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1.
J Postgrad Med ; 1997 Oct-Dec; 43(4): 106-8
Artículo en Inglés | IMSEAR | ID: sea-115572

RESUMEN

Chordoma, a rare malignant tumour of early adulthood, rarely presents in children. We report such a case of rare malignant tumour which was diagnosed in the first decade of life.


Asunto(s)
Preescolar , Cordoma/patología , Colostomía , Femenino , Humanos , Región Sacrococcígea , Neoplasias de la Columna Vertebral/patología , Tomografía Computarizada por Rayos X
2.
J Postgrad Med ; 1996 Oct-Dec; 42(4): 123-5
Artículo en Inglés | IMSEAR | ID: sea-116582

RESUMEN

We report three sibs with mild autosomal recessive variety of osteopetrosis. The prominent clinical features were short stature, malocclusion of teeth, hepatosplenomegaly and a typical facial appearance. The only atypical features were microcephaly, a normal upper segment to lower segment ratio and a normal arm span.


Asunto(s)
Niño , Preescolar , Femenino , Genes Recesivos/genética , Enfermedades Genéticas Congénitas/genética , Humanos , Lactante , Osteopetrosis/genética , Linaje
4.
J Postgrad Med ; 1996 Jul-Sep; 42(3): 84-6
Artículo en Inglés | IMSEAR | ID: sea-115234

RESUMEN

An eleven year old boy presented with sudden onset right-sided hemiplegia and ipsilateral lower facial weakness. Two-dimensional echo revealed the diagnosis of idiopathic dilated cardiomyopathy with multiple intracardiac clots. MRI scan of head showed infarctions in the area of caudate nuclei, putamen, brain stem and cerebellum. On anticoagulation therapy, all thrombi, except one, disappeared. The child died 2.5 months later due to resistant cardiac failure.


Asunto(s)
Anticoagulantes/uso terapéutico , Cardiomiopatía Dilatada/complicaciones , Infarto Cerebral/diagnóstico , Niño , Resultado Fatal , Humanos , Embolia y Trombosis Intracraneal/diagnóstico , Imagen por Resonancia Magnética , Masculino
7.
J Postgrad Med ; 1995 Oct-Dec; 41(4): 108-9
Artículo en Inglés | IMSEAR | ID: sea-115207

RESUMEN

The clinical profile of typhoid fever in an infant is variable and non-specific. A rare case of typhoid fever in a 7 month old infant is reported. The child presented with only a day's history of fever and loose motions which resulted in severe dehydration, acute tubular necrosis and death. The diagnosis of typhoid fever was made only on post-mortem study. The problem in diagnosing typhoid fever in a young infant is highlighted with a brief literature review on the subject.


Asunto(s)
Resultado Fatal , Femenino , Humanos , Lactante , Fiebre Tifoidea/diagnóstico
10.
J Postgrad Med ; 1994 Oct-Dec; 40(4): 204-7
Artículo en Inglés | IMSEAR | ID: sea-116861

RESUMEN

In 28 children, with bacteriologically and/or serologically diagnosed typhoid fever treated at KEM Hospital, Bombay in 1991, initially one of the three recommended drugs (viz. chloramphenicol, amoxycillin or co-trimoxazole) was given for 7 days for defervescence to occur. In those who failed to respond, a second trial of therapy with one of the other two drugs was initiated, after omitting the first drug. A second failure of therapy was taken as an indication to use ciprofloxacin singly. Eventually, 18 (64.3%) cases responded to chloramphenicol or amoxycillin or co-trimoxazole. Ciprofloxacin was used in 19(35.7%) cases. the failure rate of treatment with chloramphenicol was 50%, with amoxycillin 71.4%, with co-trimoxazole 75% and 0% with ciprofloxacin. An analysis of the 28 cases revealed that apart from fever (in 100%), splenomegaly (in 82.1%) was the most important clinical pointer to diagnosis, along with absolute eosinopenia (in 71.4%). There were no major complications, except 2 cases with typhoid hepatitis who responded to choramphenicol and co-trimoxazole, respectively. Blood culture grew Salmonella typhi in 7 cases, of which 5 (72%) were multidrug resistant S. typhi. There were no characteristic clinical features to identify multi-drug resistant typhoid fever.


Asunto(s)
Amoxicilina/uso terapéutico , Antiinfecciosos/uso terapéutico , Niño , Ciprofloxacina/uso terapéutico , Humanos , Penicilinas/uso terapéutico , Esplenomegalia , Combinación Trimetoprim y Sulfametoxazol/uso terapéutico , Fiebre Tifoidea/diagnóstico
11.
J Postgrad Med ; 1994 Jan-Mar; 40(1): 40-1
Artículo en Inglés | IMSEAR | ID: sea-115602

RESUMEN

A 2 1/2 month old male child was admitted with loose motions and mild dehydration. He was full term normal delivery, born of a non-consanguinous marriage. On examination, he had trigonocephaly; anteverted nostrils, long philtrum and hypoplastic supraorbital ridges. X-ray showed sutural separation. Karyotyping confirmed deletion of short arm of chromosome 9 distal to band p22.


Asunto(s)
Preescolar , Deleción Cromosómica , Cromosomas Humanos Par 9 , Disostosis Craneofacial/etiología , Humanos , Masculino , Cráneo/anomalías , Síndrome
13.
Artículo en Inglés | IMSEAR | ID: sea-93307

RESUMEN

Fifty-four consecutively referred patients with uncontrolled epilepsy were subjected to Therapeutic Drug Monitoring on an out patient basis. Regular 2 weekly follow up for a minimum period of 2 months was done, after altering the drug dosage and bringing plasma level(s) within therapeutic range. Plasma levels of Phenobarbitone, Phenytoin and Carbamezepine were done by High Pressure Liquid Chromatography. Eventually, 24 patients were controlled and 30 remained uncontrolled. Significant differences between these 2 groups were found, as regards, duration of epilepsy (p < 0.01), associated mental retardation (p < 0.02), initial carbamazepine dosage and plasma levels in patients on carbamazepine montherapy (p < 0.02 and P < 0.01, respectively) and final phenytoin plasma levels in patients on combined therapy with phenobarbitone and phenytoin (p < 0.05). This study emphasizes the importance of early diagnosis and treatment of epilepsy with the help of plasma level monitoring of anti-epileptic drugs.


Asunto(s)
Anticonvulsivantes/administración & dosificación , Carbamazepina/administración & dosificación , Esquema de Medicación , Monitoreo de Drogas , Quimioterapia Combinada , Epilepsia/tratamiento farmacológico , Femenino , Humanos , Masculino , Fenobarbital/administración & dosificación , Fenitoína/administración & dosificación , Insuficiencia del Tratamiento
15.
Indian Pediatr ; 1992 Feb; 29(2): 181-8
Artículo en Inglés | IMSEAR | ID: sea-13424

RESUMEN

Ciprofloxacin, a fluoroquinolone antibacterial agent, is not recommended in pediatric population on account of its possible adverse effect on growing cartilage. It is being commonly used for treatment of variety of infections in children in our country and very little information is available on the risks involved in its use. A questionnaire was sent to 750 pediatricians in the last week of November 1990, to retrospectively judge over the previous 2 month period the extent of its use and identify the adverse drug reactions (ADRs). One hundred and fifty-four pediatricians replied, of which 147 had prescribed ciprofloxacin in a total of 3341 patients under 18 years of age, enteric fever being the commonest indication for its use. One hundred and fifty-nine ADRs were reported in 104 (3.1%) patients. They were: gastrointestinal in 50% of these 104 patients, CNS in 23%, skin and allergic in 19.1%, musculoskeletal in 8.6%, hematological in 3.8%, CVS in 2.9% and nephrological in 0.9% cases. Of 159 ADRs, 8 (5%) were severe, 76 (47.8%) were moderate and 75 (47.2%) were mild. Therapy needed discontinuation in only 9 (0.3%) patients. Two new ADRs were identified, viz., sudden death after intravenous ciprofloxacin and sinus nodal arrest causing bradycardia.


Asunto(s)
Adolescente , Niño , Preescolar , Ciprofloxacina/efectos adversos , Humanos , Lactante , Encuestas y Cuestionarios , Estudios Retrospectivos
16.
Artículo en Inglés | IMSEAR | ID: sea-64269

RESUMEN

A prospective survey of laboratory records was carried out to identify the extent of drug induced hepatotoxicity in a hospital population. Eleven of 1000 (1.1%) abnormal liver function tests were due to drug induced hepatotoxicity. Anti-tubercular drugs, viz isoniazid, rifampicin and pyrazinamide were responsible for all cases of serious hepatotoxicity.


Asunto(s)
Adulto , Antituberculosos/efectos adversos , Femenino , Enfermedad Hepática Inducida por Sustancias y Drogas/epidemiología , Humanos , India/epidemiología , Lactante , Pruebas de Función Hepática , Masculino , Persona de Mediana Edad , Estudios Prospectivos
20.
J Postgrad Med ; 1991 Jan; 37(1): 58B, 59-61
Artículo en Inglés | IMSEAR | ID: sea-115523

RESUMEN

A case of tetralogy of fallot with congenital intermittent atrioventricular dissociation is reported. A review of standard postgraduate books of cardiology fails to describe this condition, thus showing its extreme rarity. The therapeutic dilemma in treating such a case is also discussed.


Asunto(s)
Niño , Electrocardiografía , Femenino , Bloqueo Cardíaco/congénito , Humanos , Tetralogía de Fallot/complicaciones
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