Angelini Carlo, Crippa Stefano, Uggeri Fabio, Bonardi Claudia, Sartori Paola, Uggeri Franco
Department of Surgery, University of Milan-Bicocca, San Gerardo Hospital, Monza, MI, Italy.
Pediatr Surg Int. 2005 Oct;21(10):839-40. doi: 10.1007/s00383-005-1525-3. Epub 2005 Oct 21.
Colorectal cancer is extremely rare in children and presents with a poor prognosis because of the delay in diagnosis and lack of histological differentiation. We report a case of a sigmoid colon carcinoma with areas of neuroendocrine cells in a 12-year-old patient without familial occurrence of colorectal cancer. Symptoms at presentation were anaemia, anorexia, abdominal pain and weight loss. The patient was treated with radical resection and adjuvant chemotherapy. One year later, a local recurrence and hepatic metastases were diagnosed and she underwent chemotherapy and surgical resection. Twenty-six months from initial diagnosis she is alive with evidence of disease. The clinical presentation, diagnosis and treatment of the previously reported cases of colorectal cancer in children are also reviewed.
结直肠癌在儿童中极为罕见,由于诊断延迟和缺乏组织学分化,其预后较差。我们报告一例12岁乙状结肠癌患者,该患者无结直肠癌家族史,肿瘤存在神经内分泌细胞区域。患者就诊时的症状为贫血、厌食、腹痛和体重减轻。患者接受了根治性切除和辅助化疗。一年后,诊断出局部复发和肝转移,她接受了化疗和手术切除。自初次诊断起26个月后,她仍存活但有疾病证据。本文还回顾了先前报道的儿童结直肠癌病例的临床表现、诊断和治疗情况。