Your browser doesn't support javascript.
loading
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.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Parathyroid Neoplasms / Pituitary Gland, Anterior / Somatostatin / Gastrinoma / Adenoma / Follow-Up Studies / Parathyroidectomy / Islets of Langerhans / Receptors, Somatostatin / Neuroendocrine Tumors Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Korean Journal of Nuclear Medicine Year: 2018 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Parathyroid Neoplasms / Pituitary Gland, Anterior / Somatostatin / Gastrinoma / Adenoma / Follow-Up Studies / Parathyroidectomy / Islets of Langerhans / Receptors, Somatostatin / Neuroendocrine Tumors Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Korean Journal of Nuclear Medicine Year: 2018 Document type: Article
...