ABSTRACT
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.
Subject(s)
Acrodermatitis/complications , Leg Dermatoses/etiology , Skin Diseases, Vesiculobullous/etiology , Humans , Infant , Male , SyndromeABSTRACT
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.
Subject(s)
Goldenhar Syndrome , Mandibulofacial Dysostosis , Female , Goldenhar Syndrome/diagnosis , Goldenhar Syndrome/diagnostic imaging , Humans , Infant , Mandibulofacial Dysostosis/diagnosis , Mandibulofacial Dysostosis/diagnostic imaging , Radiography , Terminology as TopicABSTRACT
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.
Subject(s)
Glomerulonephritis, IGA/diagnosis , Hematuria/etiology , Biopsy , Child , Glomerulonephritis, IGA/pathology , Humans , Kidney/pathology , MaleABSTRACT
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.