| Literature DB >> 24725972 |
Yoko Morigaki1, Jun-Ichi Iga2, Naomi Kameoka2, Satsuki Sumitani2, Tetsuro Ohmori2.
Abstract
We report a 59-year-old man with isolated adrenocorticotropin (ACTH) deficiency. The patient presented with sudden onset of delusions and hallucinations at the age of 54, which resolved gradually without treatment. Subsequently, the patient manifested stereotypy, wandering, hypobulia, and autistic symptoms, and was treated with antipsychotics for 1 year without any improvement. He suffered from neuroleptic malignant syndrome-like symptoms at the age of 59. A thorough endocrine assessment revealed isolated ACTH deficiency. After hydrocortisone supplementation, the physical and psychiatric symptoms improved dramatically. Clinicians should consider this rare disease when diagnosing patients with refractory psychiatric symptoms and unique physical symptoms of isolated ACTH deficiency.Entities:
Keywords: ACTH deficiency; Depression; Isolated; Neuroleptic malignant syndrome; Organic mental disorders; Psychotic disorders
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Year: 2014 PMID: 24725972 DOI: 10.1016/j.genhosppsych.2014.02.012
Source DB: PubMed Journal: Gen Hosp Psychiatry ISSN: 0163-8343 Impact factor: 3.238