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Fig. 3 | BMC Endocrine Disorders

Fig. 3

From: Pheochromocytoma as a rare cause of hypertension in a 46 X, i(X)(q10) turner syndrome: a case report and literature review

Fig. 3

The 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)

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