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Neuroendocrine Carcinomas of the Colon and Rectum

Diseases of the Colon & Rectum · 2004 · Vol. 47(2) · pp. 163–169
Paul E. BernickDavid S. KlimstraJinru ShiaBruce D. MinskyLeonard B. SaltzWei ShiHoward T. ThalerJosé G. GuillemPhilip B. PatyA. M. CohenW. Douglas Wong

Abstract

Neuroendocrine carcinomas of the colon and rectum are uncommon, comprising less than 1 percent of colon and rectal cancers. Pathologically, these tumors are poorly differentiated carcinomas with distinctive cytoarchitectural features and are often immunoreactive for markers of neuroendocrine differentiation. The prognosis for high-grade neuroendocrine carcinomas is poor, as most patients have metastatic disease at the time of diagnosis.

Colorectal and Anal CarcinomasNeuroendocrine Tumor Research AdvancesMetastasis and carcinoma case studiesMedicineRectumSurgical oncologyColorectal surgeryGeneral surgeryInternal medicineOncologyAbdominal surgery

MeSH terms

AdultAgedAged, 80 and overBiopsyColonic NeoplasmsFemaleHumansMaleMiddle AgedNeoplasm MetastasisNeoplasm StagingPrognosisRectal NeoplasmsRetrospective StudiesBiomarkers, Tumor
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