Literature DB >> 11465804

Acquired glomerulocystic kidney disease following hemolytic uremic syndrome.

F Emma1, A O Muda, S Rinaldi, R Boldrini, C Bosman, G Rizzoni.   

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.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11465804     DOI: 10.1007/s004670100608

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  2 in total

1.  A case report of thin basement membrane nephropathy accompanied by sporadic glomerulocystic kidney disease.

Authors:  Hiroyuki Hashimoto; Naro Ohashi; Naoko Tsuji; Yoshitaka Naito; Shinsuke Isobe; Tomoyuki Fujikura; Takayuki Tsuji; Akihiko Kato; Kandai Nozu; Kazumoto Iijima; Hideo Yasuda
Journal:  BMC Nephrol       Date:  2019-07-09       Impact factor: 2.388

Review 2.  Glomerulocystic kidney disease.

Authors:  John J Bissler; Brian J Siroky; Hong Yin
Journal:  Pediatr Nephrol       Date:  2010-01-21       Impact factor: 3.714

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.