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TITLE:

CASE STUDY ON PHEOCHROMOCYTOMA

AUTHORS:

Sadia Hassan, Mr. Muhammad Afzal, Ms. Hajra Sarwar

ABSTRACT:

Pheochromocytoma is unusual catecholamine emit tumor start typically from adrenal medulla and maker sign and symptoms proper to acute catecholamine release from tumor. A 20 years old young man was admitted in Public Hospital with complaint of raging attack of palpitations, faintness, Fever from previous 15 days and nausea from 3 days, History of weight loss(10kg) and sleep distraction. Clinical idea of chromaffin cell tumor is well-known by twenty four hours epinephrine level, abdominal Ultrasound and Computerized tomography scan. Surgical removal of pheochromocytoma was done after two weeks of preoperative arrangements. Preoperative variation of Blood Pressure was well organized by Intravenous fluid, small and ephedrine. From First post operative day Blood pressure regains to normal range. Paraganglioma is a rare reason of hyperpiesia. Whether, the identification of this tumor is dominate ,the outcome could be tragic, even deadly;though,if it is recognize, has chances to be cured,as being one of the reason of surgically improveable high blood pressure. (Neuman, Pawlu & Peczkowska, 2014).

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