Inhibin A as a tumor marker for primary bilateral macronodular adrenal hyperplasia

Rachel Wurth1, Crystal Kamilaris1, Naris Nilubol2

  • 1Section on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development.

Summary

Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare cause of Cushing syndrome. Elevated serum inhibin A levels in PBMAH patients suggest its potential as a novel tumor marker for early detection and treatment monitoring.