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1.
An Esp Pediatr ; 39(2): 111-5, 1993 Aug.
Article in Spanish | MEDLINE | ID: mdl-8239205

ABSTRACT

We report the epidemiology of invasive Haemophilus influenzae type B infections. The study is based on 58 children and was carried out during the years from 1981 to 1990. Sixty-three percent of the patients had meningitis, 10.3% had arthritis, 10.3% had epiglottitis, 8.6% had cellulitis and 6.9% had pneumonia. Thirteen percent of the cases were children who were less than 6 months old, 34.4% were less than 12 months old, 70.6% were less than 24 months of age and 93% were less than 4 years old. Among the latter, 90% of the children with epiglottis or pneumonia were 24 months or older compared with 16% of the patients with meningitis, arthritis or cellulitis (p < 0.001). Sixty-three percent of the isolated strains of Haemophilus influenzae type B were resistant to ampicillin and 19.2% of the strains were resistant to ampicillin and chloramphenicol.


Subject(s)
Haemophilus Infections/epidemiology , Haemophilus influenzae/isolation & purification , Age Factors , Ampicillin/pharmacology , Arthritis/epidemiology , Arthritis/microbiology , Cellulitis/epidemiology , Cellulitis/microbiology , Child, Preschool , Chloramphenicol/pharmacology , Drug Resistance, Microbial , Epiglottitis/diagnosis , Epiglottitis/epidemiology , Epiglottitis/microbiology , Female , Haemophilus Infections/diagnosis , Haemophilus Infections/microbiology , Haemophilus influenzae/drug effects , Humans , Infant , Male , Meningitis, Haemophilus/diagnosis , Meningitis, Haemophilus/epidemiology , Pneumonia/diagnosis , Pneumonia/epidemiology , Pneumonia/microbiology , Serotyping , Spain/epidemiology
2.
An Esp Pediatr ; 36(3): 181-5, 1992 Mar.
Article in Spanish | MEDLINE | ID: mdl-1580425

ABSTRACT

In this paper we report a review of the omphalic pathology that was admitted to our hospital from january 1973 through december 1990. Eleven cases of Beckwith-Wiedemann Syndrome were diagnosed during this period of time. Our eleven cases comply with at least three of the four major criteria (omphalocele, macroglossia, gigantism and neonatal hypoglycemia) and several of the minor criteria. The interest of this paper is based on the rareness of this syndrome and its association in two of our cases with Cacchi-Ricci Syndrome. Moreover, one of these cases later presented with a Wilms' tumor. Finally, we emphasize the importance of an early diagnosis of this syndrome in order to avoid the metabolic disturbances (hypoglycemia), to establish prompt treatment of the serious anomalies (omphalocele) and to control and follow these patients since they have increased risk to develop neoplastic disease.


Subject(s)
Beckwith-Wiedemann Syndrome/epidemiology , Female , Humans , Infant, Newborn , Male , Spain/epidemiology
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