Khan Muhammad, Dirweesh Ahmed, Alvarez Chikezie, Conaway Herbert, Moser Robert
Department of Internal Medicine, Saint Francis Medical Center, Seton Hall University, Trenton, NJ, USA.
Department of Pathology, Saint Francis Medical Center, Trenton, NJ, USA.
Gastroenterology Res. 2017 Feb;10(1):56-58. doi: 10.14740/gr751w. Epub 2017 Feb 21.
Neuroendocrine tumors in gastrointestinal (GI) tract are a rare source of GI malignancy with an estimated incidence of 2.5 - 5 per 100,000 people per year and the prevalence of 35 per 100,000. In the GI tract, they are located in decreasing order of frequency in appendix, ileum, rectum, stomach, and colon. Those found in the anal region represent just 1% of all malignancies of the anal canal. Their clinical presentation can be widely varying, sometimes being found incidentally with metastatic disease and an unknown primary source. We report a case of a 60-year-old male who presented with a 2-week history of intermittent bright red blood per rectum and anal pain. He was found to have a lesion in the perianal area which was subsequently diagnosed has a poorly differentiated large cell type neuroendocrine carcinoma (NEC) with hepatic metastasis.
胃肠道神经内分泌肿瘤是胃肠道恶性肿瘤的罕见来源,估计每年发病率为每10万人2.5至5例,患病率为每10万人35例。在胃肠道中,它们按频率递减顺序位于阑尾、回肠、直肠、胃和结肠。在肛门区域发现的那些肿瘤仅占肛管所有恶性肿瘤的1%。它们的临床表现差异很大,有时偶然发现伴有转移性疾病且原发灶不明。我们报告一例60岁男性,有两周间歇性便血和肛门疼痛病史。他被发现肛周区域有一个病变,随后被诊断为低分化大细胞型神经内分泌癌(NEC)伴肝转移。