Nakayama D K, Harrison M R, de Lorimier A A
J Pediatr Surg. 1986 Jan;21(1):43-5. doi: 10.1016/s0022-3468(86)80651-0.
Urethral obstruction due to posterior urethral valves (PUV) is a more lethal condition in the newborn than is commonly recognized. To study its prognosis when the diagnosis of PUV is made shortly after birth, cases of PUV presenting in the first week of life were reviewed. Eleven cases were seen at the University of California, San Francisco from 1974 to 1982. Five babies died, three within two hours of birth of respiratory insufficiency secondary to severe pulmonary hypoplasia, and two within three weeks with rapidly progressive renal failure. Of the six survivors, four exhibited respiratory difficulty (prolonged ventilatory support required in two, and bilateral pneumothoraces in two), three developed renal failure despite early urinary diversion, and one had renal tubular dysfunction. Only two infants had normal renal function after undergoing a successful series of reconstructions. Prune-belly syndrome and limb deformities were present in two surviving and two fatal cases. Although most cases of congenital hydronephrosis can be successfully treated after birth, those presenting in the newborn period represent a subset with high morbidity and mortality. With advances in prenatal diagnosis of congenital hydronephrosis, salvage of severe cases detected early in gestation may require more aggressive management in the prenatal period.
后尿道瓣膜(PUV)导致的尿道梗阻在新生儿中是一种比通常认为的更具致命性的病症。为了研究出生后不久诊断出PUV时的预后情况,对出生第一周出现PUV的病例进行了回顾。1974年至1982年期间,在加利福尼亚大学旧金山分校共诊治了11例。5例婴儿死亡,3例在出生后两小时内死于严重肺发育不全继发的呼吸功能不全,2例在三周内死于快速进展的肾衰竭。6例幸存者中,4例出现呼吸困难(2例需要长时间通气支持,2例发生双侧气胸),3例尽管早期进行了尿液改道仍发生肾衰竭,1例有肾小管功能障碍。只有2例婴儿在成功进行一系列重建手术后肾功能正常。2例存活和2例死亡病例中存在梅干腹综合征和肢体畸形。虽然大多数先天性肾积水病例在出生后可以成功治疗,但那些在新生儿期出现的病例是发病率和死亡率较高的一个亚组。随着先天性肾积水产前诊断的进展,对妊娠早期检测出的严重病例进行挽救可能需要在产前阶段采取更积极的管理措施。