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结肠管状腺瘤与神经内分泌癌并存,可进行早期手术干预,提示存在共同的干细胞起源。

Coexisting tubular adenoma with a neuroendocrine carcinoma of colon allowing early surgical intervention and implicating a shared stem cell origin.

作者信息

Soliman Mahmoud L, Tiwari Ashish, Zhao Qing

机构信息

Mahmoud L Soliman, Qing Zhao, Department of Pathology and Laboratory Medicine, Boston University Medical Center, Boston, MA 02118, United States.

出版信息

World J Gastroenterol. 2017 Feb 14;23(6):1106-1112. doi: 10.3748/wjg.v23.i6.1106.

Abstract

High-grade colonic neuroendocrine carcinomas (NECs) are uncommon but extremely aggressive. Their co-existence with tubular adenoma (TA) has rarely been reported. We present a 68-year-old man who was found on routine colonoscopy to have multiple colorectal TAs and an ulcerated lesion in the ascending colon. Microscopically, a poorly-differentiated invasive carcinoma juxtaposed with a TA was identified. Differential diagnosis included a poorly-differentiated adenocarcinoma, medullary carcinoma, high-grade NEC and lymphoma. The immunohistochemical profile showed positive staining for keratins, synaptophysin and chromogranin but negative for LCA, CDX2, CK7, CK20, TTF-1 and PSA, supporting the NEC diagnosis. Upon subsequent laparoscopic right hemicolectomy, the tumor was identified as a 3.0 cm umbilicated and ulcerated mass with an adjacent TA. Both TA and NEC showed positive staining for β-catenin indicating a shared colonic origin. The mitotic counts (77/10 high power fields) and a high proliferation rate (75% by Ki-67) corroborated a high-grade stratification. Mutational analysis indicated a wild-type and with mismatch repair proficiency. The AJCC (7 edition) pathologic stage is pT3, pN0, pMx. The patient received adjuvant chemotherapy with cisplatin/etoposides for three cycles and will be followed up for a year to detect recurrence. In conclusion, the co-existence of TA with high grade-NEC in our case allowed early identification and intervention of the otherwise asymptomatic but aggressive tumor. In addition, the finding of a high-grade NEC within a large TA in this case suggests a link between the two lesions and could represent a shared stem cell origin.

摘要

高级别结肠神经内分泌癌(NECs)并不常见,但极具侵袭性。其与管状腺瘤(TA)并存的情况鲜有报道。我们报告一名68岁男性,在常规结肠镜检查中发现有多个结直肠TA以及升结肠的一个溃疡性病变。显微镜下,发现一个与TA并列的低分化浸润性癌。鉴别诊断包括低分化腺癌、髓样癌、高级别NEC和淋巴瘤。免疫组化结果显示角蛋白、突触素和嗜铬粒蛋白染色阳性,但淋巴细胞共同抗原(LCA)、尾型同源盒转录因子2(CDX2)、细胞角蛋白7(CK7)、细胞角蛋白20(CK20)、甲状腺转录因子1(TTF-1)和前列腺特异性抗原(PSA)染色阴性,支持NEC的诊断。随后行腹腔镜右半结肠切除术,肿瘤为一个3.0 cm的脐状溃疡性肿块,伴有一个相邻的TA。TA和NEC的β-连环蛋白染色均为阳性,表明它们有共同的结肠起源。有丝分裂计数(77/10个高倍视野)和高增殖率(Ki-67为75%)证实为高级别分层。突变分析显示为野生型且错配修复功能正常。美国癌症联合委员会(第7版)病理分期为pT3、pN0、pMx。患者接受了三个周期的顺铂/依托泊苷辅助化疗,并将随访一年以检测复发情况。总之,在我们的病例中TA与高级别NEC并存,使得原本无症状但具有侵袭性的肿瘤得以早期识别和干预。此外,在本例一个大的TA内发现高级别NEC提示这两种病变之间存在联系,可能代表共同的干细胞起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4179/5311100/e263b20c95ec/WJG-23-1106-g001.jpg

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