Article Text
Abstract
Cushing’s disease is a rare endocrine condition in which a pituitary corticotroph adenoma drives excess adrenal cortisol production, and is one cause of endogenous Cushing’s syndrome. We present a young woman with 3 weeks of headaches and cognitive disturbance who subsequently developed florid psychosis requiring multiple admissions under neurology and psychiatry. Her clinical stigmata of hypercortisolism and biochemical abnormalities prompted an MR scan of the pituitary, which confirmed a pituitary microadenoma. Treatment with metyrapone and subsequent surgery led to complete recovery within 2 months. Cushing’s disease commonly causes neuropsychiatric symptoms and can present with psychosis. Diagnosing Cushing’s disease can be challenging, but with early diagnosis and treatment it has an excellent prognosis.
- psychosis
- puerperal
- neuroendocrinology
- neurosurgery
Statistics from Altmetric.com
Linked Articles
- Editors’ commentary
Read the full text or download the PDF:
Other content recommended for you
- Cushing's syndrome: a practical approach to diagnosis and differential diagnoses
- Refractory hypokalaemia and hypertension with metabolic alkalosis: an acute presentation of Cushing’s disease secondary to a pituitary macroadenoma
- Clinicopathological correlates of adrenal Cushing's syndrome
- Republished: Clinicopathological correlates of adrenal Cushing's syndrome
- Adrenocortical carcinoma masquerading as Cushing's disease
- Disappearance of pituitary macro adenoma with combination of ketoconazole and cabergoline treatment: an unusual case of Cushing’s syndrome with interesting findings
- Ocular hypertension secondary to high endogenous steroid load in Cushing’s disease
- Use of cabergoline for the management of persistent Cushing’s disease in pregnancy
- Endocrine problems in pregnancy
- Prognostic factors for survival in dogs with pituitary-dependent hypercortisolism treated with trilostane