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阿卡迪·M·里夫林国际病理切片俱乐部精选病例:一名年轻女孩的横结肠癌。

Selected case from the Arkadi M. Rywlin International Pathology Slide Club: carcinoma of the transverse colon in a young girl.

作者信息

Galliani Carlos A, Sanchez Irene C, D'Errico Maria M, Bisceglia Michele

机构信息

*Department of Pathology, Children's Hospitals and Clinics of Minnesota, Minneapolis, MN †Department of Pathology, Cook Children's Medical Center, Fort Worth, TX ‡School of Medicine, University of Milan, Milan §School of Biomedical Sciences, Etromapmacs Pole, Lesina (FG), Italy.

出版信息

Adv Anat Pathol. 2015 May;22(3):217-24. doi: 10.1097/PAP.0000000000000068.

Abstract

We report a case of a 14-year-old female with primary adenocarcinoma of the transverse colon. She was hospitalized after presenting with abdominal pain and signs of intestinal obstruction. There was no health antecedent or family history of neoplasia. Physical examination revealed a distended abdomen. Tenderness was elicited to palpation of the right lower quadrant. Magnetic resonance imaging of the abdomen revealed obstructive signs, with a constricting lesion in the mid-transverse colon of probable neoplastic nature. Laparoscopic segmental resection of the colon was followed by standard right hemicolectomy. A circumferential mid-transverse tumor was diagnosed as primary colorectal carcinoma (CRC) of signet-ring cell type, AJCC stage IIIC, Dukes' C stage. On the basis of immunohistochemistry and clinical data, hereditary nonpolyposis and hamartomatous colorectal cancer syndromes were excluded. Involvement of either the p53, BRAF, or K-RAS genes was ruled out by immunohistochemistry profiling and genetic testing. The neoplasm was categorized as sporadic. The possibility of activation of the Wnt signaling pathway was suspected, because of a defective turnover of the β-catenin protein. Postoperatively, the patient was treated with both systemic and intra-abdominal adjuvant chemotherapy, including oxaliplatin. Between 18 and 24 months after diagnosis, intra-abdominal tumor recurrences were detected. The patient underwent bilateral oophorectomies for Krukenberg tumors and received salvage chemotherapy. Recently, additional recurrent metastatic retroperitoneal disease caused hydronephrosis. The retroperitoneal mass was debulked and a ureteric stent was placed. At the time of this writing, 43 months after diagnosis, the patient is receiving FOLFOX chemotherapy combined with panitumumab. CRC of childhood is exceedingly rare, generally develops in the setting of unrecognized genetic predisposing factors to cancer, presents with advanced disease, is high grade, and tends to have dismal prognosis.

摘要

我们报告一例14岁女性原发性横结肠癌病例。她因腹痛和肠梗阻症状入院。无健康问题史或肿瘤家族史。体格检查发现腹部膨隆。右下腹触诊有压痛。腹部磁共振成像显示有梗阻征象,横结肠中部有一狭窄病变,可能为肿瘤性质。先行腹腔镜结肠节段切除术,随后进行标准的右半结肠切除术。一个环绕横结肠中部的肿瘤被诊断为印戒细胞型原发性结直肠癌(CRC),美国癌症联合委员会(AJCC)IIIC期,杜克(Dukes)C期。根据免疫组化和临床资料,排除遗传性非息肉病和错构瘤性结直肠癌综合征。通过免疫组化分析和基因检测排除了p53、BRAF或K-RAS基因的受累。该肿瘤被归类为散发性。由于β-连环蛋白的周转缺陷,怀疑Wnt信号通路被激活。术后,患者接受了全身和腹腔内辅助化疗,包括奥沙利铂。在诊断后的18至24个月之间,检测到腹腔内肿瘤复发。患者因库肯勃瘤接受了双侧卵巢切除术并接受了挽救性化疗。最近,额外的复发性腹膜后转移疾病导致肾积水。对腹膜后肿块进行了减瘤手术并放置了输尿管支架。在撰写本文时,诊断后43个月,患者正在接受FOLFOX化疗联合帕尼单抗治疗。儿童CRC极为罕见,通常在未被认识的癌症遗传易感性因素背景下发生,表现为晚期疾病,分级高,预后往往不佳。

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