Ependymoma pathophysiology: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
Line 7: Line 7:
==Pathophysiology==
==Pathophysiology==


*Ependymomas represent a relatively broad group of glial tumours which share common origin from differentiated ependymal cells lining the ventricles of the brain or the central canal of the spinal cord. They account for ~5% of all neuroepithelial neoplasms, ~10% of all paediatric brain tumours and up to 33% of brain tumours occurring in those less than 3 years of age.
*Ependymomas can occur anywhere, but certain location are typical. Common locations include:
:*Floor of the fourth ventricle (common location in children)
:*Spinal cord ependymoma
:*Myxopapillary ependymoma (conus medullaris)
:*Supratentorial ependymoma
*The subependymomas, variant of the ependymoma, arise in the fourth ventricle but may occur in the [[septum pellucidum]] and the cervical spinal cord.
===Gross Pathology===
===Gross Pathology===
*Ependymomas develop from cells that line the [[brain]] ventricles and [[spinal canal]].
*Ependymomas are well-encapsulated tumors and usually arise from the floor of the [[fourth ventricle]], situated in the lower back portion of the brain.
*They are well-encapsulated tumors and usually arise from the floor of the [[fourth ventricle]], situated in the lower back portion of the brain.
 
*The subependymomas, variant of the ependymoma, arise in the fourth ventricle but may occur in the [[septum pellucidum]] and the cervical spinal cord.


===Microscopic Pathology===
===Microscopic Pathology===

Revision as of 15:06, 6 October 2015

Ependymoma Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Epidemiology and Demographics

Risk Factors

Differentiating Ependymoma from other Diseases

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Staging

Laboratory Findings

CT

MRI

Ultrasound

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

Ependymoma pathophysiology On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Ependymoma pathophysiology

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Ependymoma pathophysiology

CDC on Ependymoma pathophysiology

Ependymoma pathophysiology in the news

Blogs on Ependymoma pathophysiology

Directions to Hospitals Treating Ependymoma

Risk calculators and risk factors for Ependymoma pathophysiology

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]

Overview

Pathophysiology

  • Ependymomas represent a relatively broad group of glial tumours which share common origin from differentiated ependymal cells lining the ventricles of the brain or the central canal of the spinal cord. They account for ~5% of all neuroepithelial neoplasms, ~10% of all paediatric brain tumours and up to 33% of brain tumours occurring in those less than 3 years of age.
  • Ependymomas can occur anywhere, but certain location are typical. Common locations include:
  • Floor of the fourth ventricle (common location in children)
  • Spinal cord ependymoma
  • Myxopapillary ependymoma (conus medullaris)
  • Supratentorial ependymoma
  • The subependymomas, variant of the ependymoma, arise in the fourth ventricle but may occur in the septum pellucidum and the cervical spinal cord.

Gross Pathology

  • Ependymomas are well-encapsulated tumors and usually arise from the floor of the fourth ventricle, situated in the lower back portion of the brain.


Microscopic Pathology

Ependymomas are composed of cells with regular, round to oval nuclei. There is a variably dense fibrillary background. Tumor cells may form gland-like round or elongated structures that resemble the embryologic ependymal canal, with long, delicate processes extending into the lumen; more frequently present are perivascular pseudorosettes in which tumor cells are arranged around vessels with an intervening zone consisting of thin ependymal processes directed toward the wall of the vessel.[1]. Ependymal rosettes are rare but pathognomonic feature.

Micrograph of an ependymoma
True ependymal rosette consisting of tumor cells arranged around well-defined lumens forming gland-like structures.


Associated Conditions

The subependymal giant-cell astrocytoma, also called giant-cell glioma, is typically associated with tuberous sclerosis but can occur independent of that condition.

References

  1. Kumar, et al. (2005). The Central Nervous System. Pathologic Basis of Disease. 7th Edition. Philadelphia: Elsevier Saunders.

Template:WikiDoc Sources