The globally increased blood pressure is the silent killer affecting all age groups hampering the day-to-day lives of people. Pheochromocytomas are a rare cause of secondary hypertension. Pheochromocytoma, with a reported incidence of 2-8 per million, is a rare neuroendocrine tumor originating from the chromaffin cells of the adrenal medulla. It can present with a diverse range of clinical manifestations, often mimicking other conditions, making diagnosis challenging. Surgical resection remains the cornerstone of treatment.
The case of a middle-aged female who presented with a hypertensive
crisis requiring intensive care unit management was presented. Radiological
investigations suggested bilateral pheochromocytoma. A comprehensive diagnostic
workup was performed to confirm the diagnosis before proceeding with bilateral
adrenalectomy. To mitigate the risk of adrenal insufficiency and subsequent
Nelson's syndrome, meticulous postoperative management with mineralocorticoid
and glucocorticoid replacement therapy was implemented.
This case highlights the importance of considering pheochromocytoma
in the differential diagnosis of adrenal masses, the significance of a thorough
preoperative evaluation, and the essential role of postoperative hormonal
replacement therapy in ensuring optimal patient outcomes. The study concluded
that patients with undiagnosed pheochromocytoma may present in extremis to an
emergency department with a pheochromocytoma crisis and coexisting metabolic,
thromboembolic, or surgically emergent events. These patients ultimately
require coordination with complex critical care and optimization for definitive
surgical management, which begins in the emergency department.
Author
(s) Details
Ajinkya
H. Akre
Department of Surgery, Pimpri Chinchwad Municipal Corporations,
Post Graduate Institute, Yashwantrao Chavan Memorial Hospital, Pimpri, Pune,
Maharashtra, India.
Santosh
D. Thorat
Department of Surgery, Pimpri Chinchwad Municipal Corporations,
Post Graduate Institute, Yashwantrao Chavan Memorial Hospital, Pimpri, Pune,
Maharashtra, India.
Please see the book here:- https://doi.org/10.9734/bpi/acmms/v8/3515
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