Pheochromocytoma natural history, complications, and prognosis: Difference between revisions

	Pheochromocytoma Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Pheochromocytoma from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
X Ray
CT
MRI
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Surgery
Primary Prevention
Secondary Prevention
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Pheochromocytoma natural history, complications, and prognosis On the Web
Most recent articles
cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Pheochromocytoma natural history, complications, and prognosis All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Pheochromocytoma natural history, complications, and prognosis
CDC on Pheochromocytoma natural history, complications, and prognosis
Pheochromocytoma natural history, complications, and prognosis in the news
Blogs on Pheochromocytoma natural history, complications, and prognosis
Directions to Hospitals Treating Pheochromocytoma
Risk calculators and risk factors for Pheochromocytoma natural history, complications, and prognosis

Revision as of 15:27, 11 September 2012

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

@@ Line 1: / Line 1: @@
+__NOTOC__
 {{Pheochromocytoma}}
 {{CMG}}
 ==Overview==
+==Natural History==
-A '''pheochromocytoma''' ('''phaeochromocytoma''' outside of the US) is a [[neuroendocrine tumor]] of the [[Adrenal medulla|medulla]] of the [[adrenal gland]]s (originating in the [[chromaffin cell]]s) or extra-adrenal chromaffin tissue which failed to involute after birth,<ref>{{cite book |author=Boulpaep, Emile L.; Boron, Walter F. |title=Medical physiology: a cellular and molecular approach |publisher=Saunders |location=Philadelphia |year=2003 |pages=1065 |isbn=0-7216-3256-4 |oclc= |doi=}}</ref> which secretes excessive amounts of [[catecholamine]]s, usually [[epinephrine]] and [[norepinephrine]].
+==Complications==
-Extra-adrenal [[paragangliomas]] (often described as extra-adrenal pheochromocytomas) are closely related, though less common, tumors that originate in the [[ganglion|ganglia]] of the [[sympathetic nervous system]] and are named based upon the primary anatomical site of origin.
+==Prognosis==
 ==References==
@@ Line 12: / Line 13: @@
 [[Category:Endocrinology]]
 [[Category:Oncology]]
-[[de:Phäochromozytom]]
-[[es:Feocromocitoma]]
-[[fr:Phéochromocytome]]
-[[it:Feocromocitoma]]
-[[he:פאוכרומוציטומה]]
-[[nl:Feochromocytoom]]
-[[ja:褐色細胞腫]]
-[[pl:Guz chromochłonny nadnerczy]]
-[[sv:Feokromocytom]]
 {{WikiDoc Help Menu}}
 {{WikiDoc Sources}}