Genest D R, Lage J M
Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115.
Hum Pathol. 1991 Feb;22(2):147-53. doi: 10.1016/0046-8177(91)90036-o.
Rare fetuses and neonates with kidneys lacking normal-appearing proximal tubules have been described. In order to ascertain the prevalence of this histologic finding, and to study its associated clinicopathologic features, 500 consecutive perinatal autopsies (performed from 1981 to 1985) were reviewed. Kidneys lacking normal-appearing proximal tubules were found in six of 500 (1.2%) perinatal autopsies (one liveborn and five stillborn cases). The liveborn infant was one of a sibship with renal tubular dysgenesis. Four of the stillborn fetuses were derived from monochorionic twin gestations; the histologic abnormality was present in only one fetus from each twin pair. Three of the four twin pairs had pathologic features suggestive of twin-to-twin transfusion, with the renal abnormality present in the donor twin; renal hypoplasia existed in two instances. The fourth affected twin was a stillborn acardiac fetus with multiple congenital anomalies and unilateral renal agenesis. The fifth stillborn was a hydropic fetus with trisomy 21 and renal hypoplasia. In this series, lack of recognizable renal proximal tubules most often was not a manifestation of renal tubular dysgenesis. The histologic finding was associated with stillborn, renal hypoplasia, and congenital anomalies, and was strongly associated with monochorionic twinning (P = 0.001). In the stillborn cases in this series, we suggest that this finding may represent renal tubular degeneration resulting from renal hypoperfusion.
已有文献报道过罕见的胎儿和新生儿肾脏缺乏外观正常的近端肾小管。为了确定这一组织学发现的发生率,并研究其相关的临床病理特征,我们回顾了500例连续的围产期尸检(于1981年至1985年间进行)。在500例围产期尸检中有6例(1.2%)发现肾脏缺乏外观正常的近端肾小管(1例活产儿和5例死产儿)。该活产儿是患有肾小管发育不全的同胞之一。4例死产胎儿来自单绒毛膜双胎妊娠;每对双胞胎中只有1个胎儿存在组织学异常。4对双胞胎中有3对具有提示双胎输血的病理特征,肾脏异常出现在供血儿双胞胎中;有2例存在肾发育不全。第4例受影响的双胞胎是一个患有多种先天性异常和单侧肾缺如的死产无心畸胎。第5例死产儿是一个患有21三体综合征和肾发育不全的水肿胎儿。在本系列研究中,无法识别的肾近端肾小管缺乏最常见的并非是肾小管发育不全的表现。这一组织学发现与死产、肾发育不全和先天性异常相关,并且与单绒毛膜双胎密切相关(P = 0.001)。在本系列的死产病例中,我们认为这一发现可能代表了肾灌注不足导致的肾小管变性。