Department of Pathology, Shaoxing, Zhejiang, China.
Department of Gynecology, Shaoxing People's Hospital, Shaoxing, Zhejiang, China.
Medicine (Baltimore). 2023 Nov 17;102(46):e36170. doi: 10.1097/MD.0000000000036170.
The majority of rectal malignancies are primary tumors, secondary tumors are unusual. The rectal metastasis of endometrial carcinoma is reported to be extremely rare, especially in the absence of endometriosis.
Herein we present a rare case of a 68-year-old postmenopausal woman with a history of endometrial adenocarcinoma, metastasizing to the rectum 5 years after a hysterectomy and bilateral salpingo-oophorectomy treatments with pelvic lymphadenectomy were performed.
Histological examination of the rectal neoplasm revealed an invasive lesion in submucosal and muscular layers without definitely invaded evidence in the serous membrane and there was also no obvious endometriosis. The results of immunohistochemistry showed the cancer cells were positive for CK7, estrogen receptor, progesterone receptor, and negative for CK20, villin, confirming the diagnosis of metastatic rectal adenocarcinoma originating from uterine endometrial adenocarcinoma. Meanwhile, the results of immunohistochemical staining showed positive expression of MSH2, MSH6, and negative expression of MLH1 and PMS2, hinting at microsatellite instability which may be related to Lynch syndrome.
The Dixon operation with lymph node dissection was performed. Chemotherapy was also performed on this patient for the next 6 months.
The patient was followed up for the next 6 months after surgery and no recurrence was documented until now.
Though rectal and endometrial adenocarcinoma could share some similar morphologic features, different immunohistochemical profiles could be revealed between them. Most endometrial carcinoma in the colon or rectum develop from endometriosis. Secondary rectal cancer with endometrial origination in the absence of endometriosis and serosal implants was extremely rare. Therefore, we should pay more attention to this rare but possible presentation for appropriate diagnosis and treatment of these patients.
大多数直肠恶性肿瘤为原发性肿瘤,继发性肿瘤不常见。子宫内膜癌直肠转移报道极为罕见,特别是在无子宫内膜异位症的情况下。
本文报告了 1 例罕见病例,1 名 68 岁绝经后妇女,既往有子宫内膜腺癌病史,在子宫切除术和双侧输卵管卵巢切除术以及盆腔淋巴结清扫术后 5 年,直肠转移。
直肠肿瘤的组织学检查显示黏膜下和肌层的侵袭性病变,浆膜无明确侵犯证据,也无明显的子宫内膜异位症。免疫组织化学结果显示癌细胞 CK7、雌激素受体、孕激素受体阳性,CK20、villin 阴性,证实为转移性直肠腺癌,来源于子宫子宫内膜腺癌。同时,免疫组化染色结果显示 MSH2、MSH6 阳性,MLH1、PMS2 阴性,提示微卫星不稳定,可能与 Lynch 综合征有关。
进行 Dixon 手术和淋巴结清扫术。对该患者进行了 6 个月的化疗。
患者术后随访 6 个月,目前未见复发。
虽然直肠腺癌和子宫内膜腺癌可能具有一些相似的形态特征,但它们的免疫组织化学特征可能不同。大多数结肠癌或直肠癌的子宫内膜癌来源于子宫内膜异位症。在无子宫内膜异位症和浆膜种植的情况下,罕见发生源自子宫内膜的继发性直肠肿瘤。因此,我们应该更加注意这种罕见但可能出现的表现,以便对这些患者进行适当的诊断和治疗。