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Updated: Jan 9, 2026

A Novel Method: Super-selective Adrenal Venous Sampling
Published on: September 15, 2017
Diagnostic Challenges of Adrenal Venous Sampling for Primary Hyperaldosteronism in a Patient With Subclinical
Mahsa Malekian1, Vahide Sadra1, Amir Bahrami1
1Endocrine Research Center Tabriz University of Medical Sciences Tabriz Iran.
Insights
Secondary hypertension, often caused by adrenal gland disease, is rising. This case highlights primary hyperaldosteronism and mild autonomous hypercortisolism, emphasizing the need for thorough adrenal evaluation in hypertensive patients.
Area of Science:
- Endocrinology
- Nephrology
- Internal Medicine
Background:
- Hypertension is a prevalent comorbidity, with secondary hypertension accounting for 5%-10% of cases.
- Adrenal gland diseases are common causes of secondary hypertension, necessitating accurate diagnosis and management.
- This case presents a complex scenario involving uncontrolled hypertension, primary hyperaldosteronism, and mild autonomous hypercortisolism.
Purpose of the Study:
- To investigate the diagnostic challenges in a patient with uncontrolled hypertension and suspected adrenal gland pathology.
- To evaluate the utility of imaging and biochemical tests in differentiating adrenal adenoma from adrenal hyperplasia.
- To highlight the importance of comprehensive hormonal evaluation in hypertensive patients with adrenal incidentalomas.
Main Methods:
- Biochemical assays including electrolytes, renin, aldosterone, cortisol, and ACTH levels were performed.
- Abdominal computed tomography (CT) was used to identify adrenal masses.
- Adrenal vein sampling and the 1mg overnight dexamethasone suppression test were conducted for further diagnostic clarification.
Main Results:
- Laboratory findings were consistent with primary hyperaldosteronism (PHA).
- CT revealed an adrenal mass, but adrenal vein sampling suggested adrenal hyperplasia.
- The dexamethasone suppression test indicated mild autonomous hypercortisolism.
Conclusions:
- Computed tomography (CT) has limitations in differentiating adrenal adenomas from bilateral idiopathic adrenal hyperplasia.
- Patients aged 35 and older with adrenal incidentalomas require thorough evaluation for PHA, even with visible masses on CT.
- Comprehensive hormonal assessment is crucial for accurate diagnosis and management of secondary hypertension due to adrenal disorders.
Abstract:
Hypertension is a significant comorbidity in the New World, and its prevalence is rising. Around 5%-10% of cases with hypertension have secondary hypertension. Adrenal gland disease is among the common causes of secondary hypertension. We present a 57-year-old male with uncontrolled hypertension and a history of intracranial hemorrhage. The lab evaluation of the patient revealed a K+ of 3.8 mEq/L, Na + of 138 mEq/L, Renin of 2.6 mIU/L, Aldosterone of 47.3 ng/dL, consistent with primary hyperaldosteronism (PHA). The patient's abdominal computed tomography (CT) revealed an adrenal mass measuring 21 mm in the right adrenal gland. However, the adrenal-vein sampling showed that the mass is probably not the source of aldosterone excess, and a possible diagnosis of adrenal hyperplasia was made. To investigate the adrenal incidentaloma, the 1 mg overnight dexamethasone suppression test was performed. The 8 a.m. cortisol and ACTH levels were reported to be 5 microg/dL and 3.2 pg/mL, and a diagnosis of mild autonomous hypercortisolism was also made. CT is not an accurate method to differentiate between an adrenal-producing adenoma and bilateral idiopathic adrenal hyperplasia. Even in cases where a visible mass is detected on CT, patients aged 35 or older need to be evaluated for the cause of PHA.
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