Gastrinoma / Adenoma / Seguimentos / Paratireoidectomia / Ilhotas Pancreáticas / Receptores de Somatostatina / Tumores Neuroendócrinos Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Korean Journal of Nuclear Medicine Ano de publicação: 2018 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Neoplasias das Paratireoides / Adeno-Hipófise / Somatostatina / Gastrinoma / Adenoma / Seguimentos / Paratireoidectomia / Ilhotas Pancreáticas / Receptores de Somatostatina / Tumores Neuroendócrinos Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Korean Journal of Nuclear Medicine Ano de publicação: 2018 Tipo de documento: Article