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Acquired glomerulocystic kidney disease following hemolytic uremic syndrome.

作者信息

Emma F, Muda A O, Rinaldi S, Boldrini R, Bosman C, Rizzoni G

机构信息

Division of Nephrology, Children's Hospital and Research Institute Bambino Gesu', Rome, Italy.

出版信息

Pediatr Nephrol. 2001 Jul;16(7):557-60. doi: 10.1007/s004670100608.

DOI:10.1007/s004670100608
PMID:11465804
Abstract

Glomerulocystic kidney disease (GCKD) is a rare congenital condition that is usually reported in infants and young children. Only five cases of acquired GCKD after an acquired renal disease have been reported. Among these, two patients have developed cystic glomerular lesions following hemolytic uremic syndrome (HUS). We report a third case in a 2-year-old patient with this association. Common features between these three cases include atypical HUS, development of GCKD after prolonged peritoneal dialysis treatment, severe hypertension, and normal-sized kidneys without development of macroscopic cysts. Pathology findings in our patient include heavy expression of epidermal growth factor receptor in proximal tubules and evidence of obstruction of the glomerular outflow. We speculate that cystic dilatation of the Bowman's capsule may be secondary to ischemic lesions leading to proximal tubular obstruction.

摘要

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A case report of thin basement membrane nephropathy accompanied by sporadic glomerulocystic kidney disease.一份伴有散发性肾小球囊性病的薄基底膜肾病病例报告。
BMC Nephrol. 2019 Jul 9;20(1):248. doi: 10.1186/s12882-019-1451-6.
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Glomerulocystic kidney disease.肾小球囊状肾病。
Pediatr Nephrol. 2010 Oct;25(10):2049-56; quiz 2056-9. doi: 10.1007/s00467-009-1416-2. Epub 2010 Jan 21.