Ariani Gusti Deasy Wilda, Faruk Muhammad
Division of Digestive, Department of Surgery, Faculty of Medicine, Hasanuddin University Makassar, Indonesia.
Division of Oncology, Department of Surgery, Faculty of Medicine, Hasanuddin University Makassar, Indonesia.
Int J Surg Case Rep. 2020;72:411-417. doi: 10.1016/j.ijscr.2020.06.030. Epub 2020 Jun 12.
Neuroendocrine tumors (NET) of the colon and sigmoid colon are uncommon compared to colorectal adenocarcinoma. Few reports have been made of NET of the colon and sigmoid colon that presents with peritonitis and large bowel obstruction.
Here, we report two cases of NET of the colon and sigmoid colon, which were diagnosed and treated at our institution. In our first case, a 66-year-old man with a history of abdominal distension was diagnosed with NET via histopathology of the sigmoid colon. The second case involved a 45-year-old woman with the chief complaints of abdominal distention and inability to defecate; specimen histopathology of the descending colon showed neuroendocrine carcinoma features. Clinical outcome was very poor in our patients: eight months after the resection, the second patient demonstrated a sign of metastasis on the liver.
An uncommon case of colon and sigmoid colon carcinoma with neuroendocrine and diagnostic difficulties precludes an exact description of the initial diagnostic criteria and management. Thus, our case series offers an overview of initial symptoms, radiological and histopathological features for early diagnosis, and proper management of NET.
与结直肠癌相比,结肠和乙状结肠的神经内分泌肿瘤(NET)并不常见。关于以腹膜炎和大肠梗阻为表现的结肠和乙状结肠NET的报道很少。
在此,我们报告两例在我院诊断和治疗的结肠和乙状结肠NET病例。第一例,一名有腹胀病史的66岁男性通过乙状结肠组织病理学诊断为NET。第二例,一名45岁女性,主要症状为腹胀和无法排便;降结肠标本组织病理学显示神经内分泌癌特征。我们的患者临床结局很差:切除术后八个月,第二名患者出现肝脏转移迹象。
结肠和乙状结肠神经内分泌癌这一罕见病例及诊断困难使得无法准确描述初始诊断标准和治疗方法。因此,我们的病例系列提供了有关初始症状、用于早期诊断的放射学和组织病理学特征以及NET正确治疗方法的概述。