Pituitary corticotroph adenoma diagnosis
Pituitary MRI can localize microadenoma in only 50–60% of the cases as the size of the lesion is very small 1).
Although, dynamic studies have improved the sensitivity of MRI, it still fails to localize the adenoma in many cases 2).
High Dose Dexamethasone suppression test (HDDST) has low sensitivity (65%) and specificity (60%) in predicting Cushing's disease 3).
Bilateral inferior petrosal sinus sampling (BIPSS) series has shown the sensitivity of 88–100% and specificity of 67–100% in the localization of the Cushing's disease 4).
The prediction BIPSS of for lateralization of the lesion in Cushing's disease has been questioned, with accuracies ranging from 50% to 100% 5).
Bilateral inferior petrosal sinus sampling (IPSS) with corticotropin-releasing hormone (CRH) is currently the gold standard in the diagnosis of Cushing's disease (CD) and has also been used in tumour lateralization.
To establish a definitive Pituitary corticotroph adenoma diagnosis in the context of pre-existing chronic kidney disease, the absence of circadian rhythms of cortisol and ACTH is a more sensitive indicator than 24-hour urinary free cortisol (24-UFC) and low-dose dexamethasone suppression test 6).