Suppr超能文献

膀胱外翻-尿道上裂复合畸形的解剖学矫正:34例患者分析

Anatomical correction of the exstrophy-epispadias complex: analysis of 34 patients.

作者信息

Nicholls G, Duffy P G

机构信息

Department of Paediatric Urology, Great Ormond Street Hospital for Children NHS Trust, London, UK.

出版信息

Br J Urol. 1998 Dec;82(6):865-9. doi: 10.1046/j.1464-410x.1998.00885.x.

Abstract

OBJECTIVE

To evaluate the surgical procedures required for anatomical reconstruction of the bladder and penis in the exstrophy-epispadias complex.

PATIENTS AND METHODS

All primary exstrophy-epispadias repairs carried out by one surgeon between 1987 and 1997 were reviewed. Bladder closure consisted of full extraperitoneal mobilization, transpositional omphaloplasty, drainage with ureteric and urethral catheters and immobilization with a 'frog-leg' plaster-cast or 'mermaid' dressings. Osteotomies were always performed when bladder closure was attempted after 37 h of age. Before 1990 the osteotomies were posterior vertical iliac (one patient) and subsequently anterior oblique iliac (10 patients). Pre-peritoneal herniotomies, in the absence of a clinical hernia, were included in the primary procedure after 1992. A modified Cantwell technique was used for epispadias repair and this was undertaken at a median of 16 months after bladder closure (range 6-30).

RESULTS

Thirty-four patients (27 male) were reviewed; one patient had a chromosomal abnormality, a deletion in the short arm of chromosome 4. The male infants required a median of four procedures (range 2-5) for bladder closure, epispadias reconstruction and herniotomies, while the females needed a median of two (range 2-5). Complete bladder dehiscence, requiring re-closure with osteotomies, occurred in three cases (9%, two male). There were no dehiscences in the primary osteotomy group. Fistulae after epispadias repair occurred in four patients (17%). The bladder capacity increased to > 60 mL in 10 of 15 males by 36 months after epispadias repair. Only two of seven female infants attained a capacity of > 60 mL. Of the 15 infants who did not undergo herniotomy at primary closure, 13 subsequently developed inguinal hernias (one uni- and 11 bilateral) with incarceration occurring in two. Twelve infants underwent herniotomy at primary closure and six developed subsequent hernias (two uni- and four bilateral; P = 0.05) with documented incarceration in two.

CONCLUSIONS

Anatomical correction of the exstrophy-epispadias complex remains challenging, but can be achieved with complication rates of < 20% for each stage. Bladder volumes large enough to permit adequate bladder neck reconstruction can be anticipated after epispadias repair in a large proportion of male infants, but remains small in female infants with low outlet resistance. Inguinal herniotomy at the time of bladder closure significantly reduces the incidence of subsequent herniation, which nevertheless remains high.

摘要

目的

评估膀胱外翻-尿道上裂复合畸形中膀胱和阴茎解剖重建所需的手术方法。

患者与方法

回顾了1987年至1997年间由一名外科医生进行的所有原发性膀胱外翻-尿道上裂修复手术。膀胱关闭包括完全腹膜外游离、移位脐成形术、输尿管和尿道导管引流以及用“蛙腿”石膏固定或“美人鱼”敷料固定。当在37小时龄后尝试关闭膀胱时总是进行截骨术。1990年前截骨术为后垂直髂骨截骨(1例患者),随后为前斜髂骨截骨(10例患者)。在1992年后,在无临床疝的情况下,腹膜前疝修补术被纳入初次手术。采用改良的坎特韦尔技术修复尿道上裂,该手术在膀胱关闭后中位时间16个月(范围6 - 30个月)进行。

结果

共回顾了34例患者(27例男性);1例患者有染色体异常,为4号染色体短臂缺失。男性婴儿进行膀胱关闭、尿道上裂重建和疝修补术平均需要4次手术(范围2 - 5次),而女性平均需要2次(范围2 - 5次)。3例患者(9%,2例男性)发生完全性膀胱裂开,需要再次关闭并进行截骨术。初次截骨组无裂开情况。尿道上裂修复后4例患者(17%)出现瘘管。尿道上裂修复后36个月,15例男性中有10例膀胱容量增加至>60 mL。7例女婴中只有2例容量>60 mL。15例在初次关闭时未进行疝修补术的婴儿中,13例随后发生腹股沟疝(1例单侧和11例双侧),其中2例发生嵌顿。12例婴儿在初次关闭时进行了疝修补术,6例随后发生疝(2例单侧和4例双侧;P = 0.05),其中2例有嵌顿记录。

结论

膀胱外翻-尿道上裂复合畸形的解剖矫正仍然具有挑战性,但每个阶段的并发症发生率可<20%。在大部分男性婴儿尿道上裂修复后,可以预期膀胱容量足够大以允许进行充分的膀胱颈重建,但女性婴儿出口阻力低时膀胱容量仍然较小。膀胱关闭时进行腹股沟疝修补术可显著降低随后疝形成的发生率,但其发生率仍然较高。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验