Abstract
Cushing syndrome as the presenting symptom of a malignant renal tumor in children is rare. We report the first case of paraneoplastic Cushing syndrome due to a Wilms tumor, in which clinical and biological signs of hypercortisolism regressed during preoperative chemotherapy. Additionally, we reviewed the literature on paraneoplastic Cushing syndrome secondary to pediatric renal tumors.
Original language | English |
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Pages (from-to) | 211-213 |
Number of pages | 3 |
Journal | Pediatric Blood and Cancer |
Volume | 53 |
Issue number | 2 |
DOIs | |
Publication status | Published - 1 Aug 2009 |
Keywords
- Adrenocorticotropic hormone (ACTH)
- Corticotrophin-releasing hormone (CRH)
- Cushing syndrome
- Nephroblastoma
- Renal tumor