Neurofibroma: Difference between revisions

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==[[Neurofibroma overview|Overview]]==
==[[Neurofibroma historical perspective|Historical Perspective]]==
==[[Neurofibroma classification|Classification]]==
==[[Neurofibroma pathophysiology|Pathophysiology]]==
==[[Neurofibroma causes|Causes]]==
==[[Neurofibroma differential diagnosis|Differentiating Neurofibroma]]==
==[[Neurofibroma epidemiology and demographics|Epidemiology and Demographics]]==
==[[Neurofibroma risk factors|Risk Factors]]==
==[[Neurofibroma screening|Screening]]==
==[[Neurofibroma natural history, complications and prognosis|Natural History, Complications and Prognosis]]==
==Diagnosis==
[[Neurofibroma staging|Staging]] | [[Neurofibroma history and symptoms|History and Symptoms]] | [[Neurofibroma physical examination|Physical Examination]] | [[Neurofibroma laboratory findings|Laboratory Findings]]  | [[Neurofibroma x ray|X Ray]] | [[Neurofibroma CT|CT]] | [[Neurofibroma MRI|MRI]] [[Neurofibroma ultrasound|Ultrasound]] | [[Neurofibroma other imaging findings|Other Imaging Findings]] | [[Neurofibroma other diagnostic studies|Other Diagnostic Studies]] | [[Neurofibroma biopsy|Biopsy]]
==Treatment==
[[Neurofibroma medical therapy|Medical therapy]] | [[Neurofibroma surgery|Surgery]] | [[Neurofibroma primary prevention|Primary prevention]]  | [[Neurofibroma secondary prevention|Secondary prevention]] | [[Neurofibroma cost-effectiveness of therapy|Cost-Effectiveness of Therapy]] | [[Neurofibroma future or investigational therapies|Future or Investigational Therapies]]
==Case Studies==
[[Neurofibroma case study one|Case #1]]
==Overview==
==Overview==


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[[Category:Overview complete]]


{{Nervous tissue tumors}}
{{Nervous tissue tumors}}
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[[pl:Nerwiakowłókniak]]


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Revision as of 13:51, 12 November 2015

Neurofibroma Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Neurofibroma from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

Staging

History and Symptoms

Physical Examination

Laboratory Findings

X Ray

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

Neurofibroma On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Neurofibroma

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Neurofibroma

CDC on Neurofibroma

Neurofibroma in the news

Blogs on Neurofibroma

Directions to Hospitals Treating Neurofibroma

Risk calculators and risk factors for Neurofibroma

For patient information click here

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Kiran Singh, M.D. [2] Shanshan Cen, M.D. [3]

Synonyms and keywords:

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Neurofibroma

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Staging | History and Symptoms | Physical Examination | Laboratory Findings | X Ray | CT | MRI Ultrasound | Other Imaging Findings | Other Diagnostic Studies | Biopsy

Treatment

Medical therapy | Surgery | Primary prevention | Secondary prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies

Case Studies

Case #1


Overview

Neurofibroma is a type of nerve sheath tumor. In contrast to schwannomas - another type of tumor arising from the Schwann cells - neurofibromas incorporate all sorts of cells and structural elements in addition to the Schwann cells.[1]

Pathophysiology

Neurofibromas infiltrate the nerve and splay apart the individual nerve fibers. Although usually benign, Neurofibromas can sometimes degenerate into cancer.

Single neurofibromas often occur in middle and old age and grow at the margins of the peripheral nerves, displacing the nerve's main body.

The vestibulocochlear (acoustic) nerve is the most commonly affected, (see acoustic neuroma). Other cranial nerves and spinal nerves are less commonly involved.

Diagnosis

Physical Examination

Skin

Trunk

Treatment

Surgical resection is curative, although tumors are not easily removable if they surround important nerves such as the optic nerve. There is a risk of functional damage due to interference with the nerve. Debulking may be helpful.[3]

References

  1. Miller RT. Immunohistochemistry in the differential diagnosis of schwannoma and neurofibroma. Propath 2004 Oct. http://www.ihcworld.com/_newsletter/2004/2004-10_NF_vs_schwannoma_v1.pdf
  2. 2.0 2.1 "Dermatology Atlas".
  3. Babovic S, Bite U, Karnes PS, Babovic-Vuksanovic D (2003). "Liposuction: a less invasive surgical method of debulking plexiform neurofibromas". Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.] 29 (7): 785–7. PMID 12828709.

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