Abstract
Investigating a recently developed Cushing Syndrome, we diagnosed in a 47-year-old woman an ectopic ACTH syndrome due to a metastatic carcinoid tumor, most likely a thymic carcinoid tumor. Combined therapy with sandostatin and nizoral and later on with sandostatin, metopirone and orimeten, was not able to suppress the hypercortisolism. A few weeks after surgical adrenalectomy, clinical deterioration ensued, culminating in the patient's death 7 months after diagnosis.
Original language | English |
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Pages (from-to) | 23-25 |
Number of pages | 3 |
Journal | Acta clinica Belgica |
Volume | 57(1) |
Issue number | 1 |
Publication status | Published - Jan 2002 |
ASJC Scopus subject areas
- General Medicine