Secondary arterial hypertension due to pheochromocytoma, complicated by dissecting aortic aneurysm. Review of a clinical case
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Keywords

pheochromocytoma, arterial hypertension, dissecting aortic aneurysm

How to Cite

Solomenchuk, T., Kysil, O., Shavarov, Y., Holub, O., Makhniuk, A., & Gel, K. (2024). Secondary arterial hypertension due to pheochromocytoma, complicated by dissecting aortic aneurysm. Review of a clinical case. The Practitioner, (1), 92-96. Retrieved from https://plr.com.ua/index.php/journal/article/view/807

Abstract

Aim. The article analyzed a rare clinical case of successful treatment of a 44-year-old patient with secondary arterial hypertension caused by a pheochromocytoma of the left adrenal gland complicated by a dissecting aortic aneurysm (DAA). The positive result of the treatment strategy was presented in the article. Results. The diagnosis of chronic DAA according to DeBakey type I was established by multispiral CT angiography of the thoracic and abdominal aorta with intravenous contrast enhancement. An endoprosthetic operation of the descending aorta was performed, followed by a laparoscopic total adrenalectomy on the left side. The patient is under the observation of a cardiologist with the use of pharmacological therapy. Conclusion. Timely diagnosis of severe combined pathology, subsequent surgical correction and drug treatment are aimed at preventing complications and prolonging the patient's life.

pdf (Українська)

References

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