Name five syndromes that may be encountered with such an adrenal neoplasm?
Multiple endocrine neoplasia syndromes (MEN II and III), von Hippel-Lindau disease, von Recklinghausen neurofibromatosis, Sturge-Weber syndrome and Carney’s triad.
The mass showed low T1 signal intensity, high T2 signal intensity, with no MRI evidence of significantly detectable intracellular (lack of significant signal drop between in-phase and out-of-phase images).