Fig. 3From: Pheochromocytoma as a rare cause of hypertension in a 46 X, i(X)(q10) turner syndrome: a case report and literature reviewThe cut surface of the tumour was tan and darkened, with focal haemorrhage and extended to the adrenal cortex but was well-circumscribed (a). The tumour showed characteristic “Zellballen” architecture and tumor cells were larger than normal chromaffin cells, and their cytoplasm was granular (b). Immunostaining for S-100 protein demonstrate the sustentacular framework surrounding the tumor cells (c) and positive for chromogranin (d)Back to article page