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Reversible dilated cardiomyopathy as a complication of adrenal cortex insufficiency: a case report
Mohammad Alkhateeb1, Mohammad Alsakkal2, Mohammad Nour Alfauri2
1Damascus University - Faculty of Medicine, Damascus, Syria. moh-alkh-123@hotmail.com.
Insights
Addison's disease can lead to dilated cardiomyopathy in children. Glucocorticoid therapy effectively reversed cardiac dysfunction in a pediatric case, highlighting a rare but treatable complication of primary adrenal insufficiency.
Area of Science:
- Pediatric Cardiology
- Endocrinology
- Rare Diseases
Background:
- Cardiovascular complications are known in Addison's disease.
- Primary adrenal insufficiency (Addison's disease) can present with varied symptoms.
- Autoimmune causes are the most common etiology for primary adrenal insufficiency.
Observation:
- An 11-year-old girl presented with symptoms suggestive of primary adrenal insufficiency.
- Diagnostic workup revealed dilated cardiomyopathy.
- Other causes of primary adrenal insufficiency were ruled out.
Findings:
- Dilated cardiomyopathy is a rare complication of primary adrenal insufficiency.
- Glucocorticoid replacement therapy led to significant recovery of cardiac function.
- This is the first reported case in Syria.
Implications:
- Early diagnosis and treatment of adrenal insufficiency are crucial.
- Reversible cardiomyopathy can occur as a complication of primary adrenal insufficiency.
- This case underscores the importance of cardiac monitoring in pediatric patients with Addison's disease.
Background:
Cardiovascular manifestations associated with Addison's disease are previously documented. We described a case of an 11-year-old girl who developed dilated cardiomyopathy as a complication to Addison's disease. Glucocorticoid replacement therapy resulted in near-complete recovery of cardiac function. It is the first reported case of reversible cardiomyopathy as a complication of primary adrenal insufficiency in Syria.
Case Presentation:
An 11-year-old Caucasian girl with no significant past medical history presented with abdominal pain, vomiting after meals, and a low-grade fever. A physical examination and laboratory evaluation suggested primary adrenal insufficiency. An echocardiogram showed changes consistent with dilated cardiomyopathy. Causes of primary adrenal insufficiency other than autoimmune were excluded.
Conclusions:
Dilated cardiomyopathy is a rare complication of primary adrenal insufficiency. Proper treatment of adrenal insufficiency with glucocorticoid replacement therapy resulted in restoration of normal cardiac function.
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