RESUMO
Originally described in 1955, papular acrodermatitis is considered a rare disease whose manifestations are mainly cutaneous. The disease is characteristically associated to a non icteric hepatitis with B serologic tests positive. We recently observed a case whose etiology is unusual and, therefore, in our opinion worth of a brief description.
Assuntos
Acrodermatite/complicações , Dermatoses da Perna/etiologia , Dermatopatias Vesiculobolhosas/etiologia , Humanos , Lactente , Masculino , SíndromeRESUMO
The authors report the case of a fourteen months old girl who presented with emisomal, uropoietic and vertebral anomalies associated with neurologic handicap. These features can be considered characteristic of facio-auriculo-vertebral spectrum. This syndrome was not frequently described in Italian pediatric literature.
Assuntos
Síndrome de Goldenhar , Disostose Mandibulofacial , Feminino , Síndrome de Goldenhar/diagnóstico , Síndrome de Goldenhar/diagnóstico por imagem , Humanos , Lactente , Disostose Mandibulofacial/diagnóstico , Disostose Mandibulofacial/diagnóstico por imagem , Radiografia , Terminologia como AssuntoRESUMO
A seven years old boy presented with gross hematuria associated with clots and transitory renal insufficiency. The urinary sediment showed only monomorphic red blood cells. Subsequently urinary sediment completely modified: namely only dysmorphic red blood cells and hyaline granular casts were found and within a week renal function become normal. The clinical diagnosis of Berger's disease was possible only with renal biopsy.
Assuntos
Glomerulonefrite por IGA/diagnóstico , Hematúria/etiologia , Biópsia , Criança , Glomerulonefrite por IGA/patologia , Humanos , Rim/patologia , MasculinoRESUMO
The authors report a case of tibial-tarsal septic arthritis caused by a Group A Beta Haemolytic Streptococcus. The primitive pathologic process was an erysipelas with an unusual localization originally of difficult interpretation.