PPT-Pheochromocytoma

Dr Atallah Al Ruhaily Pheochromocytoma Catecholamine PhysiologyPathophysiology Clinical Presentation Epidemiology Signs amp Symptoms Diagnosis Biochemical Localization Management Preoperative. Sona Sharma MD. Associate Professor of Clinical Medicine. Division of Endocrinology, Diabetes and Metabolism. University . of Cincinnati College of Medicine. February 2018 . Southwest Ohio Regional Updates . Matt Jepson, DO Intern Case Report E.A. is a 44 F CC: Chest pain, shortness of breath HPI: Constant, 7/10, sharp pain at xiphoid process radiating straight to her back Started suddenly at 02:00, worsened by movement, improved with lying down Acu. ), . Dip. . Diab.DCA. , Dip. Software statistics- . Phd. Mahatma Gandhi Medical college and research institute , . puducherry. , India. . Anaesthetic. management . o. f . pheochromocytoma. . Management of Hormonal Manifestations. Camilo Jimenez Vasquez. Professor. Department of Endocrine Neoplasia and Hormonal Disorders . The University of Texas MD Anderson Cancer Center. Outline. Introduction. Bita. . Mirzaei. MD. Endocrinology Fellow. Research Institute for Endocrine sciences. Shahid. . Beheshti. University of Medical Sciences . Mordad. 94. . Silent . pheochrmocytoma. ?. Familial . pheochromocytoma. Irina Bancos. Associate Professor. Endocrinology. Mayo Clinic, Rochester, Minnesota. Disclosure . Nothing to disclose in relation to current presentation. Other disclosures: advisory board, consulting, data safety board for . neurofibromatosis: neurofibromatosis . types 1 and 2 (. NF1. and . NF2. ) and . schwannomatosis. Neurofibromatosis (NF) is a genetic neurological disorder that can affect the brain, spinal cord, nerves and skin. GROUP ONE. AMADI. , VERA HOMA (PRESENTER) 15/MHS06/014. ALABADAN OYEBOLA 15/MHS06/012. CHINKERE CHIAMAKA 15/MHS06/020. Normal parathyroid. Incidental cyst. (not important). capsule. The neoplasm. Normal parathyroid. Parathyroid adenoma. Tumor behavior is . much more important . than morphology. Tumor invasion in the capsule. Dieter Nürnberg (corresponding author), Agnes SzebeniFrantišek ZáOlomouc, Czech Republic Corresponding author: Ruppiner Kliniken GmbH Department of Internal Medicine . Ultrasound of the adrena Al-. Ruhaily. Pheochromocytoma. Catecholamine Physiology/Pathophysiology. Clinical Presentation. Epidemiology. Signs & Symptoms. Diagnosis. Biochemical. Localization. Management. Preoperative. Operative. Content. Headache. Giddiness. Loss of Consciousness. Weakness/Lethargy. Headache. Approach. Primary vs Secondary. Red Flags. Patterns: Raised ICP features, thunderclap, visual disturbances, hypertension. Adrenal Physiology Review . Synthesis of AC Steroid Hormones. Backbone: 21-carbon steroid. GCs: Ketone C3, OH C11/C21. MC: Double bond O C18. Androgens: Double bond O C17. 19 Carbon Steroid. AC Biosynthetic Pathways. Pheochromocytoma. Uncommon tumor of the chromaffin cells in the adrenal medulla. Occasionally can arise from chromaffin cells outside the adrenal gland. Right adrenal more common than left. Bilateral has been reported.