Adrenal pheochromocytoma (with probable underlying MEN IIa
The 20-year-old female patient initially with a history of thyroid cancer underwent thyroidectomy 1 year ago presenting with hypertension. The abdominal US suggested an adrenal mass.CT was done for further evaluation.
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Right adrenal well defined ovoid mass is seen showing heterogeneous enhancement with areas of hypodense attenuation of breaking down within.
The patient was operated and pathologically proven pheochromocytoma.
In the setting of the cancer thyroid and pheochromocytoma, MEN IIa is most likely.