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非典型胎盘部位结节:5例报告及文献复习

Atypical placental site nodules: Five cases and literature review.

作者信息

He Yifu, Yang Wenqing, Zhang Yu

机构信息

Department of Gynecology, Xiangya Hospital, Central South University, Changsha 410008.

Gynecological Oncology Research and Engineering Center of Hunan Province, Changsha 410008.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2025 Jan 28;50(1):99-104. doi: 10.11817/j.issn.1672-7347.2025.240134.

DOI:10.11817/j.issn.1672-7347.2025.240134
PMID:40457795
Abstract

Atypical placental site nodules (APSN) are a rare form of trophoblastic disease in pregnancy. There is limited research on APSN, and treatment methods are controversial, with unclear prognosis. This study collected clinical and prognostic data of 5 patients diagnosed with APSN at Xiangya Hospital of Central South University from June 2008 to June 2023, aiming to provide a better understanding of the prognosis of APSN patients and offer scientific evidence for clinical treatment. The average age of the 5 APSN patients was 32.60 years, and all patients underwent dilation and curettage or hysteroscopic surgery or hysteroscopic surgery without hysterectomy. Except for one patient who was lost to follow-up after 30 days, the remaining 4 patients were followed up for 1.36 to 4.61 years. During the follow-up, gynecological ultrasound did not show abnormalities, and serum human chorionic gonadotropin (HCG) tests were negative, with no evidence of malignancy. A search of both English and Chinese databases yielded 8 articles reporting the diagnosis, treatment, and follow-up outcomes of APSN, with 37 cases cumulatively followed up. Among them, 2 (5.41%) cases developed epithelial trophoblastic tumors or placental site trophoblastic tumors during follow-up, but there is insufficient evidence to determine whether these tumors directly originated from APSN or were secondary to APSN. Currently, there is no direct evidence suggesting that APSN has the potential for malignant transformation. Patients with APSN who have completed their childbearing may consider preserving their uterus, but close follow-up is needed to further evaluate the prognosis.

摘要

非典型胎盘部位结节(APSN)是妊娠期一种罕见的滋养细胞疾病形式。关于APSN的研究有限,治疗方法存在争议,预后尚不清楚。本研究收集了2008年6月至2023年6月在中南大学湘雅医院确诊为APSN的5例患者的临床和预后数据,旨在更好地了解APSN患者的预后,并为临床治疗提供科学依据。5例APSN患者的平均年龄为32.60岁,所有患者均接受了刮宫术或宫腔镜手术或未行子宫切除术的宫腔镜手术。除1例患者在30天后失访外,其余4例患者随访了1.36至4.61年。随访期间,妇科超声未显示异常,血清人绒毛膜促性腺激素(HCG)检测为阴性,无恶性证据。检索英文和中文数据库共获得8篇报道APSN诊断、治疗及随访结果的文章,累计随访37例。其中,2例(5.41%)在随访期间发生上皮样滋养细胞肿瘤或胎盘部位滋养细胞肿瘤,但尚无足够证据确定这些肿瘤是否直接起源于APSN或继发于APSN。目前,没有直接证据表明APSN有恶变潜能。已完成生育的APSN患者可考虑保留子宫,但需要密切随访以进一步评估预后。

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