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{{Acute brachial neuritis}}
{{Acute brachial neuritis}}
{{CMG}}
{{CMG}} {{AE}}
 
==Overview==
==Overview==
''Acute brachial neuritis'' (also known as Parsonage-Turner syndrome) is a rare syndrome of unknown etiology affecting mainly the [[lower motor neuron]]s of the [[brachial plexus]] and/or individual nerves or nerve branches. Acute brachial neuritis usually is characterized by the acute onset of excruciating unilateral [[shoulder pain]], followed by flaccid [[paralysis]] of shoulder and [[parascapular]] muscles after several days.
''Acute brachial neuritis'' (also known as Parsonage-Turner syndrome) is a rare syndrome of unknown etiology affecting mainly the [[lower motor neuron]]s of the [[brachial plexus]] and/or individual nerves or nerve branches. Acute brachial neuritis usually is characterized by the acute onset of excruciating unilateral [[shoulder pain]], followed by flaccid [[paralysis]] of shoulder and [[parascapular]] muscles after several days.
*[Disease name] was first discovered by [scientist name], a [nationality + occupation], in [year] during/following [event].
*In [year], [gene] mutations were first identified in the pathogenesis of [disease name].
*In [year], the first [discovery] was developed by [scientist] to treat/diagnose [disease name].
==Classification==
*[Disease name] may be classified according to [classification method] into [number] subtypes/groups:
:*[group1]
:*[group2]
:*[group3]
*Other variants of [disease name] include [disease subtype 1], [disease subtype 2], and [disease subtype 3].
==Pathophysiology==
*The pathogenesis of [disease name] is characterized by [feature1], [feature2], and [feature3].
*The [gene name] gene/Mutation in [gene name] has been associated with the development of [disease name], involving the [molecular pathway] pathway.
*On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
*On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].


==Causes==
==Causes==
Acute brachial neuritis is a form of [[peripheral neuropathy]]. It occurs when there is damage to the [[brachial plexus]], an area where a nerve bundle from the [[spinal cord]] splits into the individual arm [[nerves]].
Acute brachial neuritis is a form of [[peripheral neuropathy]]. It occurs when there is damage to the [[brachial plexus]], an area where a nerve bundle from the [[spinal cord]] splits into the individual arm [[nerves]].
==Differentiating [disease name] from other Diseases==
*[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as:
:*[Differential dx1]
:*[Differential dx2]
:*[Differential dx3]
==Epidemiology and Demographics==
==Epidemiology and Demographics==
In the USA each year, there are approximately 1 to 2 cases per 100,000 people. The reported incidence in the UK is 3 cases per 100,000 people.
In the USA each year, there are approximately 1 to 2 cases per 100,000 people. The reported incidence in the UK is 3 cases per 100,000 people.
==Natural History, Complications and Prognosis==
==Natural History, Complications and Prognosis==
The likely outcome depends on the cause. A good recovery is possible if the cause is identified and properly treatment. In some cases, there may be a partial or complete loss of movement or sensation. Nerve pain may be severe and may persist for a long time.
The likely outcome depends on the cause. A good recovery is possible if the cause is identified and properly treatment. In some cases, there may be a partial or complete loss of movement or sensation. Nerve pain may be severe and may persist for a long time.
==Risk Factors==
*Common risk factors in the development of [disease name] are [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
== Natural History, Complications and Prognosis==
*The majority of patients with [disease name] remain asymptomatic for [duration/years].
*Early clinical features include [manifestation 1], [manifestation 2], and [manifestation 3].
*If left untreated, [#%] of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
*Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
*Prognosis is generally [excellent/good/poor], and the [1/5/10­year mortality/survival rate] of patients with [disease name] is approximately [#%].
== Diagnosis ==
===Diagnostic Criteria===
*The diagnosis of [disease name] is made when at least [number] of the following [number] diagnostic criteria are met:
:*[criterion 1]
:*[criterion 2]
:*[criterion 3]
:*[criterion 4]
=== Symptoms ===
*[Disease name] is usually asymptomatic.
*Symptoms of [disease name] may include the following:
:*[symptom 1]
:*[symptom 2]
:*[symptom 3]
:*[symptom 4]
:*[symptom 5]
:*[symptom 6]
=== Physical Examination ===
*Patients with [disease name] usually appear [general appearance].
*Physical examination may be remarkable for:
:*[finding 1]
:*[finding 2]
:*[finding 3]
:*[finding 4]
:*[finding 5]
:*[finding 6]
=== Laboratory Findings ===
*There are no specific laboratory findings associated with [disease name].
*A  [positive/negative] [test name] is diagnostic of [disease name].
*An [elevated/reduced] concentration of [serum/blood/urinary/CSF/other] [lab test] is diagnostic of [disease name].
*Other laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].
===Imaging Findings===
*There are no [imaging study] findings associated with [disease name].
*[Imaging study 1] is the imaging modality of choice for [disease name].
*On [imaging study 1], [disease name] is characterized by [finding 1], [finding 2], and [finding 3].
*[Imaging study 2] may demonstrate [finding 1], [finding 2], and [finding 3].
=== Other Diagnostic Studies ===
*[Disease name] may also be diagnosed using [diagnostic study name].
*Findings on [diagnostic study name] include [finding 1], [finding 2], and [finding 3].
==Treatment==
==Treatment==
===Medical Therapy===
===Surgery===
===Surgery===
Some patients with [[brachial plexopathy]] may benefit from surgery if [[nerve compression]] is the cause of the symptoms.
Some patients with [[brachial plexopathy]] may benefit from surgery if [[nerve compression]] is the cause of the symptoms.
===Prevention===


==References==
==References==
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[[Category:Needs overview]]
[[Category:Disease]]
[[Category:Disease]]
[[Category:Emergency medicine]]
[[Category:Emergency medicine]]
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[[Category:Neurology]]
[[Category:Neurology]]
[[Category:Pediatrics]]
[[Category:Pediatrics]]
[[Category:Rheumatology]]


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Revision as of 12:43, 16 June 2016

Acute brachial neuritis Microchapters

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Overview

Historical Perspective

Classification

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Differentiating Acute brachial neuritis from other Diseases

Epidemiology and Demographics

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

Overview

Acute brachial neuritis (also known as Parsonage-Turner syndrome) is a rare syndrome of unknown etiology affecting mainly the lower motor neurons of the brachial plexus and/or individual nerves or nerve branches. Acute brachial neuritis usually is characterized by the acute onset of excruciating unilateral shoulder pain, followed by flaccid paralysis of shoulder and parascapular muscles after several days.

  • [Disease name] was first discovered by [scientist name], a [nationality + occupation], in [year] during/following [event].
  • In [year], [gene] mutations were first identified in the pathogenesis of [disease name].
  • In [year], the first [discovery] was developed by [scientist] to treat/diagnose [disease name].

Classification

  • [Disease name] may be classified according to [classification method] into [number] subtypes/groups:
  • [group1]
  • [group2]
  • [group3]
  • Other variants of [disease name] include [disease subtype 1], [disease subtype 2], and [disease subtype 3].

Pathophysiology

  • The pathogenesis of [disease name] is characterized by [feature1], [feature2], and [feature3].
  • The [gene name] gene/Mutation in [gene name] has been associated with the development of [disease name], involving the [molecular pathway] pathway.
  • On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
  • On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].

Causes

Acute brachial neuritis is a form of peripheral neuropathy. It occurs when there is damage to the brachial plexus, an area where a nerve bundle from the spinal cord splits into the individual arm nerves.

Differentiating [disease name] from other Diseases

  • [Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as:
  • [Differential dx1]
  • [Differential dx2]
  • [Differential dx3]

Epidemiology and Demographics

In the USA each year, there are approximately 1 to 2 cases per 100,000 people. The reported incidence in the UK is 3 cases per 100,000 people.

Natural History, Complications and Prognosis

The likely outcome depends on the cause. A good recovery is possible if the cause is identified and properly treatment. In some cases, there may be a partial or complete loss of movement or sensation. Nerve pain may be severe and may persist for a long time.

Risk Factors

  • Common risk factors in the development of [disease name] are [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].

Natural History, Complications and Prognosis

  • The majority of patients with [disease name] remain asymptomatic for [duration/years].
  • Early clinical features include [manifestation 1], [manifestation 2], and [manifestation 3].
  • If left untreated, [#%] of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
  • Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
  • Prognosis is generally [excellent/good/poor], and the [1/5/10­year mortality/survival rate] of patients with [disease name] is approximately [#%].

Diagnosis

Diagnostic Criteria

  • The diagnosis of [disease name] is made when at least [number] of the following [number] diagnostic criteria are met:
  • [criterion 1]
  • [criterion 2]
  • [criterion 3]
  • [criterion 4]

Symptoms

  • [Disease name] is usually asymptomatic.
  • Symptoms of [disease name] may include the following:
  • [symptom 1]
  • [symptom 2]
  • [symptom 3]
  • [symptom 4]
  • [symptom 5]
  • [symptom 6]

Physical Examination

  • Patients with [disease name] usually appear [general appearance].
  • Physical examination may be remarkable for:
  • [finding 1]
  • [finding 2]
  • [finding 3]
  • [finding 4]
  • [finding 5]
  • [finding 6]

Laboratory Findings

  • There are no specific laboratory findings associated with [disease name].
  • A [positive/negative] [test name] is diagnostic of [disease name].
  • An [elevated/reduced] concentration of [serum/blood/urinary/CSF/other] [lab test] is diagnostic of [disease name].
  • Other laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].

Imaging Findings

  • There are no [imaging study] findings associated with [disease name].
  • [Imaging study 1] is the imaging modality of choice for [disease name].
  • On [imaging study 1], [disease name] is characterized by [finding 1], [finding 2], and [finding 3].
  • [Imaging study 2] may demonstrate [finding 1], [finding 2], and [finding 3].

Other Diagnostic Studies

  • [Disease name] may also be diagnosed using [diagnostic study name].
  • Findings on [diagnostic study name] include [finding 1], [finding 2], and [finding 3].

Treatment

Medical Therapy

Surgery

Some patients with brachial plexopathy may benefit from surgery if nerve compression is the cause of the symptoms.

Prevention

References

Template:WH Template:WS