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The Exstrophy-epispadias complex

机译:Exstrophy-上棘膜复合体

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摘要

Exstrophy-epispadias complex (EEC) represents a spectrum of genitourinary malformations ranging in severity from epispadias (E) to classical bladder exstrophy (CEB) and exstrophy of the cloaca (EC). Depending on severity, EEC may involve the urinary system, musculoskeletal system, pelvis, pelvic floor, abdominal wall, genitalia, and sometimes the spine and anus. Prevalence at birth for the whole spectrum is reported at 1/10,000, ranging from 1/30,000 for CEB to 1/200,000 for EC, with an overall greater proportion of affected males. EEC is characterized by a visible defect of the lower abdominal wall, either with an evaginated bladder plate (CEB), or with an open urethral plate in males or a cleft in females (E). In CE, two exstrophied hemibladders, as well as omphalocele, an imperforate anus and spinal defects, can be seen after birth. EEC results from mechanical disruption or enlargement of the cloacal membrane; the timing of the rupture determines the severity of the malformation. The underlying cause remains unknown: both genetic and environmental factors are likely to play a role in the etiology of EEC. Diagnosis at birth is made on the basis of the clinical presentation but EEC may be detected prenatally by ultrasound from repeated non-visualization of a normally filled fetal bladder. Counseling should be provided to parents but, due to a favorable outcome, termination of the pregnancy is no longer recommended. Management is primarily surgical, with the main aims of obtaining secure abdominal wall closure, achieving urinary continence with preservation of renal function, and, finally, adequate cosmetic and functional genital reconstruction. Several methods for bladder reconstruction with creation of an outlet resistance during the newborn period are favored worldwide. Removal of the bladder template with complete urinary diversion to a rectal reservoir can be an alternative. After reconstructive surgery of the bladder, continence rates of about 80% are expected during childhood. Additional surgery might be needed to optimize bladder storage and emptying function. In cases of final reconstruction failure, urinary diversion should be undertaken. In puberty, genital and reproductive function are important issues. Psychosocial and psychosexual outcome depend on long-term multidisciplinary care to facilitate an adequate quality of life.
机译:上溢-上肢膜外复合体(EEC)代表一系列泌尿生殖道畸形,其严重程度从上溢(E)到经典膀胱外溢(CEB)和泄殖腔(EC)外溢。根据严重程度,EEC可能涉及泌尿系统,肌肉骨骼系统,骨盆,骨盆底,腹壁,生殖器,有时还包括脊柱和肛门。据报道,整个出生时的患病率为1 / 10,000,范围从CEB的1 / 30,000到EC的1 / 200,000,受影响男性的总体比例更高。 EEC的特征是下腹壁可见缺损,雄性为开腹膀胱板(CEB),尿道开放性为开孔,雌性则为裂口(E)。在CE中,出生后可以看到两个外生的半囊以及肛门无孔和脊柱缺损的卵圆形膨出。 EEC是由于泄殖腔膜的机械破裂或增大而导致的;破裂的时机决定了畸形的严重程度。根本原因仍然未知:遗传因素和环境因素均可能在EEC的病因中起作用。出生时的诊断是根据临床表现进行的,但是可以通过反复检查正常填充的胎儿膀胱,通过超声在产前检测到EEC。应该向父母提供咨询,但由于结果良好,不再建议终止妊娠。治疗主要是外科手术,其主要目的是获得安全的腹壁闭合,在保持肾功能的情况下实现尿失禁,最后进行适当的美容和功能性生殖器重建。在全球范围内,有几种在新生儿期产生出口阻力的膀胱重建方法。在完全将尿液转移至直肠储存器的情况下,取走膀胱模板是另一种选择。膀胱重建手术后,儿童期的节制率有望达到80%。可能需要进行其他手术以优化膀胱的存储和排空功能。如果最终重建失败,应进行尿流改道。在青春期,生殖器和生殖功能是重要的问题。社会心理和性倾向的结果取决于长期的多学科护理,以促进适当的生活质量。

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