Literature DB >> 12836092

Hemolytic uremic syndrome associated with group A beta-hemolytic streptococcus.

Amy B Shepherd1, April L Palmer, Steven A Bigler, Radhakrishna Baliga.   

Abstract

Group A beta-hemolytic streptococcal (GABS) hemorrhagic colitis due to Streptococcus pyogenes is extremely rare and its association with hemolytic uremic syndrome (HUS) in children has not been described. We report a 9-year-old white male who developed biopsy-proven HUS while continuing to have GABS-positive bloody diarrhea. Renal function deteriorated rapidly requiring intermittent hemodialysis. Three months following discharge, his renal function is normal for age except for significant proteinuria.

Entities:  

Mesh：

Year:  2003        PMID： 12836092     DOI： 10.1007/s00467-003-1191-4

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


  10 in total

Review 1.  Thrombotic microangiopathies.

Authors:  Joel L Moake
Journal:  N Engl J Med       Date:  2002-08-22       Impact factor: 91.245

2.  Hemorrhagic colitis with Streptococcus pyogenes preceding hemolytic uremic syndrome during early pregnancy.

Authors:  P E Bollaert; P Bauer; P Judlin; M C Laprevote-Heully; H Lambert; A Larcan
Journal:  Nephron       Date:  1989       Impact factor: 2.847

3.  Activation of a 66-kilodalton human endothelial cell matrix metalloprotease by Streptococcus pyogenes extracellular cysteine protease.

Authors:  E H Burns; A M Marciel; J M Musser
Journal:  Infect Immun       Date:  1996-11       Impact factor: 3.441

4.  Group A beta-hemolytic streptococcal proctocolitis.

Authors:  C Guss; J G Larsen
Journal:  Pediatr Infect Dis       Date:  1984 Sep-Oct

5.  Acquisition of regulators of complement activation by Streptococcus pyogenes serotype M1.

Authors:  Vinod Pandiripally; Eugene Gregory; David Cue
Journal:  Infect Immun       Date:  2002-11       Impact factor: 3.441

Review 6.  Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura.

Authors:  P Ruggenenti; M Noris; G Remuzzi
Journal:  Kidney Int       Date:  2001-09       Impact factor: 10.612

7.  The complement system in hemolytic-uremic syndrome in childhood.

Authors:  L Monnens; J Molenaar; P H Lambert; W Proesmans; P van Munster
Journal:  Clin Nephrol       Date:  1980-04       Impact factor: 0.975

8.  Hypocomplementemia and leukocytosis in diarrhea-associated hemolytic uremic syndrome.

Authors:  W L Robson; A K Leung; G H Fick; A I McKenna
Journal:  Nephron       Date:  1992       Impact factor: 2.847

Review 9.  The hemolytic uremic syndrome.

Authors:  R L Siegler
Journal:  Pediatr Clin North Am       Date:  1995-12       Impact factor: 3.278

10.  Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura.

Authors:  M Noris; P Ruggenenti; A Perna; S Orisio; J Caprioli; C Skerka; B Vasile; P F Zipfel; G Remuzzi
Journal:  J Am Soc Nephrol       Date:  1999-02       Impact factor: 10.121
  10 in total
  1 in total

1.  Atypical hemolytic uremic syndrome associated with group A beta hemolytic streptococcus.

Authors:  Bilal Yildiz; Nurdan Kural; Coskun Yarar
Journal:  Pediatr Nephrol       Date:  2004-06-16       Impact factor: 3.714
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.