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DOI 10.2147/dmso.s262092

Медицинская библиотека · Diabetes, metabolic syndrome and obesity : targets and therapy · 2020

Adrenal Artery Ablation for the Treatment of Hypercortisolism Based on Adrenal Venous Sampling: A Potential Therapeutic Strategy.

Zhou Qing, Liu Xiaoli, Zhang Hexuan, Zhao Zhigang, Li Qiang, He Hongbo, Zhu Zhiming, Yan Zhencheng

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Аннотация

AIM: Hypercortisolism is characterized by metabolic disorders and high mortality rates. Adrenalectomy and medical therapies are considered major treatment options. However, some patients, especially young patients, are strongly against undergoing surgery in case of secondary hypocortisolism or relapses that require replacement supplements or pharmacological interventions. In such cases, alternative therapies are needed to treat hypercortisolism.

METHODS

We report a 27-year-old Chinese female with adrenal cortisol-producing adenoma. The patient's circadian rhythm and concentrations of cortisol were abnormal, accompanying with an increased 24-hour urinary cortisol level. Computed tomography (CT) revealed a nodular soft-tissue mass in the right adrenal gland.

RESULTS

Cortisol hypersecretion from the right adrenal gland was verified by adrenal venous sampling (AVS). Adrenal artery ablation was performed. After ablation, long-term follow-up showed that the patient's symptoms subsided and abnormal laboratory test results returned to normal without pharmacological treatment.

CONCLUSION

AVS might be a promising method to aid the diagnosis of cortisol-producing adenoma. Adrenal artery ablation is minimally invasive and may be useful for the treatment of adrenal adenoma or nodular diseases, especially in patients who cannot undergo surgery.

Для цитирования: Zhou Qing, Liu Xiaoli, Zhang Hexuan, Zhao Zhigang, Li Qiang, He Hongbo, Zhu Zhiming, Yan Zhencheng. Adrenal Artery Ablation for the Treatment of Hypercortisolism Based on Adrenal Venous Sampling: A Potential Therapeutic Strategy.. Diabetes, metabolic syndrome and obesity : targets and therapy. 2020. DOI: 10.2147/dmso.s262092.
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