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一名17岁女性患者升结肠低分化黏液腺癌合并双侧卵巢成熟囊性畸胎瘤:病例报告

Poorly differentiated mucinous carcinoma of the ascending colon complicated by bilateral ovarian mature cystic teratomas in a 17-year-old female patient: a case report.

作者信息

Shimogawa Takuya, Hiyoshi Yukiharu, Ouchi Mayuko, Kosumi Keisuke, Eto Kojiro, Ida Satoshi, Iwatsuki Masaaki, Baba Yoshifumi, Miyamoto Yuji, Okazaki Nasa, Miyasato Yuko, Baba Hideo

机构信息

Department of Gastroenterological Surgery, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto, 860-8556, Japan.

Department of Diagnostic Pathology, Kumamoto University Hospital, 1-1-1 Honjo, Kumamoto, 860-8556, Japan.

出版信息

Surg Case Rep. 2024 Apr 23;10(1):95. doi: 10.1186/s40792-024-01892-z.

Abstract

BACKGROUND

Colorectal cancer (CRC) is one of the most common cancers worldwide, and screening colonoscopy has led to a decreasing incidence rate. However, the incidence of CRC is increasing among young people, especially adolescents and young adults (AYAs) who are not routinely screened. Although CRC is the fourth most common cancer among AYAs, it is extremely rare. In younger patients, CRC is often diagnosed later, and the proportion of patients with advanced CRC is higher than that in older patients. We herein present a case of poorly differentiated mucinous carcinoma of the ascending colon complicated by bilateral ovarian mature cystic teratomas (MCTs) in an AYA.

CASE PRESENTATION

A 17-year-old female patient presented with a chief complaint of abdominal pain and diarrhea that had persisted for more than 3 years. Colonoscopy revealed circumferential wall thickening of the ascending colon, and colonic biopsy revealed a mucous mass and findings of adenocarcinoma, predominantly signet ring cell carcinoma. Abdominal computed tomography (CT) and pelvic magnetic resonance imaging (MRI) showed bilateral ovarian tumors. Laparoscopic right hemicolectomy and enucleation of bilateral ovarian tumors were performed. Although the ascending colon cancer formed a large mass, there were no signs of peritoneal dissemination or direct invasion to the surrounding organs. Microscopically, the ascending colon was a poorly differentiated mucinous carcinoma with signet ring cell carcinoma and lymph node metastasis (9/42). The ovarian tumors were diagnosed as MCTs without any malignant components. The pathological diagnosis was ascending colon cancer (pT4aN2bM0, pStage IIIC) and bilateral ovarian MCTs. Microsatellite instability (MSI) testing was negative, and there were no gene mutations in either RAS or BRAF. Postoperative adjuvant chemotherapy with oxaliplatin and 5-FU was started.

CONCLUSIONS

We presented a case of locally advanced ascending colon cancer in a 17-year-old female patient. CRC rarely occurs in AYAs. However, the incidence has gradually increased in recent years. It should be considered as a differential diagnosis for young patients with long-term abdominal symptoms of unknown cause.

摘要

背景

结直肠癌(CRC)是全球最常见的癌症之一,筛查结肠镜检查已导致发病率下降。然而,CRC在年轻人中发病率正在上升,尤其是在未进行常规筛查的青少年和青年成年人(AYAs)中。尽管CRC是AYAs中第四常见的癌症,但极为罕见。在年轻患者中,CRC往往诊断较晚,晚期CRC患者的比例高于老年患者。我们在此报告一例AYA升结肠低分化黏液癌合并双侧卵巢成熟囊性畸胎瘤(MCTs)的病例。

病例介绍

一名17岁女性患者,主要症状为腹痛和腹泻,持续3年以上。结肠镜检查显示升结肠环形壁增厚,结肠活检显示黏液性肿块及腺癌表现,主要为印戒细胞癌。腹部计算机断层扫描(CT)和盆腔磁共振成像(MRI)显示双侧卵巢肿瘤。行腹腔镜右半结肠切除术及双侧卵巢肿瘤摘除术。尽管升结肠癌形成了一个大肿块,但没有腹膜播散或直接侵犯周围器官的迹象。显微镜下,升结肠为低分化黏液癌伴印戒细胞癌和淋巴结转移(9/42)。卵巢肿瘤诊断为MCTs,无任何恶性成分。病理诊断为升结肠癌(pT4aN2bM0,p分期IIIC期)和双侧卵巢MCTs。微卫星不稳定性(MSI)检测为阴性,RAS或BRAF均无基因突变。开始使用奥沙利铂和5-氟尿嘧啶进行术后辅助化疗。

结论

我们报告了一例17岁女性患者的局部晚期升结肠癌病例。CRC在AYAs中很少见。然而,近年来发病率逐渐上升。对于有长期不明原因腹部症状的年轻患者,应将其作为鉴别诊断之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f450/11039590/0ce5c776d001/40792_2024_1892_Fig1_HTML.jpg

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