WANG LieHong. One case of congenital no cervix, no vaginal, bilateral chocolate cysts with MRKH syndrome (type II). 2025. biomedRxiv.202501.00072
One case of congenital no cervix, no vaginal, bilateral chocolate cysts with MRKH syndrome (type II)
Corresponding author: WANG LieHong, doctorwifi@126.com
DOI: 10.12201/bmr.202501.00072
-
Abstract: In the clinical work of obstetrics and gynecology,congenital absence of cervix,absence of vagina,bilateral chocolate cyst with MRKH syndrome (type II) is an extremely rare congenital dysmorphic disease of the reproductive system,which is typically manifested by dysplasia or absence of uterus and vagina.Patients with MRKH syndrome type II often have ovarian lesions (eg,bilateral chocolate cysts) and other systemic abnormalities (eg,urinary or skeletal dysplasia) in addition to genital tract abnormalities.This article describes the treatment of a patient with congenital cervical,nonvaginal,bilateral chocolate cyst and MRKH syndrome (type II).The patient,a 17-year-old female,was admitted to the hospital complaining of menstrual cramps and lower abdominal pain for 2 days.Gynecologic examination reveals vulva:poorly developed pubic hair,poorly developed labia minora,small hymen orifice,visible separation in the middle,and cotton swabs unable to penetrate.Pelvic MRI was performed immediately afterwards,and the results showed endometrial thickening,cervical dysplasia,no visible in the lower one-third of the vagina,and no development of the caudal vertebrae.Combined with the results of the patients auxiliary examination, under the discussion of the department director and all doctors,and with the consent of the patients family,it is planned to decide to undergo laparoscopic vaginoplasty (acellular allodermis) + cervicopy + hysteroscopy + laparoscopic bilateral ovarian cystectomy + ultrasound-guided uterine balloon placement.After careful care after the operation,the results of the re-examination of B-ultrasound improved significantly,and the patient was successfully discharged from the hospital.
Key words: MRKH syndrome; chocolate cyst; congenital malformation of the female genital tract; vaginoplasty.Submit time: 23 January 2025
Copyright: The copyright holder for this preprint is the author/funder, who has granted biomedRxiv a license to display the preprint in perpetuity. -
图表
-
zhangming. One case of unicornuate uterus with residual horn uterus and right kidney absence complicated with ovarian endometriotic cyst. 2025. doi: 10.12201/bmr.202504.00055
LUAN Zhi-Yong. Research progress of stem cell therapy for Hirschsprung disease. 2024. doi: 10.12201/bmr.202410.00021
Chen Xin Yan, Guo Fang, Li Wei, Chen Hai Tang. Efficacy of the single-port laparoscopic technique in the treatment of ovarian cysts. 2024. doi: 10.12201/bmr.202410.00071
YU Shifang. A case of passenger lymphocyte syndrome in a lung transplant patient with minor ABO-incompatible and a discussion of the transfusion strategy. 2025. doi: 10.12201/bmr.202504.00002
邝文健, Zheng Tuo, Dai Lingai, Zhou Tingjun, Luo Sheng. Mounier-Kuhn syndrome: report of two cases and literature review. 2025. doi: 10.12201/bmr.202504.00057
wangazhen, lixinag, shijingyu, yetao, wuyuanhua. Gillan - the barre syndrome complicated by myasthenia gravis in 1 case. 2024. doi: 10.12201/bmr.202408.00038
shenyanqun, zhanglulu. Analysis on clinical features and prognostic factors in 68 adult hemophagocytic syndrome. 2025. doi: 10.12201/bmr.202502.00008
XuHong. Advances in the treatment of osteopenia-seropathic obesity syndrome in the elderly. 2024. doi: 10.12201/bmr.202411.00064
文军. Treatment of left maxillary central incisor with root canal calcification and lateral cyst: a case report. 2024. doi: 10.12201/bmr.202412.00065
Zhang zhenwen. Effects of SGLT2 inhibitors on the metabolic syndrome and its components. 2025. doi: 10.12201/bmr.202503.00002
-
ID Submit time Number Download 1 2025-01-05 bmr.202501.00072V1
Download -
-
Public Anonymous To author only
Get Citation
Article Metrics
- Read: 88
- Download: 2
- Comment: 0