Shimura Taiga, Fukushima Naoko, Tsuboi Kazuto, Suzuki Toshimasa, Kajimoto Tetsuya
Department of Surgery, Fuji General Hospital, Shizuoka, Japan.
Department of Surgery, The Jikei University School of Medicine, Tokyo, Japan.
Surg Case Rep. 2024 Nov 28;10(1):273. doi: 10.1186/s40792-024-02073-8.
The majority of colorectal malignancies are primary tumors. Secondary tumors are rare, and colorectal metastasis from endometrial carcinoma is exceptionally uncommon. We report a case of serous endometrial carcinoma that metastasized to the sigmoid colon, initially presenting as a primary colon carcinoma due to bowel obstruction.
A 79-year-old woman presented with abdominal distention and constipation. Five years earlier, she had undergone an open total hysterectomy with bilateral salpingo-oophorectomy for endometrial serous carcinoma. A colonoscopy revealed stenosis encircling the entire sigmoid colon. Abdominal computed tomography demonstrated irregular wall thickening in the sigmoid colon with enhanced regional lymph node enlargement and upstream bowel dilatation. Peritoneal dissemination in the pelvis was also noted. To relieve the obstruction, two self-expanding metal stents were inserted. Subsequently, due to the presumed diagnosis of sigmoid colon carcinoma with peritoneal dissemination, an open left hemicolectomy with resection of the peritoneal dissemination was performed. Histopathological examination identified the colon tumor and peritoneal dissemination as metastatic serous endometrial carcinoma. Immunohistochemical studies showed the tumor cells were negative for CK7, CK20, and CDX2. No chemotherapy was administered, and 6 months post-operation, no recurrence was observed.
Metastasis of endometrial carcinoma to the colon is extremely rare. Diagnosing a colon tumor as a metastasis from endometrial carcinoma is challenging during preoperative examinations. Therefore, in patients with a history of endometrial carcinoma, the possibility that the primary site might be the uterus should be considered.
大多数结直肠恶性肿瘤为原发性肿瘤。继发性肿瘤罕见,子宫内膜癌转移至结直肠极为少见。我们报告一例浆液性子宫内膜癌转移至乙状结肠的病例,该病例最初因肠梗阻表现为原发性结肠癌。
一名79岁女性因腹胀和便秘就诊。5年前,她因子宫内膜浆液性癌接受了开放性全子宫切除术及双侧输卵管卵巢切除术。结肠镜检查发现整个乙状结肠有环形狭窄。腹部计算机断层扫描显示乙状结肠壁不规则增厚,区域淋巴结肿大且上游肠管扩张。盆腔内也发现了腹膜播散。为缓解梗阻,插入了两个自膨式金属支架。随后,由于推测诊断为乙状结肠癌伴腹膜播散,进行了开放性左半结肠切除术及腹膜播散病灶切除术。组织病理学检查确定结肠肿瘤和腹膜播散为转移性浆液性子宫内膜癌。免疫组织化学研究显示肿瘤细胞CK7、CK20和CDX2均为阴性。未给予化疗,术后6个月未观察到复发。
子宫内膜癌转移至结肠极为罕见。在术前检查中将结肠肿瘤诊断为子宫内膜癌转移具有挑战性。因此,对于有子宫内膜癌病史的患者,应考虑原发部位可能是子宫的可能性。