Somatostatinoma (Q87577): Difference between revisions

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Tumor neuroendócrino raro, geralmente maligno, originado de células delta. Essa neoplasia produz grandes quantidades de somatostatina, que pode resultar em uma síndrome caracterizada por diarreia, esteatorreia, perda de peso e hipossecreção gástrica. Sessenta por cento são encontrados no pâncreas e 40% no duodeno ou jejuno. O pico de incidência ocorre entre 40 e 60 anos de idade; as mulheres são afetadas mais do que os homens em 2:1.
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A rare, usually malignant neuroendocrine tumour arizing from delta cells. This neoplasm produces large amounts of somatostatin, which may result in a syndrome characterised by diarrhea, steatorrhea, weight loss, and gastric hyposecretion. Sixty percent are found in the pancreas and 40% in the duodenum or jejunum. The peak incidence occurs between 40 and 60 years of age; women are affected more than men by 2:1.

Revision as of 13:15, 15 August 2026

A rare, usually malignant neuroendocrine tumour arizing from delta cells. This neoplasm produces large amounts of somatostatin, which may result in a syndrome characterised by diarrhea, steatorrhea, weight loss, and gastric hyposecretion. Sixty percent are found in the pancreas and 40% in the duodenum or jejunum. The peak incidence occurs between 40 and 60 years of age; women are affected more than men by 2:1.
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ID_219879696
    English
    Somatostatinoma
    A rare, usually malignant neuroendocrine tumour arizing from delta cells. This neoplasm produces large amounts of somatostatin, which may result in a syndrome characterised by diarrhea, steatorrhea, weight loss, and gastric hyposecretion. Sixty percent are found in the pancreas and 40% in the duodenum or jejunum. The peak incidence occurs between 40 and 60 years of age; women are affected more than men by 2:1.

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