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先天性宫颈阴道发育不全合并功能性子宫:一例病例报告及文献复习

Congenital cervico-vaginal aplasia with a functional uterus: A case report and review of literature.

作者信息

Faraj Chaymae, Essetti Sara, Bahlouli Nourrelhouda, Chait Fatima, Allali Nazik, Chat Latifa, El Haddad Siham

机构信息

Gynecology Radiology Department, Maternity Hospital, Ibn Sina Hospital, Mohamed V University, Rabat, Morocco.

出版信息

SAGE Open Med Case Rep. 2024 Jun 10;12:2050313X241260217. doi: 10.1177/2050313X241260217. eCollection 2024.

DOI:10.1177/2050313X241260217
PMID:38864032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11165953/
Abstract

Maldevelopment of the vagina and cervix is frequently accompanied by uterine aplasia or hypoplasia. Complete cervico-vaginal aplasia with a normally developing uterus is a very uncommon type of developmental failure. Failure to treat the condition can result in complications such as hematometra and hematosalpinx caused by the retrograde flow of blood into the fallopian tubes. In this case report, we describe the case of a 32-year-old woman experiencing cyclic abdominal pain and primary amenorrhea. The patient exhibited cervico-vaginal agenesis, with a functional uterus that was complicated by hematometra and bilateral hematosalpinx.

摘要

阴道和宫颈发育异常常伴有子宫发育不全或发育不良。子宫发育正常但宫颈阴道完全发育不全是一种非常罕见的发育障碍类型。不治疗这种疾病可能会导致诸如血液逆流至输卵管引起的子宫积血和输卵管积血等并发症。在本病例报告中,我们描述了一名32岁女性,她经历周期性腹痛和原发性闭经。患者表现为宫颈阴道发育不全,功能性子宫伴有子宫积血和双侧输卵管积血。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acfa/11165953/e7c73f516140/10.1177_2050313X241260217-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acfa/11165953/e140f7e30302/10.1177_2050313X241260217-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acfa/11165953/e7c73f516140/10.1177_2050313X241260217-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acfa/11165953/e140f7e30302/10.1177_2050313X241260217-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acfa/11165953/e7c73f516140/10.1177_2050313X241260217-fig2.jpg

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本文引用的文献

1
The Path of Birth is Not Always Normal: A Case Report of Cervicovaginal Agenesis.出生途径并非总是正常:宫颈阴道发育不全病例报告
Gynecol Minim Invasive Ther. 2021 Nov 5;10(4):247-251. doi: 10.4103/GMIT.GMIT_57_20. eCollection 2021 Oct-Dec.
2
Secondary pyosalpinx after reconstructive surgery of vaginal agenesis patient with bilateral hematosalpinx: A case report.阴道闭锁患者双侧输卵管积血重建手术后继发输卵管积脓:一例报告
Int J Surg Case Rep. 2021 Aug;85:106166. doi: 10.1016/j.ijscr.2021.106166. Epub 2021 Jul 2.
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先天性宫颈阴道发育不全的腹腔镜治疗
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Imperforate hymen and ruptured hematosalpinx: a case report with a review of the literature.处女膜闭锁与输卵管积血破裂:一例病例报告并文献复习
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The clinical management of congenital absence of the uterine cervix.
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