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Rev Esp Med Nucl Imagen Mol ; 32(2): 107-10, 2013 Mar.
Artículo en Español | MEDLINE | ID: mdl-23099067

RESUMEN

Multiple Endocrine Neoplasia type 1 syndrome (MEN1) is characterized by the presence of tumors in parathyroid glands, anterior pituitary gland, endocrine pancreas and duodenum. However, other tumors may also occur. One of them is the carcinoid tumor, which in this context, is more common in the gastrointestinal tract. Less common is the presence of carcinoid tumors of bronchial origin, which with histologic confirmation, may occur in 5-8% of cases and that appears more frequently in patients with hypergastrinemia. We report a patient with MEN1 syndrome, hypergastrinemia and an incidental finding in a somatostatin receptor scintigraphy of an unsuspected bronchial carcinoid tumor that was confirmed histologically.


Asunto(s)
Neoplasias de los Bronquios/complicaciones , Neoplasias de los Bronquios/diagnóstico por imagen , Tumor Carcinoide/complicaciones , Tumor Carcinoide/diagnóstico por imagen , Gastrinas/sangre , Neoplasia Endocrina Múltiple Tipo 1/complicaciones , Neoplasias Primarias Múltiples/complicaciones , Receptores de Somatostatina , Adulto , Humanos , Hallazgos Incidentales , Masculino , Cintigrafía , Receptores de Somatostatina/análisis
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