Abstract
Compared with the general population, rates of pheochromocytoma are higher in neurofibromatosis type 1 (NF1) patients. However, pheochromocytoma testing is often plagued by false positive results. Here we present a patient with NF1, elevated urinary metanephrine levels, and an indeterminate adrenal nodule. Clonidine suppression testing aided diagnosis and led to definitive surgical treatment that confirmed a pheochromocytoma. Pheochromocytoma screening and clonidine suppression testing can both aid in the evaluation for catecholamine-secreting tumours.
| Original language | English |
|---|---|
| Article number | e228263 |
| Journal | BMJ Case Reports |
| Volume | 12 |
| Issue number | 6 |
| DOIs | |
| State | Published - 1 Jun 2019 |
Keywords
- Adrenal disorders
- Neuro genetics