Scientific Electronic Library Online

 
vol.36 no.2Diagnósticos Dermatopatológicos Tumorales en la Población Pediátrica. Cátedra de Dermatología del Hospital de Clínicas  índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Pediatría (Asunción)
ISSN 1683-9803 versão on-line

 
 
Como citar este artigo
 
 

Resumo

CHAMORRO NOCEDA, Luis Alberto. Síndrome Urémico-Hemolítico por E. Coli Entero-Hemorrágica 0157:H7 Stx2: Primer Caso Descrito en Paraguay. Pediatr. (Asunción), Ago. 2009, vol.36, no.2, p.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.

Palavras-chave: Hemolytic anemia; thrombocytopenia; Escherichia coli; 0157:H7; Shiga toxin type 2; Paraguay.

        · resumo em espanhol     · texto em espanhol     · pdf em espanhol


 

© 2014  Sociedad Paraguaya de Pediatría

Mcal. Estigarribia 1764 c/ Rca. Francesa
Asunción - Paraguay
Tel.: 0595 021 447 493



revista@spp.org.py