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双子宫伴阴道横隔——一种复杂罕见的苗勒管畸形

Uterine Didelphys with Transverse Vaginal Septum - A Complex Rare Müllerian Anomaly.

作者信息

Khan Dina Aisha, Sharma Nalini, Saha Anusmita, Das Rituparna, Panda Subrat

机构信息

Department of Obstetrics and Gynaecology, Hamdard Institute of medical sciences and research, New Delhi, India.

Department of Obstetrics and Gynaecology, North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences, Shillong, Meghalaya, India https://orcid.org/ID-0000-0001-5462-3017.

出版信息

Acta Med Litu. 2021;28(2):367-373. doi: 10.15388/Amed.2021.28.2.2. Epub 2021 Jul 29.

DOI:10.15388/Amed.2021.28.2.2
PMID:35474935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8958649/
Abstract

During the development of the female genital tract, any insult to the normal development process results in a set of intriguing abnormalities known as Müllerian duct abnormalities. The uterine didelphys is the second least common type of anomaly among these, which may commonly be associated with a longitudinal vaginal septum (lateral fusion defect). However uterine didelphys along with a transverse vaginal septum (lateral fusion plus resorption defect) is a very rare finding and to the best of our knowledge, thecase that we hereby report is the second one in literature. A 16-year-old unmarried girl presented with primary amenorrhoea and cyclical pain for 18months.On clinical examination and imaging, a case of uterine didelphys and transverse vaginal septum was found. Her urinary tract was normalon USG and MRI evaluation. Excision of the septum was done by abdomino-vaginal approach. The patient was discharged well. We conclude that a patient presenting with primary amenorrhea especially with cyclical dysmenorrhea with a transverse vaginal septum on examination should be thoroughly investigated for associated upper genital tract abnormalities as the treatment strategy and prognosis is largely dependent on the correct classification of the anomaly.

摘要

在女性生殖道发育过程中,任何对正常发育过程的损害都会导致一系列有趣的异常情况,即苗勒管异常。双子宫是其中第二少见的异常类型,通常可能与纵向阴道纵隔(侧方融合缺陷)相关。然而,双子宫合并横向阴道纵隔(侧方融合加吸收缺陷)是一种非常罕见的情况,据我们所知,我们在此报告的病例是文献中的第二例。一名16岁未婚女孩因原发性闭经和周期性疼痛18个月前来就诊。经临床检查和影像学检查,发现为双子宫和横向阴道纵隔病例。超声检查和磁共振成像评估显示她的泌尿系统正常。通过腹-阴道联合途径切除纵隔。患者康复出院。我们得出结论,对于出现原发性闭经尤其是伴有周期性痛经且检查发现有横向阴道纵隔的患者,应全面检查是否存在相关的上生殖道异常,因为治疗策略和预后在很大程度上取决于对异常情况的正确分类。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8958649/ed2b98a5ee35/aml-28-367-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8958649/e9a4c53a9030/aml-28-367-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8958649/b26dc9cdb48c/aml-28-367-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8958649/684f20f92c75/aml-28-367-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8958649/ed2b98a5ee35/aml-28-367-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8958649/e9a4c53a9030/aml-28-367-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8958649/b26dc9cdb48c/aml-28-367-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8958649/684f20f92c75/aml-28-367-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f39/8958649/ed2b98a5ee35/aml-28-367-g004.jpg

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本文引用的文献

1
Obstructive Müllerian Anomalies in Menstruating Adolescent Girls: A Report of 22 Cases.青春期有月经的女孩中的梗阻性苗勒管异常:22例报告
J Pediatr Adolesc Gynecol. 2018 Jun;31(3):252-257. doi: 10.1016/j.jpag.2017.09.013. Epub 2017 Oct 10.
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Didelphys Uterus: A Case Report and Review of the Literature.双子宫:一例病例报告及文献综述
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Rare Müllerian Anomaly: Complete Septate Uterus with Simultaneous Longitudinal and Transverse Vaginal Septa.
罕见的苗勒管异常:完全纵隔子宫合并阴道纵膈与横膈
J Pediatr Adolesc Gynecol. 2015 Dec;28(6):e189-91. doi: 10.1016/j.jpag.2015.04.012. Epub 2015 May 9.
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Imaging Diagnosis of Herlyn-Werner-Wunderlich Syndrome- An Extremely Rare Urogenital Anomaly.赫林-韦纳-温德利希综合征的影像学诊断——一种极其罕见的泌尿生殖系统异常
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Treatment of patients with a congenital transversal vaginal septum or a partial aplasia of the vagina. The vaginal pull-through versus the push-through technique.先天性横向阴道隔或部分阴道发育不全患者的治疗。阴道拖出术与推进术。
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