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In this segment, Dr. Kamrun Naher shares why early detection of pheochromocytoma is critical—especially before it causes irreversible cardiovascular complications and renal complications. Though often overlooked, this rare adrenal gland tumor can lead to long-term damage if not recognized in time. Dr. Naher explains how patients typically present with subtle or misattributed pheochromocytoma symptoms such as high blood pressure, chest pain, and palpitations. Many don’t seek help until major organs like the heart or kidneys are already affected. Through improved awareness, better symptom tracking, and early tumor detection, these cases can be caught before lasting harm is done. What you’ll get to know in this video: ▶ How to recognize early signs of adrenal gland disorders and pheochromocytoma pathology ▶ Why pheochromocytoma diagnosis often comes late—and what healthcare professionals should watch for ▶ The importance of genetic counseling for families with a history of adrenal gland tumors ▶ How delays in pheochromocytoma treatment lead to serious cardiovascular disease complications ▶ The role of pheochromocytoma nursing in improving patient care and long-term outcomes ▶ What the medical community—including platforms like pheochromocytoma osmosis—are doing to educate on this rare tumor Early screening and patient education are key to reducing the risk of damage to the adrenal gland, heart, and kidneys—and improving survival rates for those with this rare adrenal tumor. #pheochromocytoma #adrenalglandtumor #earlydetection #cardiovascularcomplications #renalcomplications #pheochromocytomatreatment #geneticcounseling #pheochromocytomasymptoms #pheochromocytomadiagnosis #pheochromocytomanursing #adrenalglanddisorders #highbloodpressure #pheochromocytomaosmosis