Optic nerve glioma surgery: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
Line 1: Line 1:
__NOTOC__
__NOTOC__
{{CMG}}
{{CMG}}{{AE}}{{Simrat}}
{{Optic nerve glioma}}
{{Optic nerve glioma}}
==Overview==
==Overview==
Treatment varies with the size of the tumor and the general health of the person. The goal may be to cure the disorder, relieve symptoms, or improve vision and comfort.
Surgery is not the first-line treatment option for patients with optic nerve glioma. Surgical excision is usually reserved for patients with either progressive proptosis, blindness, exophytic chiasm tumor causing mass effect, hydrocephalus, or with increased intracranial pressure.
==Surgery==
==Surgery==
Surgical removal may cure some optic gliomas. Partial removal to reduce the bulk of the tumor can be done in many cases. This will keep the tumor from damaging normal brain tissue around the tumor.
*Usually surgery is not preferred for this type of tumor, but it can sometimes improve vision and/or relieve symptoms.
===Radiation therapy===
*If the glioma causes an increase in intracranial pressure, excision may be required.
Radiation therapy may be advised in some cases where the tumor is larger and surgery is not possible. In some cases, radiation therapy may be delayed because of the slow growth that this tumor typically displays.
*Where there is residual vision, excision is rarely utilized.
*Surgical treatment for optic pathway gliomas usually involves either excision or biopsy of the tumor.  
*Surgery is the first choice when single nerve involvement is causing either progressive disfiguring proptosis, blindness, or an exophytic chiasm tumor is causing mass effect or hydrocephalus.
*Biopsy is associated with some risk, and is not usually recommended for chiasmatic lesions involving visual pathway.
*Diffuse infiltration of the chiasm is a contraindication to surgery.
*Due to damage the risk of visual loss as well as damage to surrounding neurologic structures, surgical intervention for gliomas involving the optic chiasm is considered only for obtaining a biopsy specimen of the chiasm in certain cases or for relieving hydrocephalus.
*NF-1 patients have increased risk of local recurrence after surgery than non-NF patients and tend to have less localized disease.


==References==
==References==

Revision as of 00:47, 1 October 2015

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

Optic nerve glioma Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Optic nerve glioma from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

Chest X Ray

CT

MRI

Echocardiography or 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

Optic nerve glioma surgery On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Optic nerve glioma surgery

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Optic nerve glioma surgery

CDC on Optic nerve glioma surgery

Optic nerve glioma surgery in the news

Blogs on Optic nerve glioma surgery

Directions to Hospitals Treating Optic nerve glioma

Risk calculators and risk factors for Optic nerve glioma surgery

Overview

Surgery is not the first-line treatment option for patients with optic nerve glioma. Surgical excision is usually reserved for patients with either progressive proptosis, blindness, exophytic chiasm tumor causing mass effect, hydrocephalus, or with increased intracranial pressure.

Surgery

  • Usually surgery is not preferred for this type of tumor, but it can sometimes improve vision and/or relieve symptoms.
  • If the glioma causes an increase in intracranial pressure, excision may be required.
  • Where there is residual vision, excision is rarely utilized.
  • Surgical treatment for optic pathway gliomas usually involves either excision or biopsy of the tumor.
  • Surgery is the first choice when single nerve involvement is causing either progressive disfiguring proptosis, blindness, or an exophytic chiasm tumor is causing mass effect or hydrocephalus.
  • Biopsy is associated with some risk, and is not usually recommended for chiasmatic lesions involving visual pathway.
  • Diffuse infiltration of the chiasm is a contraindication to surgery.
  • Due to damage the risk of visual loss as well as damage to surrounding neurologic structures, surgical intervention for gliomas involving the optic chiasm is considered only for obtaining a biopsy specimen of the chiasm in certain cases or for relieving hydrocephalus.
  • NF-1 patients have increased risk of local recurrence after surgery than non-NF patients and tend to have less localized disease.

References

Template:WH Template:WS