Genotype-Phenotype Correlation in Indian Patients with MEN2-Associated Pheochromocytoma and Comparison of Clinico-Pathological Attributes with Apparently Sporadic Adrenal Pheochromocytoma.

Sendhil RajanGhazala ZaidiGaurav AgarwalAnjali MishraAmit AgarwalSaroj Kanta MishraEesh Bhatia

Published in: World journal of surgery (2016)

In this cohort of MEN-PCC from India, the commonest causative RET mutations for MEN-PCC involved codon 634. MEN-PCC patients were younger, and more frequently had bilateral PCC than non-MEN disease. MEN-PCC patients in India are diagnosed with large tumors and extremely high catecholamine/metanephrine levels.

Keyphrases

end stage renal disease
middle aged
newly diagnosed
ejection fraction
chronic kidney disease
patient reported outcomes
late onset