ArticleBMC research notes2014
Recurrent hypoglycaemia in type-1 diabetes mellitus may unravel the association with Addison's disease: a case report.
Article in BMC research notes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Schmidt's Syndrome: An Uncommon Cause of Spontaneous Hypoglycemia.Avicenna journal of medicine · 2024Article
- The multiple faces of autoimmune Addison's disease in children.Frontiers in endocrinology · 2024Review
- Adolescent onset of autoimmune polyglandular syndrome type 2.BMJ case reports · 2022Article
- Type 1 Diabetes and Addison's Disease: When the Diagnosis Is Suggested by the Continuous Glucose Monitoring System.Children (Basel, Switzerland) · 2021Article
- Novel presentation of autoimmune polyglandular syndrome II in a child with simultaneous Addison's disease, type 1 diabetes, and Hashimoto's thyroiditis: A case report.Clinical case reports · 2021Article
- Mixed phenotypic presentation of autoimmune polyendocrine syndrome type II in adolescent female.Journal of family medicine and primary care · 2020Article
- A Rare Case of Autoimmune Polyglandular Syndrome Type 2 in a Child With Persistent Fatigue.Global pediatric health · 2019Article
- Commentary: Early Clinical Indicators of Addison's Disease in Adults With Type 1 Diabetes: A Nationwide, Observational, Cohort Study.Frontiers in endocrinology · 2019Article
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4 authors.
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Abstract
backgroundPrimary adrenocortical insufficiency or Addison's disease is caused by a progressive destruction of the adrenal cortex, resulting into a reduction of glucocorticoids, mineralocorticoids, and androgens. Autoimmune Addison's disease is the most common etiological form, accounting for about 80% of all cases. CASE PRESENTATION: We describe the case of a 16-year-old Caucasian boy affected by type-1 diabetes mellitus and autoimmune thyroiditis, who experienced recurrent hypoglycaemia as presenting symptom of Addison's disease.
conclusionsHypoglycaemia is not a common presenting feature of Addison's disease, both in patients with type-1 diabetes mellitus and in non-diabetic patients. However, hypoglycaemia may occur in association with primary and secondary glucocorticoid deficiency as a result of an enhanced insulin sensitivity. Hypoglycaemia is the most common acute complication of insulin therapy in patients with type-1 diabetes mellitus. Addison's disease has been described in approximately 0.5% of patients with type-1 diabetes mellitus, being more frequent in females and occurring in middle-aged patients. An association among type-1 diabetes mellitus, autoimmune thyroiditis, and Addison's disease is found in the "Schmidt's syndrome", a rare disorder that may occur in the paediatric age. Our case suggests that the presence of Addison's disease should be taken into consideration in patients with type-1 diabetes mellitus and frequent episodes of hypoglycaemia. We wish to highlight that there are no specific indications to screen for the association between Addison's disease and type-1 diabetes mellitus, although an early diagnosis of Addison's disease in diabetic patients would prevent the morbidity and potential mortality of this association.
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