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稽留流产后继发宫颈葡萄胎伴严重阴道出血 1 例:病例报告及文献复习

Cervical hydatidiform mole pregnancy after missed abortion presenting with severe vaginal bleeding: case report and review of the literature.

机构信息

Department of Gynecology and Obstetrics, University Hospital Ulm, Prittwitzstraße 43, 89075 Ulm, Germany.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2011 May;156(1):9-11. doi: 10.1016/j.ejogrb.2010.12.029. Epub 2011 Jan 26.

Abstract

We report a 28-year-old woman presenting with a complete hyaditiform mole localized to the cervix. She had undergone curettage of missed abortion two months previously and the aborted material showed normal placental tissue on histopathologic examination. Two months after curettage she presented with sudden severe vaginal bleeding. Clinical examination revealed a lesion of the epithelial outer surface of the cervix. Due to the bleeding, immediate surgical intervention was necessary. Histological examination revealed a complete hydatidiform mole. Currently, only three cases of this exceedingly rare diagnosis have been published: two reported a partial mole and one a complete hydatidiform mole. In our case, we hypothesize that the pathogenesis took place in two steps. Initially the curettage of the missed abortion damaged the endometrial lining. During a new rapid re-fertilization after the missed abortion, a hydatidiform molar pregnancy developed. Normally this abnormal trophoblast tissue would adhere to the endometrium but in this case we assume that intrauterine implantation was not possible because of endometrial damage at the prior curettage, allowing the abnormal trophoblast tissue to pass the endocervix and emerge into the vaginal vault. Presumably, during the curettage an epithelial defect was produced on the outer surface of the cervix, due to clamping the cervix during dilatation. We speculate that this weak spot on the epithelial surface was responsible for the adherence to the cervix and subsequent bleeding was caused by injury of maternal blood vessels. We propose that careful holding of the cervix with atraumatic clamps during curettage is important to avoid subsequent complications.

摘要

我们报告了一例 28 岁女性,表现为完全性葡萄胎局限于宫颈。两个月前她因稽留流产而行刮宫术,流产组织的组织病理学检查显示正常胎盘组织。刮宫术后两个月,她突然出现严重阴道出血。临床检查发现宫颈上皮外表面有病变。由于出血,需要立即进行手术干预。组织学检查显示完全性葡萄胎。目前,仅发表了三例这种极其罕见的诊断病例:两例报告部分性葡萄胎,一例报告完全性葡萄胎。在我们的病例中,我们假设发病机制分两步发生。首先,稽留流产的刮宫术损伤了子宫内膜。在稽留流产后新的快速再受精时,发生了葡萄胎妊娠。正常情况下,这种异常滋养细胞组织会附着在子宫内膜上,但在这种情况下,我们假设由于先前刮宫术导致的子宫内膜损伤,宫内植入不可能发生,允许异常滋养细胞组织通过宫颈内口并进入阴道穹窿。推测在刮宫术时,由于宫颈扩张时夹闭宫颈,导致宫颈外表面出现上皮缺损。我们推测,上皮表面的这个薄弱点负责与宫颈黏附,随后的出血是由于母体血管损伤引起的。我们建议在刮宫术时用无创伤的宫颈钳小心握持宫颈,以避免随后发生并发症。

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