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Addison's disease due to tuberculosis that required differentiation from SIADH
Takeshi Kinjo1, Daisuke Higuchi, Yasuji Oshiro
1Department of Respiratory Medicine, National Hospital Organization Okinawa Hospital, Okinawa, Japan. kumanomis6@yahoo.co.jp
Summary
This case study highlights a patient initially suspected of SIADH due to tuberculosis, but ultimately diagnosed with Addison's disease. Early diagnosis and hydrocortisone treatment are crucial for managing adrenal insufficiency in tuberculosis patients.
Area of Science:
- Endocrinology
- Infectious Diseases
- Radiology
Background:
- Hyponatremia can be a presenting symptom of various conditions, including endocrine disorders and infections.
- Tuberculosis can affect multiple organs, including the adrenal glands, potentially leading to adrenal insufficiency.
- Syndrome of Inappropriate Antidiuretic Hormone secretion (SIADH) is a common cause of hyponatremia, often associated with malignancies or infections.
Observation:
- A 77-year-old male presented with fatigue and severe hyponatremia (serum sodium 116 mEq/l).
- FDG-PET imaging suggested SIADH secondary to extrapulmonary tuberculosis, with brain and adrenal nodules observed.
- The patient's condition deteriorated upon initiation of anti-tuberculosis therapy.
Findings:
- Hormonal tests confirmed Addison's disease as the underlying cause of hyponatremia.
- High-dose hydrocortisone administration led to immediate clinical improvement.
- Anti-tuberculosis medications resulted in the reduction of tuberculous lesions.
Implications:
- Adrenal insufficiency, specifically tuberculous Addison's disease, should be considered in patients with hyponatremia and active or past tuberculosis.
- Prompt diagnosis and appropriate management, including corticosteroid replacement, are vital for patient recovery.
- Despite decreasing incidence, vigilance for tuberculous Addison's disease remains important in clinical practice.
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