Modern methods of surgical treatment of obstructive genital malformations in girls

封面


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

Congenital anomalies of female genital tract in children and adolescents are more commonly detected at the age of menarche with several symptoms caused by obstruction. These diseases are rare, but without timely diagnostics and management they can cause a number of serious complications. This article is aimed to review modern approaches to diagnostics and management of this pathology and to highlight some aspects that require further research.

A literature search was conducted using the following databases: MEDLINE, Google Scholar, eLIBRARY, international guidelines and clinical recommendations. Key words that were used for search were: «congenital malformations», «distal vaginal atresia», «imperforated hymen», «OHVIRA», «transverse vaginal septum», «hematocolpos», «obstructive uterovaginal anomalies», «surgical treatment in pediatrics». International clinical trials which had been analysed by the authors were included in the review.

They have explored the current literature related to the following obstructive malformations: distal vaginal atresia, transverse vaginal septum, imperforated hymen and Herlin–Werner–Wunderlich syndrome.

Main conclusions are: further studies with a larger sample of patients, longer follow-up, long-term outcomes and effective preventive measures against complications. Another unresolved question is the age which can be recommended for surgical treatment of obstructive malformations. Potentials for developing new algorithms of earlier diagnostics are also among research priorities.

全文:

受限制的访问

作者简介

Leila Adamyan

Research Center for Obstetrics, Gynecology and Perinatology; Russian University of Medicine

Email: endogyn@yandex.ru
ORCID iD: 0000-0002-3253-4512
SPIN 代码: 9836-2713

MD, Dr. Sci. (Medicine), Professor, Academician of the Russian Academy of Sciences

俄罗斯联邦, Moscow; Moscow

Elena Sibirskaya

Research Center for Obstetrics, Gynecology and Perinatology; Russian Children's Clinical Hospital; The Russian National Research Medical University named after N.I. Pirogov

Email: elsibirskaya@yandex.ru
ORCID iD: 0000-0002-4540-6341
SPIN 代码: 1356-9252

MD, Dr. Sci. (Medicine), Professor

俄罗斯联邦, Moscow; Moscow; Moscow

Sergey Sharkov

Morozov Children's Municipal Clinical Hospital; I.M. Sechenov First Moscow State Medical University (Sechenov University)

Email: sharkdoc@mail.ru
ORCID iD: 0000-0001-8579-2227
SPIN 代码: 4637-6392

MD, Dr. Sci. (Medicine), Professor

俄罗斯联邦, Moscow; Moscow

Laura Pivazyan

Research Center for Obstetrics, Gynecology and Perinatology

Email: laurapivazyan98@gmail.com
ORCID iD: 0000-0002-6844-3321
SPIN 代码: 3949-2120

MD

俄罗斯联邦, Moscow

Kamila Murvatova

S.P. Botkin City Clinical Hospital

编辑信件的主要联系方式.
Email: murvatovakamila@gmail.com
ORCID iD: 0000-0002-3245-6948

MD

Moscow

Evdokiya Zarova

I.M. Sechenov First Moscow State Medical University (Sechenov University)

Email: zarovaea@mail.ru
ORCID iD: 0000-0003-4693-6886
俄罗斯联邦, Moscow

参考

  1. Grimbizis GF, Gordts S, Di Spiezio Sardo A, et al. The ESHRE/ESGE consensus on the classification of female genital tract congenital anomalies. Human Rep (Oxford, England). 2013;28(8):2032–2044. doi: 10.1093/humrep/det098
  2. Ludwin A, Ludwin I. Comparison of the ESHRE-ESGE and ASRM classifications of Müllerian duct anomalies in everyday practice. Human Rep (Oxford, England). 2015;30(3):569–580. doi: 10.1093/humrep/deu344
  3. Acién P, Acién MI. The history of female genital tract malformation classifications and proposal of an updated system. Human Rep Update. 2011;17(5):693–705. doi: 10.1093/humupd/dmr021
  4. Adamyan LV, Kuznetsova MV, Popryaduhin AY, et al. Genetic aspects of malformations of female genital organs: A modern view of the problem. Russ J Human Rep. 2023;29(4-2):23–28. EDN: JXBBWH doi: 10.17116/repro20232904223
  5. Maciel C, Bharwani N, Kubik-Huch RA, et al. MRI of female genital tract congenital anomalies: European Society of Urogenital Radiology (ESUR) guidelines. Eur Radiol. 2020;30(8):4272–4283. EDN: NTWYEB doi: 10.1007/s00330-020-06750-8
  6. Management of Acute Obstructive Uterovaginal Anomalies: ACOG Committee Opinion, Number 779. Obstetrics and gynecology. 2019;133(6):e363–e371. doi: 10.1097/AOG.0000000000003281
  7. Akhtar MA, Saravelos SH, Li TC, Jayaprakasan K. Royal College of Obstetricians and Gynaecologists. Reproductive implications and management of congenital uterine anomalies: Scientific impact paper No. 62 November 2019. BJOG. 2020;127(5):e1–e13. doi: 10.1111/1471-0528.15968
  8. Valle RF, Ekpo GE. Hysteroscopic metroplasty for the septate uterus: Review and meta-analysis. J Minimally Invasive Gynecol. 2013;20(1):22–42. doi: 10.1016/j.jmig.2012.09.010
  9. Chandler TM, Machan LS, Cooperberg PL, et al. Mullerian duct anomalies: From diagnosis to intervention. Brit J Radiol. 2009;82(984):1034–1042. doi: 10.1259/bjr/99354802
  10. Tanitame K, Tanitame N, Urayama S, et al. Congenital anomalies causing hemato/hydrocolpos: Imaging findings, treatments, and outcomes. Jpn J Radiol. 2021;39(8):733–740. EDN: NCSPIY doi: 10.1007/s11604-021-01115-7
  11. Michala L, Aslam N, Conway GS, Creighton SM. The clandestine uterus: Or how the uterus escapes detection prior to puberty. BJOG. 2010;117(2):212–215. doi: 10.1111/j.1471-0528.2009.02413.x
  12. Kresowik J, Ryan GL, Austin JC, van Voorhis BJ. Ultrasound-assisted repair of a unique case of distal vaginal agenesis. Fertility Sterility. 2007;87(4):976.e9–976.e9.76E12. EDN: LTFPRH doi: 10.1016/j.fertnstert.2006.06.062
  13. Adair L, Georgiades M, Osborne R, Ng T. Uterus didelphys with unilateral distal vaginal agenesis and ipsilateral renal agenesis: Common presentation of an unusual variation. J Radiol Case Reports. 2011;5(1):1–8. doi: 10.3941/jrcr.v5i1.572
  14. Eksioglu AS, Maden HA, Cinar G, Yildiz TY. Imperforate hymen causing bilateral hydroureteronephrosis in an infant with bicornuate uterus. Case Rep Urol. 2012;2012:102683.
  15. Bischoff A, Alaniz VI, Trecartin A, Peña A. Vaginal reconstruction for distal vaginal atresia without anorectal malformation: Is the approach different? Pediatr Surg Int. 2019;35(9):963–966. EDN: VFDEFF doi: 10.1007/s00383-019-04512-2
  16. Ugur MG, Balat O, Ozturk E, et al. Pitfalls in diagnosis and management of distal vaginal agenesis: 10-year experience at a single centre. Eur J Obstet Gynecol Reprod Biol. 2012;163(1):85–90. doi: 10.1016/j.ejogrb.2012.03.024
  17. Dural O, Ugurlucan FG, Yasa C, et al. A case of distal vaginal agenesis presenting with recurrent urinary tract infection and pyuria in a prepubertal girl. J Pediatr Adolesc Gynecol. 2017;30(1):e7–e10. doi: 10.1016/j.jpag.2016.08.007
  18. Priyatini T, Moegni F, Hidayah GN, et al. Case series: Interdigitating "Y" flap for transverse vaginal septum management. Int J Surg Case Rep. 2022;(100):107601. doi: 10.1016/j.ijscr.2022.107601
  19. Bobkova MV, Puchko TK, Adamyan LV. Reproduction in women with congenital uterus and vagina anomalies. Russ J Human Rep. 2018;24(2):42–53. EDN: XPLZFJ doi: 10.17116/repro201824242-53
  20. Williams CE, Nakhal RS, Hall-Craggs MA, et al. Transverse vaginal septae: Management and long-term outcomes. BJOG. 2014;121(13):1653–1658. doi: 10.1111/1471-0528.12899
  21. Singh S, Biswas M, Dey M, et al. A rare case of low transverse vaginal septum. Int J Reprod Contracept Obstet Gynecol. 2015;4(6):2103–2106.
  22. Abdelrahman HM, Feloney MP. Imperforate hymen. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2022.
  23. Lee KH, Hong JS, Jung HJ, et al. Imperforate hymen: A comprehensive systematic review. J Clin Med. 2019;8(1):56. doi: 10.3390/jcm8010056
  24. Batyrova ZK, Uvarova EV, Kumykova ZK, et al. Congenital disorders of genital organs with menstrual blood outflow defect: Diagnostics, treatment and prevention of complications. Pediatric Pharmacol. 2019;16(6):349–352. EDN: XZIZZU doi: 10.15690/pf.v16i6.2072
  25. Cetin C, Soysal C, Khatib G, et al. Annular hymenotomy for imperforate hymen. J Obstet Gynaecol Res. 2016;42(8):1013–1015. doi: 10.1111/jog.13010
  26. Acar A, Balci O, Karatayli R, et al. The treatment of 65 women with imperforate hymen by a central incision and application of Foley catheter. BJOG. 2007;114(11):1376–1379. doi: 10.1111/j.1471-0528.2007.01446.x
  27. Parker PB, Edwards JR, Bochnakova TN, Lee DM. Image-guided transvaginal and transabdominal drain placement for surgical navigation in a patient with tubo-ovarian abscess and obstructed hemivagina and ipsilateral renal anomaly syndrome. J Pediatr Adolesc Gynecol. 2022;35(1):94–97. EDN: UEIYTI doi: 10.1016/j.jpag.2021.07.006
  28. Kudela G, Wiernik A, Drosdzol-Cop A, et al. Multiple variants of obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome: One clinical center case series and the systematic review of 734 cases. J Pediatr Urol. 2021;17(5):653.e1–653.e9. doi: 10.1016/j.jpurol.2021.06.023
  29. Arakelyan AS, Gus AI, Adamyan LV, et al. The role of 3d echographic diagnostics in the choice of tactics for reconstructive plastic surgery in case of abnormalities of the development of the uterus and vagina. Russ J Human Reproduct. 2021;27(4):32–42. EDN: TCIGLZ doi: 10.17116/repro20212704132
  30. Kriplani A, Dalal V, Kachhawa G, et al. Minimally invasive endoscopic approach for management of OHVIRA syndrome. J Obstet Gynaecol India. 2019;69(4):350–355. EDN: PKWBRG doi: 10.1007/s13224-019-01240-4
  31. Akhapkina ES, Batyrova ZK, Сhuprynin VD, et al. Features of the management of girls with anomalies of the genitourinary system. Gynecology. 2021;23(3):245–249. EDN: UTYBOS doi: 10.26442/20795696.2021.3.200951
  32. Cheng C, Subedi J, Zhang A, et al. Vaginoscopic incision of oblique vaginal septum in adolescents with OHVIRA syndrome. Sci Rep. 2019;9(1):20042. doi: 10.1038/s41598-019-56471-2
  33. Ludwin A, Ludwin I, Bhagavath B, et al. Virginity-sparing management of blind hemivagina in obstructed hemivagina and ipsilateral renal anomaly syndrome. Fertil Steril. 2018;110(5):976–978. doi: 10.1016/j.fertnstert.2018.07.007

补充文件

附件文件
动作
1. JATS XML

版权所有 © Eco-Vector, 2024

##common.cookie##