RESUMEN
Introduction: The systemic juvenile scleroderma [SJS] is a rare acquired auto-immune disease. The aim of our study was to analyse the epidemiologic, clinical, therapeutic and prognostic features
Patients and Methods: through a retrospective study, 6 patients were observed with SJS. We adopted the Barnett's classification. Results: The six patients were females, with a mean age of began on 9 +/- 3 years. Five patients were classified type II of Barnett and for 1 patient the classification was difficult. Raynaud's phenomen was observed in 4 cases. The cutaneous sclerosis was noted in the all cases. Five children presented oesophageal damage. Lung involvement was noted in 3 cases. No cardiac dysfunction was found at the clinical exam. Mild renal involvement was noted in 1 case. SJS was associated to systemic lupus in 2 cases and to dermatomyositis in 1 case
Discussion: Systemic juvenile scleroderma is rare. The cardiac involvement is a major concern in children; it appears to be a more common cause of death in SJS. The therapeutic problems were similar to those in adults
RESUMEN
Impetigo is a superficial non follicular pyoderma due mainly to staphylococcus aureus and/or to streptococcus pyogenes. It occurs chiefly in childhood. We achieved a retrospective study dealing with 93 cases of impetigo occurring in childhood. The aim of this study was to evaluate the epidemiological and clinical features of this condition and its management. In our series, the mean age was 4.5 years with no sex predominance. Thirteen patients [14 per cent] had chronic diseases. Atopic dermatitis was seen in only 6.5 per cent of our patients. Impetigo occurred mainly in summer and autumn. The lesions were mostly erosions covered with yellowish crusts. Rarely, it was matter of vesicles and blisters. These lesions were mainly localized on the face. Treatment was based on antiseptic agents in all patients, associated to topical or systemic antibiotics