Small cell carcinoma (SCC) is a rare malignancy that can affect the gastrointestinal tract. Current knowledge is limited to individual case series. Here we present three cases from our own institution and report the results of a systematic review of the literature.
Methods and findings: A ten-year review of our institutions pathology database for rectal SCC was performed. A systematic search of Embase, PubMed and Google Scholar with cross-referencing was performed applying suitable exclusion criteria. Three cases were identified in our institution from 2004-2014. All were positive for synaptophysin, TTF-1, CD56 and CK positive. All had metastatic disease at presentation and had chemoradiotherapy. Median survival was 13 months. A systematic search found 112 articles of which 41 were included (121 patients). Optimal survival (37 months) was observed with a combination of surgery, chemotherapy and radiotherapy.
Conclusion: SCC rectum is a rare entity that is usually metastatic at presentation and has poor long-term survival despite aggressive treatment schedules. Prospective registries would optimize management of this unusual neuroendocrine tumour.
Qasem E, Nangalia M, Jones H, Griffiths P, Sekaran C, Evans MD, Davies M, Khot U, Beynon J, Williams N and Harris DA
Colorectal Cancer: Open Access received 92 citations as per google scholar report