[1]马晓黎,段华*.青春期生殖道畸形的临床特点与处理原则[J].中国计划生育和妇产科,2020,(3):14-16,20.
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青春期生殖道畸形的临床特点与处理原则
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《中国计划生育和妇产科》[ISSN:1674-4020/CN:51-1708/R]

卷:
期数:
2020年3期
页码:
14-16,20
栏目:
女性生殖器官发育异常诊治专题
出版日期:
2020-03-25

文章信息/Info

作者:
马晓黎段华*
首都医科大学附属北京妇产医院妇科微创中心
关键词:
青春期生殖道畸形临床特点诊治
分类号:
R 7111

参考文献/References:

[1]Trent M, Haggerty C L, Jennings J M, et al.Adverse adolescent reproductive health outcomes after pelvic inflammatory disease [J].Archives of Pediatrics & Adolescent Medicine, 2011, 165(1): 49-54. [2]李清,华克勤.与女性生殖道发育异常相关子宫内膜异位症的诊治策略 [J].实用妇产科杂志,2018,34(9):646-647. [3]朱兰.跟进女性生殖道畸形诊治发展,减少误诊误治 [J].中国实用妇科与产科杂志,2018,34(4):355-356. [4]中华医学会妇产科学分会.女性生殖器官畸形诊治的中国专家共识 [J].中华妇产科杂志,2015,50(10):729-733. [5]Dovey S, Sanfilippo J.Endometriosis and the adolescent[J].Clinical Obstetrics and Gynecology, 2010, 53(2): 420-428. [6]Janssen E B, Rijkers A, Hoppenbrouwers K, et al.Prevalence of endometriosis diagnosed by laparoscopy in adolescents with dysmenorrhea or chronic pelvic pain: a systematic review[J].Human Reproduction Update, 2013, 19(5): 570-582. [7]Matalliotakis M, Goulielmos G N, Matalliotaki C, et al.Endometriosis in adolescent and young girls: report on a series of 55 cases [J].Journal of Pediatric and Adolescent Gynecology, 2017, 30(5): 568-570. [8]Vaughan E D, Middleton G W.Pertinent genitourinary embryology: review for practicing urologist [J].Urology, 1975, 6(2): 139-149. [9]Rall K, Eisenbeis S, Henninger V, et al.Typical and atypical associated findings in a group of 346 patients with Mayer-Rokitansky-Kuester-Hauser syndrome[J].Journal of Pediatric and Adolescent Gynecology, 2015, 28(5): 362-368. [10]Kapczuk K, Iwaniec K, Friebe Z, et al.Congenital malformations and other comorbidities in 125 women with Mayer-Rokitansky-Küster-Hauser syndrome[J].European Journal of Obstetrics & Gynecology and Reproductive Biology, 2016, 207: 45-49. [11]Hall-Craggs M A, Kirkham A, Creighton S M .Renal and urological abnormalities occurring with Mullerian anomalies[J].Journal of Pediatric Urology, 2013, 9(1):27-32. [12]FedeleL, Motta F, Frontino G, et al.Double uterus with obstructed hemivagina and ipsilateral renal agenesis: pelvic anatomic variants in 87 cases [J].Human Reproduction, 2013, 28(6): 1580-1583. [13]Song Xiaochen, Zhu Lan, Ding Jing, et al.Clinical characteristics of congenital cervical atresia and associated endometriosis among 96 patients [J].International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics, 2016, 134(3): 252-255. [14]王欣,段华.先天性处女膜闭锁16例临床分析并文献复习 [J].北京医学,2017,39(4):407-408. [15]中华医学会妇产科学分会.关于阴道斜隔综合征,MRKH综合征和阴道闭锁诊治的中国专家共识 [J].中华妇产科杂志,2018,54(1):35-42. [16]马晓黎,段华.宫腔镜在子宫发育异常诊治中的应用 [J].实用妇产科杂志,2019,35(11):812-815. [17]ACOG Committee on Adolescent Health Care.ACOG committee opinion no.728 summary: müllerian agenesis: diagnosis, management, and treatment [J].Obstetrics and Gynecology, 2018, 131(1): 196-197. [18]马晓黎,段华.ACOG关于MRKH综合征诊治的最新建议 [J].中国实用妇科与产科杂志,2019,35(11):1269-1272. [19]Kriplani A, Kachhawa G, Awasthi D, et al.Laparoscopic-assisted uterovaginal anastomosis in congenital atresia of uterine cervix: follow-up study [J].Journal of Minimally Invasive Gynecology, 2012, 19(4): 477-484. [20]El Saman A M.Endoscopically monitored canalization for treatment of congenital cervical atresia: the least invasive approach[J].Fertility and Sterility, 2010, 94(1): 313-316. [21]马晓黎,段华.子宫发育异常的微创手术矫治 [J].实用妇产科杂志,2018,34(9):643-645.

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备注/Memo

备注/Memo:
北京市医院管理局临床医学发展专项-“扬帆计划”(项目编号:ZYLX201406);首都医科大学临床医学高精尖学科建设项目(项目编号:No.1192070309)
更新日期/Last Update: 2020-03-25