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摘要: 阴道斜隔综合征(oblique vaginal septum syndrome,OVSS)是少见的女性泌尿生殖系统畸形,临床表现复杂多样,易漏诊、误诊。超声可对该病变进行全面、客观评估,是诊断OVSS的首选影像学方法。本文主要对超声检查技术在OVSS诊断中的应用价值进行综述。Abstract: Oblique vaginal septum syndrome (OVSS) is a rare malformation of the female urogenital system. Its clinical manifestations are complex and diverse. It is easy for physicians to misdiagnose or fail to diagnose OVSS. Ultrasound can make a comprehensive and objective assessment of the lesion, which is the preferred imaging method for the diagnosis of OVSS. This article mainly reviews the application value of ultrasonographic technology in the diagnosis of OVSS.作者贡献:张新梅查阅文献,撰写论文;夏宇指导论文写作方向,审阅并修改论文;姜玉新参与论文指导。利益冲突 无
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[1] Fedele L, Motta F, Frontino G, et al. Double uterus with obstructed hemivagina and ipsilateral renal agenesis: pelvic anatomic variants in 87 cases[J]. Hum Reprod, 2013, 28: 1580-1583. doi: 10.1093/humrep/det081 [2] Zhang H, Ning G, Fu C, et al. Herlyn-Werner-Wunderlich syndrome: diverse presentations and diagnosis on MRI[J]. Clin Radiol, 2020, 75: 480. e17-480. e25. doi: 10.1016/j.crad.2020.01.016 [3] Piccinini PS, Doski J. Herlyn-Werner-Wunderlich syndrome: a case report[J]. Rev Bras Ginecol Obstet, 2015, 37: 192-196. doi: 10.1590/SO100-720320150005077 [4] 卞美璐, 黄荣丽, 吴葆桢, 等. 先天性阴道斜隔[J]. 中华妇产科杂志, 1985, 20: 85-88. https://www.cnki.com.cn/Article/CJFDTOTAL-GWVC201103025.htm [5] Burgis J. Obstructive Müllerian anomalies: case report, diagnosis, and management[J]. Am J Obstet Gynecol, 2001, 185: 338-344. doi: 10.1067/mob.2001.116738 [6] Vercellini P, Daguati R, Somigliana E, et al. Asymmetric lateral distribution of obstructed hemivagina and renal agenesis in women with uterus didelphys: institutional case series and a systematic literature review[J]. Fertil Steril, 2007, 87: 719-724. doi: 10.1016/j.fertnstert.2007.01.173 [7] Zurawin RK, Dietrich JE, Heard MJ, et al. Didelphic uterus and obstructed hemivagina with renal agenesis: case report and review of the literature[J]. J Pediatr Adolesc Gynecol, 2004, 17: 137-141. doi: 10.1016/j.jpag.2004.01.016 [8] Prada Arias M, Muguerza Vellibre R, Montero Sánchez M, et al. Uterus didelphys with obstructed hemivagina and multicystic dysplastic kidney[J]. Eur J Pediatr Surg, 2005, 15: 441-445. doi: 10.1055/s-2005-872926 [9] Zhu L, Chen N, Tong JL, et al. New classification of Herlyn-Werner-Wunderlich syndrome[J]. Chin Med J (Engl), 2015, 128: 222-225. doi: 10.4103/0366-6999.149208 [10] 陈娜, 朱兰, 蒋宇林, 等. 一种特殊类型的阴道斜隔综合征一例[J]. 中华妇产科杂志, 2011, 46: 396. doi: 10.3760/cma.j.issn.0529-567x.2011.05.022 [11] Khaladkar SM, Kamal V, Kamal A, et al. The Herlyn-Werner-Wunderlich Syndrome-A Case Report with Radiological Review[J]. Pol J Radiol, 2016, 81: 395-400. doi: 10.12659/PJR.897228 [12] Kumar S, Rajagopal KV, Karegowda LH, et al. Herlyn-Werner-Wunderlich syndrome: a rare cause of acute urinary retention in an adolescent girl[J]. BMJ Case Rep, 2015, 2015: bcr2015209638. doi: 10.1136/bcr-2015-209638 [13] Wu TH, Wu TT, Ng YY, et al. Herlyn-Werner-Wunderlich syndrome consisting of uterine didelphys, obstructed hemivagina and ipsilateral renal agenesis in a newborn[J]. Pediatr Neonatol, 2012, 53: 68-71. doi: 10.1016/j.pedneo.2011.11.014 [14] Sanghvi Y, Shastri P, Mane SB, et al. Prepubertal presentation of Herlyn-Werner-Wunderlich syndrome: a case report[J]. J Pediatr Surg, 2011, 46: 1277-1280. doi: 10.1016/j.jpedsurg.2011.02.067 [15] 宋泽南, 唐达星, 吴德华, 等. 小儿阴道斜隔综合征临床特点分析[J]. 中华小儿外科杂志, 2019, 40: 456-459. doi: 10.3760/cma.j.issn.0253-3006.2019.05.015 [16] Cappello S, Piccolo E, Cucinelli F, et al. Successful preterm pregnancy in a rare variation of Herlyn-Werner-Wunderlich syndrome: a case report[J]. BMC Pregnancy Childbirth, 2018, 18: 498. doi: 10.1186/s12884-018-2133-2 [17] Li Z, Yu X, Shen J, et al. Scoliosis in Herlyn-Werner-Wunderlich syndrome: a case report and literature review[J]. Medicine (Baltimore), 2014, 93: e185. doi: 10.1097/MD.0000000000000185 [18] Watanabe Y, Etoh T, Nakai H. Adenocarcinoma of the lower female genital tract in patients with Herlyn-Werner-Wunderlich syndrome[J]. Am J Obstet Gynecol, 2012, 207: e5-e6. doi: 10.1016/j.ajog.2012.09.009 [19] Cordoba A, Escande A, Comte P, et al. Locally advanced adenocarcinoma of the cervix on uterus didelphys: a case report[J]. J Contemp Brachytherapy, 2017, 9: 71-76. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346605/ [20] Unal E, Tanyildiz HG, Sonmezer M, et al. Herlyn-Werner-Wunderlich Syndrome: A Rare Cause of Pelvic Pain and High CA 19-9 Levels in an Adolescent Girl[J]. APSP J Case Rep, 2016, 7: 4. http://europepmc.org/articles/PMC4715886 [21] Del Vescovo R, Battisti S, Di Paola V, et al. Herlyn-Werner-Wunderlich syndrome: MRI findings, radiological guide (two cases and literature review), and differential diagnosis[J]. BMC Med Imaging, 2012, 12: 4. doi: 10.1186/1471-2342-12-4 [22] 王绍波, 季云海, 高文涛, 等. 阴道斜隔综合征的CT征像分析[J]. 中国现代医学杂志, 2018, 28: 122-125. https://www.cnki.com.cn/Article/CJFDTOTAL-ZXDY201822027.htm [23] Lee S, Ryu KJ, Ahn KH, et al. Three-dimensional com-puted tomography as a novel method for the diagnosis and management of obstructed hemivagina and ipsilateral renal anomaly syndrome: A case report[J]. J Obstet Gynaecol, 2017, 37: 390-391. doi: 10.1080/01443615.2016.1239072 [24] Yilmaz S, Yildiz AE, Fitoz S. Herlyn-Werner-Wunderlich Syndrome: Sonographic and Magnetic Resonance (MR) Imaging Findings of This Rare Urogenital Anomaly[J]. Pol J Radiol, 2017, 82: 216-219. doi: 10.12659/PJR.899889 [25] Tong J, Zhu L, Lang J. Clinical characteristics of 70 patients with Herlyn-Werner-Wunderlich syndrome[J]. Int J Gynaecol Obstet, 2013, 121: 173-175. doi: 10.1016/j.ijgo.2012.11.023 [26] Schutt AK, Barrett MR, Trotta BM, et al. Perioperative evaluation in Herlyn-Werner-Wunderlich syndrome[J]. Obstet Gynecol, 2012, 120: 948-951. doi: 10.1097/AOG.0b013e318265e35a [27] 马菁苒, 朱兰. 先天性子宫畸形的分类、诊断及类型鉴别[J]. 协和医学杂志, 2014, 5: 455-459. doi: 10.3969/j.issn.1674-9081.2014.04.021 [28] 姚彩, 王继伟, 刘燕娜. 自由解剖平面联合容积对比成像的概述及应用[J]. 中华医学超声杂志(电子版), 2018, 15: 644-648. doi: 10.3877/cma.j.issn.1672-6448.2018.09.002 [29] Grigore M, Pristavu A, Iordache F, et al. Comparative Study of Hysteroscopy and 3D Ultrasound for Diagnosing Uterine Cavity Abnormalities[J]. Rev Med Chir Soc Med Nat Iasi, 2016, 120: 866-873. http://www.ncbi.nlm.nih.gov/pubmed/30141843 [30] Grimbizis GF, Di Spiezio Sardo A, Saravelos SH, et al. The Thessaloniki ESHRE/ESGE consensus on diagnosis of female genital anomalies[J]. Gynecol Surg, 2016, 13: 1-16. http://europepmc.org/abstract/MED/26537921 [31] 王宇, 吕金津, 刘敏, 等. 经腹联合腔内三维超声对阴道斜隔综合征的诊断价值[J]. 中国妇产科临床杂志, 2016, 17: 309-312. https://www.cnki.com.cn/Article/CJFDTOTAL-FKLC201604007.htm [32] 王睿婕, 董秀娟, 宋蕾. 经会阴超声联合腔内容积超声诊断先天性子宫及阴道畸形的价值[J]. 中国医药科学, 2020, 10: 182-186. https://www.cnki.com.cn/Article/CJFDTOTAL-GYKX202015059.htm [33] Khong TL, Siddiqui J, Mallinson P, et al. Herlyn-Werner-Wunderlich syndrome: uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis-role of sonographically guided minimally invasive vaginal surgery[J]. Eur J Pediatr Surg, 2012, 22: 171-173. doi: 10.1055/s-0031-1286341 [34] 王若轶, 邹凌霄, 黄欢, 等. 无损伤处女膜宫腔镜手术治疗阴道斜隔综合征——附13例病例研究[J]. 中国实用妇科与产科杂志, 2018, 34: 89-93. https://www.cnki.com.cn/Article/CJFDTOTAL-ZGSF201801026.htm [35] Han BH, Park SB, Lee YJ, et al. Uterus didelphys with blind hemivagina and ipsilateral renal agenesis (Herlyn-Werner-Wunderlich syndrome) suspected on the presence of hydrocolpos on prenatal sonography[J]. J Clin Ultrasound, 2013, 41: 380-382. doi: 10.1002/jcu.21950 [36] 胡培, 董正森, 郑光美, 等. 超声诊断新生儿期阴道斜隔综合征1例[J]. 中华超声影像学杂志, 2020, 29: 1001-1002. doi: 10.3760/cma.j.cn131148-20200505-00372 [37] Gassner I, Geley TE. Ultrasound of female genital anomalies[J]. Eur Radiol, 2004, 14: L107-L122. doi: 10.1007/s00330-003-2036-z
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