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Nascer e Crescer
Print version ISSN 0872-0754On-line version ISSN 2183-9417
Abstract
PRETO, Clara et al. Addison’s disease: the difficulty of diagnosis. Nascer e Crescer [online]. 2018, vol.27, n.1, pp.39-42. ISSN 0872-0754.
Introduction: Primary adrenal insufficiency is a rare disease, especially in pediatric age. Case report: We report the case of a teenager with astenia with four months’ evolution, causing repeated visits to the emergency department during the previous month due gastrointestinal symptoms and a ten kilograms weight loss. In admission the patient had a reasonable general condition, hydrated and without cutaneous hyperpigmentation. Laboratory results showed hyponatremia, increased levels of corticotropin with normal cortisol levels, increased levels of renin with decreased aldosterone levels and presence of antissuprarrenal antibodies, allowing the diagnosis of autoimmune primary adrenal insufficiency. The boy started treatment with hydrocortisone and fludrocortisone with favorable response. Discussion/conclusions: The diagnosis of Addison’s disease requires a high degree of suspicion due its unspecific symptomatology. This disease often presents gastrointestinal symptoms. Thus, towards a patient with hyponatremia accompanied by constitutional and gastrointestinal symptoms, we must always consider this diagnosis.
Keywords : Addison’s disease; adrenal insufficiency; autoimmune; gastrointestinal symptoms.