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子宫下段和宫颈管上皮样滋养细胞肿瘤:一例报告

Epithelioid trophoblastic tumor of the lower uterine segment and cervical canal: A case report.

作者信息

Yuan Ling-Qin, Hao Ting, Pan Guo-You, Guo Hui, Li Da-Peng, Liu Nai-Fu

机构信息

Department of Gynecologic Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan 250117, Shandong Province, China.

Department of Pathology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan 250117, Shandong Province, China.

出版信息

World J Clin Cases. 2023 Feb 6;11(4):938-944. doi: 10.12998/wjcc.v11.i4.938.

Abstract

BACKGROUND

Epithelioid trophoblastic tumor (ETT) is the rarest type of gestational trophoblastic tumor (GTT). It has been reported that more than 50% of ETTs arise in the uterine cervix or the lower uterine segment. Here, we report a case of ETT within the lower uterine segment and cervical canal and discuss its manifestations, possible causes, and related influencing factors.

CASE SUMMARY

A 35-year-old woman (gravida 7, miscarriage 3, induction 2 with 1 being twins, para 2 of cesarean section, live 2), who had amenorrhea for 9 mo after breastfeeding for 22 mo after the last cesarean section, was diagnosed with ETT. The lesion was present in the lower uterine segment and endocervical canal with severe involvement of the anterior wall of the lower uterine segment and the front wall of the lower uterine segment where the cesarean incisions were made. Laboratory tests showed slight elevation of serum beta-human chorionic gonadotropin. Intraoperative exploration showed the presence of a normal-sized uterus body with an enlarged tumor in the lower uterine segment. The surface of the lower uterine segment was light blue, the entire lesion was approximately about 8 cm × 8 cm × 9 cm, with compression and displacement of the surrounding tissue. Histological examination diagnosed ETT. Immunohistochemical analysis showed positive expression of p63, with a Ki-67 proliferation index of 40%.

CONCLUSION

A search of the PubMed database using the search terms "cesarean section" and "epithelioid trophoblastic tumor" retrieved nine articles, including 13 cases of ETT and ETT-related lesions, all 13 cases had a history of cesarean section, and the lesions were all located at the cesarean section incision on the anterior wall of the lower uterine segment. The present case is the 14th reported case of ETT after cesarean section. Therefore, we deduced that cesarean section trauma had an important effect on the occurrence of ETT at this site.

摘要

背景

上皮样滋养细胞肿瘤(ETT)是妊娠滋养细胞肿瘤(GTT)中最罕见的类型。据报道,超过50%的ETT发生于子宫颈或子宫下段。在此,我们报告一例发生于子宫下段和宫颈管的ETT病例,并讨论其临床表现、可能病因及相关影响因素。

病例摘要

一名35岁女性(孕7产2,流产3次,引产2次,其中1次为双胎,剖宫产2次,存活2胎),末次剖宫产术后母乳喂养22个月,停经9个月,被诊断为ETT。病变位于子宫下段和宫颈管,子宫下段前壁及剖宫产切口所在的子宫下段前壁严重受累。实验室检查显示血清β-人绒毛膜促性腺激素轻度升高。术中探查发现子宫体大小正常,子宫下段有一增大的肿瘤。子宫下段表面呈浅蓝色,整个病变约8 cm×8 cm×9 cm,周围组织受压移位。组织学检查诊断为ETT。免疫组化分析显示p63阳性表达,Ki-67增殖指数为40%。

结论

在PubMed数据库中使用检索词“剖宫产”和“上皮样滋养细胞肿瘤”进行检索,共检索到9篇文章,包括13例ETT及ETT相关病变,所有13例均有剖宫产史,病变均位于子宫下段前壁的剖宫产切口处。本病例是第14例报道的剖宫产术后ETT病例。因此,我们推断剖宫产创伤对该部位ETT的发生有重要影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b042/9928694/ef62b03c05d8/WJCC-11-938-g001.jpg

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