Peripheral neuropathy MRI: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
 
(2 intermediate revisions by 2 users not shown)
Line 1: Line 1:
__NOTOC__
__NOTOC__
{{Peripheral neuropathy}}
{{Peripheral neuropathy}}
Please help WikiDoc by adding more content here.  It's easy!  Click  [[Help:How_to_Edit_a_Page|here]]  to learn about editing.


{{CMG}} {{AE}} {{SME}}
{{CMG}}; {{AE}} {{MMJ}}
 
==Overview==
==Overview==
Magnetic resonance imaging (MRI) can examine muscle quality and size, detect any fatty replacement of muscle tissue, and determine whether a nerve fiber has sustained compression damage. The MRI equipment creates a strong magnetic field around the body. Radio waves are then passed through the body to trigger a resonance signal that can be detected at different angles within the body. A computer processes this resonance into either a three-dimensional picture or a two-dimensional "slice" of the scanned area.
MRI is not commonly used in diagnosis and evaluation of peripheral neuropathy but it may be helpful in the diagnosis of some kinds of peripheral neuropathy and other associated [[soft tissue]] damages. Normal nerves appear isointense to the surrounding tissue on T1- and T2-weighted (w) MRIs, but upon injury the nerves become hyperintense and thus visible on T2-w MRI. In certain instances, MRI may confer additional diagnostic advantages in peripheral neuropathy such as improved tissue characterization and imaging of deep or bone-encased structures. Interpretation of MRI of peripheral nerves requires availability of clinical differential diagnoses  and experience in performing studies. MRI may have some advantages in comparison to other non-invasive imaging methods of peripheral nerves imagings such as: Can be used to develop numerical [[nerve]] health standards for clinical applications, correlates with [[electrophysiology|electrophysiology,]] correlates with [[axon]] count and [[myelination]], has a high [[sensitivity]] and [[specificity]], determines stage of [[nerve]] [[injury]], MRI cannot examine long [[nerves]] in a single scan and cannot determine degree of [[nerve]] [[injury]].
 
==MRI==
 
*MRI is not commonly used in diagnosis and evaluation of peripheral neuropathy but it may be helpful in the diagnosis of some kinds of peripheral neuropathy and other associated [[soft tissue]] damages.<ref name="pmid1925277">{{cite journal| author=Noskin GA, Kalish SB| title=Pott's puffy tumor: a complication of intranasal cocaine abuse. | journal=Rev Infect Dis | year= 1991 | volume= 13 | issue= 4 | pages= 606-8 | pmid=1925277 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1925277  }} </ref><ref name="pmid25640096">{{cite journal| author=Low KT, Peh WC| title=Magnetic resonance imaging of diabetic foot complications. | journal=Singapore Med J | year= 2015 | volume= 56 | issue= 1 | pages= 23-33; quiz 34 | pmid=25640096 | doi= | pmc=4325563 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25640096  }} </ref>
*Normal nerves appear isointense to the surrounding tissue on T1- and T2-weighted (w) MRIs, but upon injury the nerves become hyperintense and thus visible on T2-w MRI. <ref name="pmid1925277">{{cite journal| author=Noskin GA, Kalish SB| title=Pott's puffy tumor: a complication of intranasal cocaine abuse. | journal=Rev Infect Dis | year= 1991 | volume= 13 | issue= 4 | pages= 606-8 | pmid=1925277 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1925277  }} </ref>
 
*In certain instances, MRI may confer additional diagnostic advantages in peripheral neuropathy such as improved tissue characterization and imaging of deep or bone-encased structures.<ref name="pmid23553474">{{cite journal| author=Zaidman CM, Seelig MJ, Baker JC, Mackinnon SE, Pestronk A| title=Detection of peripheral nerve pathology: comparison of ultrasound and MRI. | journal=Neurology | year= 2013 | volume= 80 | issue= 18 | pages= 1634-40 | pmid=23553474 | doi=10.1212/WNL.0b013e3182904f3f | pmc=4214100 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23553474  }} </ref>
*Interpretation of MRI of peripheral nerves requires availability of clinical differential diagnoses  and experience in performing studies.<ref name="pmid23553474">{{cite journal| author=Zaidman CM, Seelig MJ, Baker JC, Mackinnon SE, Pestronk A| title=Detection of peripheral nerve pathology: comparison of ultrasound and MRI. | journal=Neurology | year= 2013 | volume= 80 | issue= 18 | pages= 1634-40 | pmid=23553474 | doi=10.1212/WNL.0b013e3182904f3f | pmc=4214100 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23553474  }} </ref>
*MRI may have some advantages in comparison to other non-invasive imaging methods of peripheral nerves imagings such as:<ref name="pmid25766202">{{cite journal| author=Rangavajla G, Mokarram N, Masoodzadehgan N, Pai SB, Bellamkonda RV| title=Noninvasive imaging of peripheral nerves. | journal=Cells Tissues Organs | year= 2014 | volume= 200 | issue= 1 | pages= 69-77 | pmid=25766202 | doi=10.1159/000369451 | pmc=4494672 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25766202  }} </ref>
**Can be used to develop numerical [[nerve]] health standards for clinical applications
**Correlates with [[electrophysiology]]
**Correlates with [[axon]] count and [[myelination]]
**Has a high [[sensitivity]] and [[specificity]]
**Determines stage of [[nerve]] [[injury]]
 
*MRI cannot examine long [[nerves]] in a single scan and cannot determine degree of [[nerve]] [[injury]].<ref name="pmid25766202">{{cite journal| author=Rangavajla G, Mokarram N, Masoodzadehgan N, Pai SB, Bellamkonda RV| title=Noninvasive imaging of peripheral nerves. | journal=Cells Tissues Organs | year= 2014 | volume= 200 | issue= 1 | pages= 69-77 | pmid=25766202 | doi=10.1159/000369451 | pmc=4494672 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25766202  }} </ref>
 
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
[[Category:Mature chapter]]
 
[[Category:Disease]]
{{WH}}
[[Category:Psychiatry]]
{{WS}}
[[Category:Pediatrics]]
[[Category: (Name of the system)]]
[[Category:Gastroenterology]]
[[Category:primary care]]
[[Category:Geriatrics]]
[[Category:Needs content]]
{{WikiDoc Help Menu}}
{{WikiDoc Sources}}

Latest revision as of 15:22, 4 September 2018

Peripheral neuropathy Microchapters

Home

Patient Information

Overview

Classification

Pathophysiology

Causes

Differentiating peripheral neuropathy from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Peripheral neuropathy MRI On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Peripheral neuropathy MRI

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Peripheral neuropathy MRI

CDC on Peripheral neuropathy MRI

Peripheral neuropathy MRI in the news

Blogs on Peripheral neuropathy MRI

Directions to Hospitals Treating Psoriasis

Risk calculators and risk factors for Peripheral neuropathy MRI

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

Overview

MRI is not commonly used in diagnosis and evaluation of peripheral neuropathy but it may be helpful in the diagnosis of some kinds of peripheral neuropathy and other associated soft tissue damages. Normal nerves appear isointense to the surrounding tissue on T1- and T2-weighted (w) MRIs, but upon injury the nerves become hyperintense and thus visible on T2-w MRI. In certain instances, MRI may confer additional diagnostic advantages in peripheral neuropathy such as improved tissue characterization and imaging of deep or bone-encased structures. Interpretation of MRI of peripheral nerves requires availability of clinical differential diagnoses and experience in performing studies. MRI may have some advantages in comparison to other non-invasive imaging methods of peripheral nerves imagings such as: Can be used to develop numerical nerve health standards for clinical applications, correlates with electrophysiology, correlates with axon count and myelination, has a high sensitivity and specificity, determines stage of nerve injury, MRI cannot examine long nerves in a single scan and cannot determine degree of nerve injury.

MRI

  • MRI is not commonly used in diagnosis and evaluation of peripheral neuropathy but it may be helpful in the diagnosis of some kinds of peripheral neuropathy and other associated soft tissue damages.[1][2]
  • Normal nerves appear isointense to the surrounding tissue on T1- and T2-weighted (w) MRIs, but upon injury the nerves become hyperintense and thus visible on T2-w MRI. [1]
  • In certain instances, MRI may confer additional diagnostic advantages in peripheral neuropathy such as improved tissue characterization and imaging of deep or bone-encased structures.[3]
  • Interpretation of MRI of peripheral nerves requires availability of clinical differential diagnoses and experience in performing studies.[3]
  • MRI may have some advantages in comparison to other non-invasive imaging methods of peripheral nerves imagings such as:[4]

References

  1. 1.0 1.1 Noskin GA, Kalish SB (1991). "Pott's puffy tumor: a complication of intranasal cocaine abuse". Rev Infect Dis. 13 (4): 606–8. PMID 1925277.
  2. Low KT, Peh WC (2015). "Magnetic resonance imaging of diabetic foot complications". Singapore Med J. 56 (1): 23–33, quiz 34. PMC 4325563. PMID 25640096.
  3. 3.0 3.1 Zaidman CM, Seelig MJ, Baker JC, Mackinnon SE, Pestronk A (2013). "Detection of peripheral nerve pathology: comparison of ultrasound and MRI". Neurology. 80 (18): 1634–40. doi:10.1212/WNL.0b013e3182904f3f. PMC 4214100. PMID 23553474.
  4. 4.0 4.1 Rangavajla G, Mokarram N, Masoodzadehgan N, Pai SB, Bellamkonda RV (2014). "Noninvasive imaging of peripheral nerves". Cells Tissues Organs. 200 (1): 69–77. doi:10.1159/000369451. PMC 4494672. PMID 25766202.

Template:WH Template:WS