Abstract
A phaeochromocytoma is a rare catecholamine-secreting tumour arising from the chromaffin cells. We describe a case of a child with Von Hippel-Lindau disease, with an adrenal phaeochromocytoma who presented with severe dilated cardiomyopathy driven by secondary hypertension. Contrast-enhanced ultrasound findings are described and compared with both magnetic resonance imaging and computed tomography imaging.
| Original language | English |
|---|---|
| Pages (from-to) | 307-311 |
| Number of pages | 5 |
| Journal | Journal of Ultrasound |
| Volume | 17 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 14 Dec 2014 |
| Externally published | Yes |
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