Neuroendocrine tumors

Last revised by Michael P Hartung on 04 Feb 2022

Neuroendocrine tumors (NETs) (historically called APUDomas) represent a wide spectrum of disease. They consist of a large heterogeneous group of malignancies that are derived from embryonic neural crest tissue found in various organ such as the hypothalamus, pituitary gland, thyroid gland, adrenal medulla, and gastrointestinal tract. 

The spectrum of neuroendocrine tumors range from:

Pathology

They can also be divided by their biochemical behavior as functioning or non-functioning, by their aggressiveness as slow-growing and more aggressive lesions and so on.

Because of secretory products by amine precursor uptake and decarboxylation (APUD) they were historically known as APUDomas.

Genetics

Mostly occur sporadically, some are linked to multiple endocrine neoplasia syndromes.

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Cases and figures

  • Case 1 - gastric
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  • Case 2 - ileum
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  • Case 3 - pancreas
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