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1.
Indian J Pediatr ; 2006 May; 73(5): 401-4
Article Dans Anglais | IMSEAR | ID: sea-80584

Résumé

OBJECTIVES: Brain abscess is a serious life-threatening complication of several diseases. The objective of this study was to look at the clinical profile of patients, predisposing conditions, microbiology and outcome of children suffering from brain abscess. METHODS: Thirty children aged less than 15 years were reviewed. There were 15 males and 15 females. The mean age of presentation was 5.6+/-4.4 years. RESULTS: The duration of illness at the time of admission was 17.6+/-24.6 days. Typically patients presented with fever, vomiting, headache and seizures. The predisposing conditions found were cyanotic congenital heart disease in 11 (37%) of children, meningitis in 6 (20%), septicemia in 7 (23%) and no underlying cause was found in 5 (17%) children. The most common microbe in children with cyanotic congenital heart disease was of the Streptococcus milleri group (52%). Computerized tomography confirmed the diagnosis and the most common location of the abscess was the parietal lobe of the cerebral hemisphere. All abscesses were large, more than 2 cm in diameter and were aspirated surgically. Excision was performed in 6 children. Five children expired, one due to a intracranial bleeding and the others due to severe cerebral edema and tentorial herniation. Complications were seen in 20 children and 16 had sequelae, hemiparesis in 11 and seizure disorder in 5. CONCLUSION: Brain abscess is a serious infection with poor outcome if diagnosed late. Delayed surgical drainage has high morbidity and mortality. The threshold for diagnosis should be low, particularly in children with a predisposing condition like cyanotic congenital heart disease.


Sujets)
Adolescent , Abcès cérébral/étiologie , Causalité , Enfant , Enfant d'âge préscolaire , Cyanose , Drainage , Femelle , Cardiopathies congénitales/complications , Humains , Nourrisson , Mâle , Lobe pariétal , Études rétrospectives , Infections à streptocoques/complications , Groupe des streptocoques milleri , Résultat thérapeutique
2.
JAMC-Journal of Ayub Medical College-Abbotabad-Pakistan. 2006; 18 (2): 21-24
Dans Anglais | IMEMR | ID: emr-77316

Résumé

Cerebral abscess is a serious life threatening complication of several diseases. The objective of this study was to look at the clinical profile, microbiology and outcome of children with cerebral abscess having an underlying congenital heart disease as compared to other predisposing conditions. Thirty children aged less than 15 years were reviewed. There were 15 males and 15 females. The mean age of presentation was 5.6 +/- 4.4 years. The duration of illness at the time of admission was 17.6 +/- 24.6 days. Typically patients presented with fever, vomiting, headache and seizures. The predisposing conditions found were cyanotic congenital heart disease in 11 [37%] of children, meningitis in 6 [20%], septicemia in 7 [23%] and no underlying cause was found in 5 [17%] children. The most common microbe in children with cyanotic congenital heart disease was of the Streptococcus milleri group [52%]. Computerized tomography confirmed the diagnosis and the most common location of the abscess was the parietal lobe of the cerebral hemisphere. All abscesses were large, more than 2 cm in diameter and were aspirated surgically. Excision was performed in 6 children. Five children expired, one due to an intracranial bleeding and the others due to severe cerebral edema and tentorial herniation. Complications were seen in 20 children and 16 had sequelae, hemiparesis in 11 and seizure disorder in 5. Brain abscess is a serious infection with poor outcome if diagnosed late. Delayed surgical drainage has high morbidity and mortality. The threshold for diagnosis should be low particularly in children with a predisposing condition like cyanotic congenital heart disease


Sujets)
Humains , Mâle , Femelle , Abcès cérébral/microbiologie , Cardiopathies congénitales , Cyanose , Études rétrospectives ,
3.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2005; 15 (5): 302-303
Dans Anglais | IMEMR | ID: emr-71559

Résumé

Isolated non-compaction of the left ventricle is a distinct form of cardiomyopathy. It may be idiopathic or secondary to an identifiable disease. The condition usually presents with symptoms of cardiac failure. The present report is of a child with this disease who was diagnosed at birth and was relatively stable at 5 years of age


Sujets)
Humains , Mâle , Ventricules cardiaques/malformations , Défaillance cardiaque/étiologie , Études de suivi , Cardiomyopathies/anatomopathologie , Myocarde/anatomopathologie
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