Anand S K, Northway J D, Smith J A
Am J Dis Child. 1977 Jul;131(7):773-7. doi: 10.1001/archpedi.1977.02120200055011.
Renal papillary and cortical necrosis (RPCN) in newborn infants has been generally fatal. This report describes three survivors of neonatal RPCN who have been followed up from 23 to 57 months. The cause of RPCN was hemorrhage and asphyxia neonatorum in two patients and hemorrhage and shock in one. The diagnosis was confirmed in one patient by an excretory urogram at 3 weeks of age and in another by renal biopsy at 5 weeks of age. In the third, diagnosis was made retrospectively. Findings from subsequent examination showed that creatinine clearance was normal in one patient, slightly reduced in another, and moderately reduced in the third. Maximum ability to concentrate urine was decreased in all. Follow-up excretory urograms in all three patients showed dilated bizarre-appearing calices and renal cortical atrophy. These radiologic findings are similar to those found in segmental hypoplasia or chronic (atrophic) pyelonephritis.
新生儿肾乳头和皮质坏死(RPCN)通常是致命的。本报告描述了3例新生儿RPCN幸存者,随访时间为23至57个月。2例患者RPCN的病因是新生儿出血和窒息,1例是出血和休克。1例患者在3周龄时通过排泄性尿路造影确诊,另1例在5周龄时通过肾活检确诊。第3例为回顾性诊断。后续检查结果显示,1例患者肌酐清除率正常,另1例略有降低,第3例中度降低。所有人的最大尿浓缩能力均下降。所有3例患者的随访排泄性尿路造影均显示肾盂盏扩张、形态怪异及肾皮质萎缩。这些放射学表现与节段性肾发育不全或慢性(萎缩性)肾盂肾炎的表现相似。