Rectal Neuroendocrine Tumours

Česká verze

Authors: O. Louthan
Authors place of work: IV. interní klinika 1. lékařské fakulty UK a VFN, Praha
Published in the journal: Klin Onkol 2009; 22(5): 195-201
Category: Přehledy

Summary

Rectal neuroendocrine tumours (carcinoids) belong to the hindgut carcinoid group, according to older classification. They are not associated with carcinoid syndrome. Colonoscopy is a gold standard for detecting rectal carcinoids. Endosonography is important for assessing rectal carcinoid growth. CT colonography and 111In-octreotide scanning is required for staging if residual or metastatic disease is suspected. Serum chromogranin A and acid phosphatase are necessary biochemical markers. Local resection is sufficient for small tumours, anterior resection for rectal tumours > 2cm is appropriate. There is no evidence base for adjuvant therapy. Patients with rectal carcinoids < 2cm have a very good prognosis with long term survival.

Key words:
carcinoid –⁠ rectal cancer –⁠ chromogranin A –⁠ OctreoScan –⁠ endosonography –⁠ therapy

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