Severe Paroxysmal Hypertension (Pseudopheochromocytoma) Case Report
International Journal of Development Research
Severe Paroxysmal Hypertension (Pseudopheochromocytoma) Case Report
Received 11th October, 2025; Received in revised form 09th November, 2025; Accepted 20th December, 2025; Published online 30th January, 2026
Copyright©2026, Dr. Jimit Patel and Dr. N. D. Khimesra. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Paroxysmal hypertension is characterized by sudden, episodic elevations in blood pressure accompanied by autonomic symptoms such as headache, palpitations, and diaphoresis. These episodes may closely mimic pheochromocytoma, making diagnosis challenging when biochemical and imaging studies are negative. We present a case of severe paroxysmal hypertension in a middle-aged male who experienced recurrent hypertensive crises with normal inter-episodic blood pressure. This case highlights the importance of recognizing pseudopheochromocytoma as a distinct clinical entity and outlines an effective management strategy.