Asunto(s)
Convalecencia , Dengue/diagnóstico , Exantema/virología , Fiebre/virología , Niño , Femenino , Humanos , Lactante , MasculinoRESUMEN
Drug-related dystonic reactions are not uncommon and often misdiagnosed as encephalitis, seizures, tetanus, tetany, etc. Eliciting thorough history is important to avoid unnecessary investigations and treatments as these are potentially reversible reactions. Metoclopramide-induced oculogyric crisis is described in this case report.
RESUMEN
The association between hypertensive encephalopathy and cortical blindness in children with acute glomerulonephritis is extremely rare. We report the case of a 9-year old girl who presented with headache, seizures, altered sensorium, hematuria, and transient cortical blindness as a complication of hypertensive encephalopathy which showed complete reversal following normalization of blood pressure and an underlying post-infectious acute glomerulonephritis was revealed.
Asunto(s)
Calcinosis/diagnóstico por imagen , Hipocalcemia/diagnóstico por imagen , Brazo/diagnóstico por imagen , Brazo/patología , Calcinosis/inducido químicamente , Calcinosis/patología , Calcio/efectos adversos , Calcio/uso terapéutico , Gluconato de Calcio/efectos adversos , Gluconato de Calcio/uso terapéutico , Humanos , Hipocalcemia/tratamiento farmacológico , Enfermedad Iatrogénica , Recién Nacido , Masculino , RadiografíaAsunto(s)
Fallo Hepático Agudo/virología , Dengue Grave/complicaciones , Humanos , Lactante , MasculinoAsunto(s)
Labio/patología , Síndrome de Melkersson-Rosenthal/patología , Antiinflamatorios no Esteroideos/uso terapéutico , Niño , Clofazimina/uso terapéutico , Humanos , Masculino , Síndrome de Melkersson-Rosenthal/diagnóstico , Síndrome de Melkersson-Rosenthal/tratamiento farmacológico , Esteroides/uso terapéuticoRESUMEN
Systemic lupus erythematosus (SLE) is an episodic, potentially fatal, multisystem autoimmune disease characterized by the presence of antinuclear antibodies especially to double stranded DNA. Bullous systemic lupus erythematosus is an extremely rare subset of lupus erythematosus. We report a 10-year-old boy with bullous SLE and nephrotic syndrome.