Marzo 2016 - Volume XXXV - numero 3
Pagine elettroniche
1SC di Pediatria d’Urgenza, 2SSVD di Endocrinologia e Diabetologia Pediatrica, AOU Città della Salute e della Scienza di Torino, Ospedale Infantile Regina Margherita, Torino
Indirizzo per corrispondenza: ecastagno@cittadellasalute.to.it
Key words: Addison’s disease, Primary adrenocortical failure, Hyperpigmentation, Hyponatraemia, Hypoglycaemia, Ketosis
Addison’s disease (primary adrenocortical failure) is a rare condition mainly of autoimmune origin. Signs and symptoms are usually mild and non-specific, as abdominal pain, failure to thrive, weight loss, anorexia, vomiting and diarrhoea associated to bronzed skin colour. The diagnosis is often delayed. The paper reports two cases of children in which the association between hyperpigmentation and dehydration with metabolic acidosis, hyponatraemia and hypoglycaemia not proportionate to concomitant vomiting led to the clinical suspect.
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