Two-balloon epistaxis catheter to ensure vaginal patency in a complex case of vaginoplasty for vaginal agenesis: a case report.

Q3 Medicine Pediatria Medica e Chirurgica Pub Date : 2023-11-27 DOI:10.4081/pmc.2023.318
Chiara Costantini, Federica Fati, Elisa Pani, Fabio Beretta, Silvia Bisoffi, Giosuè Mazzero, Elisa Negri, Clara Revetria, Hamid R Sadri, Enrico Ciardini
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Abstract

Congenital vaginal atresia is a rare anomaly of the female genital tract. Many vaginoplasty procedures have been described, but the postoperative risk of vaginal stenosis remains a challenge. We report a case of isolated distal vaginal agenesis in a patient with neurological impairment where the use of an "alternative" dilator was needed. An 11-year-old girl with Down syndrome was admitted to the Emergency Department complaining of pelvic pain. The clinical evaluation showed a hard and painful pelvic mass associated with an imperforate hymen. Abdominal ultrasound and pelvic MRI were suggestive for hematometrocolpos and absence of the lower third segment of the vagina. Vaginoscopy confirmed the diagnosis of congenital vaginal agenesis. The patient then underwent a laparoscopic-assisted vaginoplasty. Considering the difficult management of the postoperative period, an epistaxis catheter was used as a vaginal stent and dilator. The use of an epistaxis catheter to provide adequate vaginal patency after vaginoplasty can be an alternative solution especially in those cases where calibrations with dilators are difficult or not tolerated.

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双气囊鼻出血导管在阴道发育不全的复杂阴道成形术中确保阴道通畅:一例报告。
摘要先天性阴道闭锁是一种罕见的女性生殖道异常。许多阴道成形术已经被描述,但阴道狭窄的术后风险仍然是一个挑战。我们报告一例孤立性阴道远端发育不全的患者与神经损伤,其中使用“替代”扩张器是必要的。一名患有唐氏综合症的11岁女孩因骨盆疼痛被送往急诊科。临床评估显示硬而疼痛的盆腔肿块伴处女膜闭锁。腹部超声和盆腔MRI提示有阴道出血和阴道下三段缺失。阴道镜检查证实诊断为先天性阴道发育不全。患者随后接受了腹腔镜辅助阴道成形术。考虑到术后处理困难,我们使用鼻出血导管作为阴道支架和扩张器。阴道成形术后使用鼻出血导管提供足够的阴道通畅是一种替代解决方案,特别是在使用扩张器校准困难或不耐受的情况下。
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来源期刊
Pediatria Medica e Chirurgica
Pediatria Medica e Chirurgica Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.70
自引率
0.00%
发文量
21
审稿时长
10 weeks
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