【 摘 要 】
Myxoedema madness was first described as a consequence of severe hypothyroidism in 1949. Most cases were secondary tolong-standing untreated primary hypothyroidism. We present the first reported case of iatrogenic myxoedema madnessfollowing radioactive iodine ablation for Graves’ disease, with a second concurrent diagnosis of primary hyperaldosteronism.A 29-year-old woman presented with severe hypothyroidism, a 1-week history of psychotic behaviour and paranoid delusions3 months after treatment with radioactive iodine ablation for Graves’ disease. Her psychiatric symptoms abated withlevothyroxine replacement. She was concurrently found to be hypertensive and hypokalemic. Primary hyperaldosteronismfrom bilateral adrenal hyperplasia was diagnosed. This case report serves as a reminder that myxoedema madness can be acomplication of acute hypothyroidism following radioactive iodine ablation of Graves’ disease and that primaryhyperaldosteronism may be associated with autoimmune hyperthyroidism.
【 授权许可】
CC BY-NC-ND
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202303290004448ZK.pdf | 123KB |
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