Colorectal adenocarcinoma in children and adolescents.

R Bigliardi, M Morici, G Messere, G Ortiz, J Fernandez, A Varela, J Vidal, F Diaz, J Salas, M C Riccheri
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Abstract

Introduction: Colorectal adenocarcinoma is rare in children and adolescents and tends to present with nonspecific signs and symptoms, leading to late diagnoses.

Objectives: Our aim was to describe the clinical presentation and progression in children and adolescents with colorectal adenocarcinoma treated at our hospital and detect possible predisposing conditions of this disease.

Materials and methods: Eight patients with colorectal adenocarcinoma were followed at the Hospital Posadas within the time frame of January 2000 and December 2021. We searched for diseases predisposing to this cancer.

Results: The mean patient age was 16 years (between 11 and 17 years of age). Clinical presentation was abdominal pain in the 8 patients; 4 of them had pain in the right hypochondrium, 3 had abdominal tumor, 4 had rectal bleeding, and 3 had weight loss. Mean symptom duration was 9 weeks (range: 1-24 weeks). None of the patients showed predisposing illnesses. One patient presented with polyposis, with no cases in any other family member. Histology showed mucinous adenocarcinoma in all the patients, 4 of whom had the signet ring cell subtype. The primary tumor was located in the right colon in 6 patients. At diagnosis, staging according to the modified Dukes classification was: I: one patient; IIb: one patient; IIIb: one patient; IIIc: one patient; and IV: 4 patients. All patients except 2 received chemotherapy and one patient received radiotherapy. Overall survival at 3 years was 25%.

Conclusions: All patients presented with mucinous adenocarcinoma, no predisposing diseases were found, and the children with colorectal cancer had a very poor prognosis. Colorectal cancer diagnosis should be considered in children presenting with acute abdominal pain, abdominal tumor, or lower gastrointestinal bleeding, especially if there is weight loss.

儿童和青少年结直肠腺癌。
导言:结直肠腺癌在儿童和青少年中非常罕见,往往表现为非特异性症状和体征,导致诊断较晚:我们的目的是描述在我院接受治疗的儿童和青少年结直肠腺癌患者的临床表现和病情发展,并检测该疾病可能的易感因素:波萨达斯医院在2000年1月至2021年12月期间对8名结直肠腺癌患者进行了随访。结果:患者的平均年龄为 16 岁(16 岁以下):患者平均年龄为16岁(11至17岁)。8名患者的临床表现为腹痛,其中4人右下腹疼痛,3人腹部肿瘤,4人直肠出血,3人体重减轻。平均症状持续时间为 9 周(范围:1-24 周)。所有患者均无诱发疾病。其中一名患者患有息肉病,其他家庭成员中没有病例。组织学检查显示,所有患者均为黏液腺癌,其中 4 人属于标志环细胞亚型。6 名患者的原发肿瘤位于右侧结肠。确诊时,根据修改后的杜克斯分类法进行了分期:I期:1名患者;IIb期:1名患者;IIIb期:1名患者;IIIc期:1名患者;IV期:4名患者。除 2 名患者外,其他患者均接受了化疗,1 名患者接受了放疗。3年的总生存率为25%:结论:所有患者均为粘液腺癌,未发现诱发疾病,儿童结直肠癌患者预后极差。如果儿童出现急性腹痛、腹部肿瘤或下消化道出血,尤其是体重减轻,应考虑诊断为结直肠癌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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