Abstract

Background. Hypothyroidism is a prevalent endocrine disorder, often presenting with a spectrum of symptoms reflecting a hypothyroid state. It is also generally linked to causing mood swings, psychomotor slowing, and fatigue; however, in rare instances, it may lead to or induce acute psychosis, a condition referred to as myxedema psychosis (MP). We report a case of myxedema psychosis and present a literature review discussing its presentation, diagnosis, management, and prognosis. Case Presentation. A 36-year-old lady presented with one-week history of persecutory and paranoid delusions, along with visual and auditory hallucinations. She had no prior history of psychiatric illnesses. She underwent total thyroidectomy three years before the current presentation due to papillary thyroid cancer. She was not on regular follow-up, nor any specific therapy. On examination, she was agitated and violent. There were no signs of myxedema, and the physical exam was unremarkable. The initial workup showed a mild elevation in serum creatinine. Additional investigations revealed a high thyroid-stimulating hormone (TSH) of 56.6 mIU/L, low free T4 < 0.5 pmol/L, elevated creatine kinase of 3601 U/L, and urine dipstick positive for blood, suggestive of myoglobinuria. MRI of the head was unremarkable. We diagnosed her as a case of myxedema psychosis and mild rhabdomyolysis. She was started on oral thyroxine 100 mcg/day, fluoxetine 20 mg daily, and as-needed haloperidol. She was closely followed and later transferred to the Psychiatry Hospital for further management. Within one week, her symptoms improved completely, and she was discharged off antipsychotics with additional scheduled follow-ups to monitor TFTs and observe for any recurrence. Discussion and Conclusion. Myxedema psychosis is a rare presentation of hypothyroidism—a common endocrine disorder. Scarce data are describing this entity; hence, there is currently a lack of awareness amongst clinicians regarding proper identification and management. Moreover, the atypical nature of presentations occasionally adds to a diagnostic dilemma. Thus, any patient with new-onset psychosis should be screened for hypothyroidism, and awareness of this entity must be emphasized amongst clinicians and guideline makers.

Highlights

  • Hypothyroidism is a prevalent endocrine disorder, often presenting with a spectrum of symptoms reflecting a hypothyroid state

  • We report the case of a young lady with myxedema psychosis and present a summary of an updated literature review with the hope of providing clinicians with a useful guide to better identify and treat this condition

  • The patient returned to her home country, and she was lost to follow-up thereafter; information regarding medication compliance, adverse effects, or any further relapses of myxedema psychosis is not available

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Summary

Background

When psychosis occurs as a result of a medical condition or drug, it is called secondary psychosis [1]. Amongst a variety of medical conditions, hypothyroidism can rarely lead to psychosis. This relationship was explored in 1949 by Professor Asher, and at the time, the term “myxedema madness” was coined [2]. The term myxedema psychosis (MP) is emerging as it better describes the condition [3, 4]. Given the rarity of the disorder, there is a significant gap in knowledge and awareness about the presentation, diagnosis, and treatment of this condition. We report the case of a young lady with myxedema psychosis and present a summary of an updated literature review with the hope of providing clinicians with a useful guide to better identify and treat this condition

Case Presentation
Discussion
Conclusion
Conflicts of Interest

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