Transverse vaginal septum in a teenager with a history of imperforate hymen: A case report

Lifa Lee, Mariko Matsuno, Sachino Kira, Sotaro Hayashi, Satoshi Nishiyama, Hiroshi Tsujioka
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Abstract

Introduction

Imperforate hymen and transverse vaginal septum are conditions characterized by obstructive defects, typically leading to hematometrocolpos detected around the time of puberty. We encountered a patient who had undergone hymenotomy in infancy to treat pyocolpos due to an imperforate hymen and later developed hematometrocolpos in puberty due to a transverse vaginal septum.

Case presentation

A 13-year-old female presented with hypomenorrhea and hematometrocolpos-induced dysmenorrhea. She had a history of pyocolpos with a urinary tract infection at 3 months of age. At that time, no vaginal opening was found on perineal examination, and imperforate hymen was diagnosed. When hymenotomy was performed, the external cervical os was not detected by intravaginal bronchoscopic examination. However, this abnormal finding was not fully investigated. The postoperative course after hymenotomy was free of complications, and the patient remained asymptomatic until menarche. When she presented 3 months after menarche, genital examination revealed a bulging transverse septum inside the vagina, 5 cm from the hymen. Ultrasound and magnetic resonance imaging revealed a distended uterus, distended upper vagina, and collapsed lower vagina. Transverse vaginal septum was considered, and vaginoscopy was performed to exclude vaginal reclosure or adhesion caused by the previous surgery. A diagnosis of transverse vaginal septum was confirmed, and total excision of the septum was performed. The patient underwent regular postoperative follow-ups for stenosis prevention.

Conclusion

Considering the rarity of these concurrent conditions, clinicians must always consider the possibility of several complex anomalies. Vaginoscopy using a hysteroscope may be useful for definitive diagnosis and determining appropriate treatments.

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一名有处女膜穿孔病史的少女的阴道横隔:病例报告
导言:无孔处女膜和阴道横隔是以阻塞性缺陷为特征的疾病,通常会导致在青春期前后发现血精。我们遇到过这样一位患者,她在婴儿时期接受了处女膜切开术,以治疗因处女膜无孔而导致的脓性阴道炎,后来在青春期因阴道横隔而出现血精。她在 3 个月大时曾患过脓性结肠炎和尿路感染。当时,会阴部检查未发现阴道口,诊断为处女膜未穿孔。在进行处女膜切开术时,阴道内支气管镜检查没有发现宫颈外口。然而,这一异常发现并未得到充分调查。处女膜切开术后无并发症,患者直到月经初潮前一直没有症状。月经初潮后 3 个月,生殖器检查发现阴道内有一个凸起的横隔膜,距离处女膜 5 厘米。超声波和磁共振成像显示子宫膨胀,上阴道膨胀,下阴道塌陷。考虑为阴道横隔,患者接受了阴道镜检查,以排除阴道闭锁或之前手术造成的粘连。阴道横隔的诊断得到了证实,并对阴道横隔进行了全切。结论考虑到这些并发症的罕见性,临床医生必须始终考虑多种复杂异常的可能性。使用宫腔镜进行阴道镜检查可能有助于明确诊断和确定适当的治疗方法。
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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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