SciELO - Scientific Electronic Library Online

 
vol.36 issue2Dermatopathological Diagnosis of Tumors in a Pediatric Population Dermatology Department of the Hospital de Clinicas author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Pediatría (Asunción)

On-line version ISSN 1683-9803

Abstract

CHAMORRO NOCEDA, Luis Alberto. Hemolytic Uremic Syndrome Caused by Shiga Toxin type 2 Produced by Enterohemorrhagic Escherichia coli O157:H7: First Case Described in Paraguay. Pediatr. (Asunción) [online]. 2009, vol.36, n.2, pp.127-132. ISSN 1683-9803.

Hemolytic uremic syndrome is a clinical syndrome characterized by a diagnostic triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure. We present the case of an infant over two years of age who presented with an episode of bloody flux. On day 5 the patient was hospitalized with the symptom triad of hemolytic anemia, acute renal failure, and thrombocytopenia, which are characteristic of hemolytic uremic syndrome with diarrhea (D+ HUS) requiring transfusion of red blood cell concentrate due to severe hemolytic anemia, while the acute renal failure and thrombocytopenia were of mild intensity. The child’s condition improved and he was discharged after 48 hours in good condition. The fecal culture was positive for Escherichia coli O157:H7 Stx2, a known causative agent of the syndrome, making this the first such case reported in Paraguay.

Keywords : Hemolytic anemia; thrombocytopenia; Escherichia coli; 0157:H7; Shiga toxin type 2; Paraguay.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License