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肛肠畸形

Anorectal malformations.

作者信息

Peña A

机构信息

Department of Surgery, Schneider Children's Hospital, Long Island Jewish Medical Center, New Hyde Park, NY 11040, USA.

出版信息

Semin Pediatr Surg. 1995 Feb;4(1):35-47.

PMID:7728507
Abstract

The posterior sagittal approach was used to treat 792 patients with anorectal malformations. From these, 387 cases were evaluated 6 months to 13 years later. Voluntary bowel movements were present in 74.3% of the entire series. When distributed by diagnosis, the percentages varied: 100% in patients with rectal atresia and perineal fistula; 93.2% in those with vestibular fistula; 80.9% in those with bulbar fistula; 71.1% in those with cloacas; 66.7% in those with prostatic fistula, and 15.8% in those with bladder-neck fistula. Soiling was present in 57% of all cases. Patients with voluntary bowel movements and no soiling were classified as totally continent; 40.8% of the series belong to this group. Distributed by diagnosis, it varied from 100% in cases with rectal atresia or perineal fistula, 65.9% in those with vestibular fistula, 34% in those with bulbar fistula, 31.6% in those with cloacas, 26.3% in those with prostatic fistula; none of the patients with vaginal fistula or bladder-neck fistula was totally continent. Constipation was detected in 43.1% of all patients, and was more frequent in those with simple defects. Urinary incontinence was found in 19% of patients with cloacas who had a common channel shorter than 3 cm, and in 68.8% of the patients who had longer common channels. Other patients suffered from urinary incontinence only when they had an absent sacrum or other severe bladder or urethral congenital defects. An accurate diagnosis and evaluation of the sacrum allows us to establish, with reasonable accuracy, functional prognosis in most children. Those with functional disorders must be treated properly medically, to improve their quality of life.

摘要

采用后矢状入路治疗792例肛门直肠畸形患者。其中,387例在6个月至13年后接受评估。整个系列中74.3%的患者能够自主排便。按诊断分类,百分比有所不同:直肠闭锁合并会阴瘘患者为100%;前庭瘘患者为93.2%;球部瘘患者为80.9%;泄殖腔畸形患者为71.1%;前列腺瘘患者为66.7%;膀胱颈瘘患者为15.8%。57%的所有病例存在污粪情况。能够自主排便且无污粪的患者被归类为完全可控便;该系列中40.8%的患者属于这一组。按诊断分类,直肠闭锁或会阴瘘病例为100%,前庭瘘患者为65.9%,球部瘘患者为34%,泄殖腔畸形患者为31.6%,前列腺瘘患者为26.3%;阴道瘘或膀胱颈瘘患者无一例完全可控便。43.1%的所有患者存在便秘,且在单纯缺陷患者中更为常见。泄殖腔畸形患者中,共同管短于3 cm的患者有19%存在尿失禁,共同管较长的患者有68.8%存在尿失禁。其他患者仅在骶骨缺如或存在其他严重膀胱或尿道先天性缺陷时出现尿失禁。对骶骨进行准确诊断和评估使我们能够在大多数儿童中合理准确地确定功能预后。有功能障碍的患者必须接受适当的医学治疗,以提高他们的生活质量。

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