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Colorectal neuroendocrine tumor is a recently recognized malignancy that occurs sporadically or in association with hereditary syndromes (familial medullary carcinoma of the thyroid). In the sporadic cases, this tumor typically occurs in older adults and has a favorable prognosis after complete surgical resection, although distant metastases are common. In the familial form of this disease, the carcinomas arise in the setting of the associated endocrine disorders, such as multiple endocrine neoplasia (MEN) type 1 and 2, and familial adenomatous polyposis (FAP). The role of somatostatin analogs in the management of these patients is unclear. The histopathological characteristics of this tumor are also distinct from those of the commonly encountered colorectal adenocarcinoma and poorly differentiated carcinoma, and its distinction from metastatic deposits of well-differentiated neuroendocrine tumors from the lung is imperative. The authors present a series of five tumors with dual neuroendocrine and adenocarc

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