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Sigmoid colon vaginoplasty in children.

机译:乙状结肠儿童阴道成形术。

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BACKGROUND: Vaginal construction is necessary for the patients with aplasia of Mullerian ducts, testicular feminisation and androgen insensitivity syndromes. Many methods of vaginal construction have been described. We report here the outcomes of six adolescent patients who underwent sigmoid colon vaginoplasty with special emphasis on the surgical technique and outcomes. PATIENTS AND METHODS: Between 1990 and 2003, six patients underwent sigmoid vaginoplasty after a diagnosis of 5alpha-reductase deficiency (n = 3), testicular feminisation (n = 2) or vaginal atresia (n = 1). The mean age was 16 years (13 to 18). Wide spectrum antibiotics and whole-gut preparation were used in all cases. A 15-20 cm segment of sigmoid colon was pulled through the retrovesical tunnel. The proximal end was closed in two layers in patients with 5alpha-reductase deficiency and with testicular feminisation. A distal anastomosis was carried out to the opening made on the vaginal plate (5alpha-reductase deficiency) or on the tipof the shallow rudimentary vagina (testicular feminisation). The sigmoid segment was interposed between the blind end of the atretic vagina and the perineum in the patient with vaginal atresia. Patients were instructed to perform daily vaginal irrigation. The neovagina was examined and calibrated under anaesthesia. No routine vaginal dilatation was recommended. RESULTS: All but one patient had an uneventful postoperative period and were discharged within 7-8 days. All patients had an excellent cosmetic result with an appropriate vaginal length. One of the patients experienced late stenosis of the introitus which responded to dilatations. Mucus discharge was not a significant problem. The patient with vaginal atresia (Bardet-Biedl syndrome) experienced deep vein thrombosis, renal failure and sepsis, resulting in death. CONCLUSION: Sigmoid colon vaginoplasty is a special procedure which appears appropriate for the construction of a new vagina in children. A sigmoid colon neovagina meets all necessary criteria after a vaginoplasty. It provides an adequate diameter and length, and produces less scar tissue in the perineum. It is self-moistening, easily adaptable to the uterus, cervix and rudimentary atretic vaginal segments and does not require routine dilatation. Mild stenosis of the introitus can be treated by dilatations and revision can be easily performed in severely stenotic cases. On the other hand, the patient may face morbidity after laparotomy and other serious complications may occur due to accompanying diseases.
机译:背景:对于穆勒管发育不全,睾丸女性化和雄激素不敏感综合征的患者,必须进行阴道建造。已经描述了许多阴道构造方法。我们在这里报告了六名接受乙状结肠阴道成形术的青春期患者的结局,特别强调了手术技术和结局。患者与方法:1990年至2003年间,有6例患者被诊断为5α-还原酶缺乏症(n = 3),睾丸女性化(n = 2)或阴道闭锁(n = 1)后进行了乙状结肠成形术。平均年龄为16岁(13至18岁)。在所有情况下均使用广谱抗生素和全肠制剂。将15-20cm的乙状结肠段拉过膀胱后隧道。 5alpha-还原酶缺乏症和睾丸女性化患者的近端分为两层。远端吻合术是在阴道板(5α-还原酶缺乏症)或浅浅的阴道尖端(睾丸女性化)上的开口处进行的。乙状结肠节段介于阴道闭锁患者的闭路阴道的盲端和会阴之间。指导患者每天进行阴道冲洗。在麻醉下检查并校准新阴道。不建议常规的阴道扩张术。结果:除1例患者外,其余患者术后均顺利,并于7-8天内出院。所有患者均具有良好的美容效果,阴道长度合适。一名患者经历了扩张的晚期口肌狭窄。粘液排出不是重大问题。阴道闭锁(Bardet-Biedl综合征)患者经历深静脉血栓形成,肾衰竭和败血症,导致死亡。结论:乙状结肠阴道成形术是一种特殊的方法,似乎适合于儿童新阴道的构建。阴道成形术后乙状结肠新阴道符合所有必要标准。它提供足够的直径和长度,并在会阴部产生较少的疤痕组织。它具有自我滋润作用,易于适应子宫,子宫颈和原始的闭锁性阴道段,无需常规扩张。轻度狭窄者可通过扩张术治疗,严重狭窄者可轻易进行翻修。另一方面,患者可能会在剖腹手术后面临发病,并且由于伴随疾病可能会发生其他严重的并发症。

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