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.
Sommario
Il feocromocitoma è un tumore secernente catecolamine, raro; deriva dalle cellule cromaffini. Descriviamo il caso di un bambino con malattia di Von Hippel-Lindau, con feocromocitoma surrenale che si è presentato con grave cardiomiopatia dilatativa causata da ipertensione secondaria. Vengono descritte le caratteristiche ecografiche con mezzo di contrasto, comparate sia a risonanza magnetica che a tomografia computerizzata.
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Conflict of interest
Faise Al Bunni, Annamaria Deganello, Maria E. Sellars, Klaus-Martin Schulte Mudher Al Adnani, Paul S. Sidhu declare that they have no conflict of interest related to this paper.
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All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000 (5). All patients provided written informed consent to the publication of this paper and to the inclusion in this article of information that could potentially lead to their identification.
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Al Bunni, F., Deganello, A., Sellars, M.E. et al. Contrast-enhanced ultrasound (CEUS) appearances of an adrenal phaeochromocytoma in a child with Von Hippel-Lindau disease. J Ultrasound 17, 307–311 (2014). https://doi.org/10.1007/s40477-014-0083-8
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DOI: https://doi.org/10.1007/s40477-014-0083-8