Guillain-Barré syndrome physical examination: Difference between revisions

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===Appearance of the Patient===
===Appearance of the Patient===
*Patients with Guillain Barre syndrome might have abnormal gait.<ref name="pmid11320188" />  
*Patients with Guillain Barre syndrome might have abnormal gait.<ref name="pmid11320188">{{cite journal |vauthors=Mori M, Kuwabara S, Fukutake T, Yuki N, Hattori T |title=Clinical features and prognosis of Miller Fisher syndrome |journal=Neurology |volume=56 |issue=8 |pages=1104–6 |date=April 2001 |pmid=11320188 |doi= |url=}}</ref>  


===Vital Signs===
===Vital Signs===
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===Skin===
===Skin===
* Skin examination of patients with Guillain Barre syndrome is usually normal.
* Skin examination of patients with Guillain Barre syndrome is usually normal.
* We might see evidence of recent chicken pox disease.
* We might see evidence of recent chicken pox disease.<ref name="pmid3404161">{{cite journal |vauthors=Winer JB, Hughes RA, Anderson MJ, Jones DM, Kangro H, Watkins RP |title=A prospective study of acute idiopathic neuropathy. II. Antecedent events |journal=J. Neurol. Neurosurg. Psychiatry |volume=51 |issue=5 |pages=613–8 |date=May 1988 |pmid=3404161 |pmc=1033063 |doi= |url=}}</ref>
===HEENT===
===HEENT===
* Extra-ocular movements may be abnormal (ophthalmologist).<ref name="pmid11320188" />
* Extra-ocular movements may be abnormal (ophthalmologist).<ref name="pmid11320188" />
*Ophthalmoscopic exam may be abnormal with findings of papilledema.<ref name="pmid13493684" />
*Ophthalmoscopic exam may be abnormal with findings of papilledema.<ref name="pmid13493684">{{cite journal |vauthors=JOYNT RJ |title=Mechanism of production of papilledema in the Guillain-Barre syndrome |journal=Neurology |volume=8 |issue=1 |pages=8–12 |date=January 1958 |pmid=13493684 |doi= |url=}}</ref>
* Hearing acuity may be reduced.<ref name="pmid3399076" />
* Hearing acuity may be reduced.<ref name="pmid3399076">{{cite journal |vauthors=Nelson KR, Gilmore RL, Massey A |title=Acoustic nerve conduction abnormalities in Guillain-Barré syndrome |journal=Neurology |volume=38 |issue=8 |pages=1263–6 |date=August 1988 |pmid=3399076 |doi= |url=}}</ref>
* facial myokymia (Involuntary facial movement)<ref name="pmid6681885" />
* facial myokymia (Involuntary facial movement)<ref name="pmid6681885">{{cite journal |vauthors=Mateer JE, Gutmann L, McComas CF |title=Myokymia in Guillain-Barré syndrome |journal=Neurology |volume=33 |issue=3 |pages=374–6 |date=March 1983 |pmid=6681885 |doi= |url=}}</ref>
* vocal cord paralysis (Difficulty speaking)<ref name="pmid8441543" />
* vocal cord paralysis (Difficulty speaking)<ref name="pmid8441543">{{cite journal |vauthors=Panosian MS, Quatela VC |title=Guillain-Barré syndrome presenting as acute bilateral vocal cord paralysis |journal=Otolaryngol Head Neck Surg |volume=108 |issue=2 |pages=171–3 |date=February 1993 |pmid=8441543 |doi=10.1177/019459989310800211 |url=}}</ref>


===Neck===
===Neck===
* We might see some [[Lymphadenopathy]] because of prior infection with EBV or CMV.
* We might see some [[Lymphadenopathy]] because of prior infection with EBV or CMV.<ref name="pmid8784256">{{cite journal |vauthors=Irie S, Saito T, Nakamura K, Kanazawa N, Ogino M, Nukazawa T, Ito H, Tamai Y, Kowa H |title=Association of anti-GM2 antibodies in Guillain-Barré syndrome with acute cytomegalovirus infection |journal=J. Neuroimmunol. |volume=68 |issue=1-2 |pages=19–26 |date=August 1996 |pmid=8784256 |doi= |url=}}</ref><ref name="pmid3404161" />
* Using accessory muscle for breathing in severe cases.
* Using accessory muscle for breathing in severe cases.
===Lungs===
===Lungs===
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=== Common symptoms ===
Common symptoms of Guillain Barre syndrome include:
* Most of Guillain Barre syndrome cases can be diagnosed based on partially symmetrical ascending weakness and paralysis.  
* Most of Guillain Barre syndrome cases can be diagnosed based on partially symmetrical ascending weakness and paralysis.  
* Can cause sensory symptoms such as tingling and paresthesia.<ref name=":0">{{cite book | last = Mattle | first = Heinrich | title = Fundamentals of neurology : an illustrated guide | publisher = Thieme | location = Stuttgart New York | year = 2017 | isbn = 9783131364524 }}</ref>
* Can cause sensory symptoms such as tingling and paresthesia.<ref name=":0">{{cite book | last = Mattle | first = Heinrich | title = Fundamentals of neurology : an illustrated guide | publisher = Thieme | location = Stuttgart New York | year = 2017 | isbn = 9783131364524 }}</ref>
Line 90: Line 88:
*** Autonomic dysfunction in absent or mild.
*** Autonomic dysfunction in absent or mild.
*** AMSAN can causes severe type of GBS with slow recovery
*** AMSAN can causes severe type of GBS with slow recovery
** Miller Fisher syndrome<ref name="pmid11320188">{{cite journal |vauthors=Mori M, Kuwabara S, Fukutake T, Yuki N, Hattori T |title=Clinical features and prognosis of Miller Fisher syndrome |journal=Neurology |volume=56 |issue=8 |pages=1104–6 |date=April 2001 |pmid=11320188 |doi= |url=}}</ref>
*** This type of GBS causes ophthalmoplegia.
*** The reflexes are absence.
*** There is gait abnormalities (Ataxia).


=== Less Common Symptoms ===
*  
Less common symptoms of Guillain Barre syndrome include:
* Symptoms of papilledema such as
** Head ache
** Visual disturbance<ref name="pmid13493684">{{cite journal |vauthors=JOYNT RJ |title=Mechanism of production of papilledema in the Guillain-Barre syndrome |journal=Neurology |volume=8 |issue=1 |pages=8–12 |date=January 1958 |pmid=13493684 |doi= |url=}}</ref>
* Involuntary facial movement (facial myokymia)<ref name="pmid6681885">{{cite journal |vauthors=Mateer JE, Gutmann L, McComas CF |title=Myokymia in Guillain-Barré syndrome |journal=Neurology |volume=33 |issue=3 |pages=374–6 |date=March 1983 |pmid=6681885 |doi= |url=}}</ref>
* Hearing loss<ref name="pmid3399076">{{cite journal |vauthors=Nelson KR, Gilmore RL, Massey A |title=Acoustic nerve conduction abnormalities in Guillain-Barré syndrome |journal=Neurology |volume=38 |issue=8 |pages=1263–6 |date=August 1988 |pmid=3399076 |doi= |url=}}</ref>
* Difficulty speaking (vocal cord paralysis)<ref name="pmid8441543">{{cite journal |vauthors=Panosian MS, Quatela VC |title=Guillain-Barré syndrome presenting as acute bilateral vocal cord paralysis |journal=Otolaryngol Head Neck Surg |volume=108 |issue=2 |pages=171–3 |date=February 1993 |pmid=8441543 |doi=10.1177/019459989310800211 |url=}}</ref>
* Mental status changes<ref name="pmid16000335">{{cite journal |vauthors=Cochen V, Arnulf I, Demeret S, Neulat ML, Gourlet V, Drouot X, Moutereau S, Derenne JP, Similowski T, Willer JC, Pierrot-Deseiligny C, Bolgert F |title=Vivid dreams, hallucinations, psychosis and REM sleep in Guillain-Barré syndrome |journal=Brain |volume=128 |issue=Pt 11 |pages=2535–45 |date=November 2005 |pmid=16000335 |doi=10.1093/brain/awh585 |url=}}</ref>





Revision as of 18:43, 17 December 2018

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

Overview

It is included in the wider group of peripheral neuropathies. The physical examination findings usually indicates features due to autonomic dysfunction and demyelination of peripheral nerves. Fluctuation in vitals can be seen and may present as hyper or hypothermia, hypo or hypertension, brady or tachycardia. Progressive, symmetric, bilateral, flaccid, ascending paralysis progressing over weeks to days time is the common finding. Hypotonia, hyporeflexia, areflexia can be seen.Sensory system may be involved but generally it is mild. Ataxia and difficulty in walking may be seen despite great muscle strength due to involvement of proprioception and oculoparesis.

Physical Examination

Physical examination of patients with Guillain Barre syndrome is usually remarkable for:

Appearance of the Patient

  • Patients with Guillain Barre syndrome might have abnormal gait.[1]

Vital Signs

Skin

  • Skin examination of patients with Guillain Barre syndrome is usually normal.
  • We might see evidence of recent chicken pox disease.[3]

HEENT

  • Extra-ocular movements may be abnormal (ophthalmologist).[1]
  • Ophthalmoscopic exam may be abnormal with findings of papilledema.[4]
  • Hearing acuity may be reduced.[5]
  • facial myokymia (Involuntary facial movement)[6]
  • vocal cord paralysis (Difficulty speaking)[7]

Neck

  • We might see some Lymphadenopathy because of prior infection with EBV or CMV.[8][3]
  • Using accessory muscle for breathing in severe cases.

Lungs

  • Pulmonary examination of patients with Guillain barre syndrome is usually normal.

Heart

  • Cardiovascular examination of patients with Guillain Barre syndrome is usually normal.

Abdomen

  • Abdominal examination of patients with Guillain Barre syndrome is usually normal.

Back

  • Back examination of patients with Guillain Barre syndrome is usually normal.

Genitourinary

  • Evidences of urinary retention may be present.[2]

Neuromuscular

  • Neuromuscular examination of patients with [disease name] is usually normal.

OR

  • Patient is usually oriented to persons, place, and time
  • Altered mental status
  • Glasgow coma scale is ___ / 15
  • Clonus may be present
  • Hyperreflexia / hyporeflexia / areflexia
  • Positive (abnormal) Babinski / plantar reflex unilaterally/bilaterally
  • Muscle rigidity
  • Proximal/distal muscle weakness unilaterally/bilaterally
  • ____ (finding) suggestive of cranial nerve ___ (roman numerical) deficit (e.g. Dilated pupils suggestive of CN III deficit)
  • Unilateral/bilateral upper/lower extremity weakness
  • Unilateral/bilateral sensory loss in the upper/lower extremity
  • Positive straight leg raise test
  • Abnormal gait (describe gait: e.g. ataxic (cerebellar) gait / steppage gait / waddling gait / choeiform gait / Parkinsonian gait / sensory gait)
  • Positive/negative Trendelenburg sign
  • Unilateral/bilateral tremor (describe tremor, e.g. at rest, pill-rolling)
  • Normal finger-to-nose test / Dysmetria
  • Absent/present dysdiadochokinesia (palm tapping test)

Extremities

  • Extremities examination of patients with [disease name] is usually normal.

OR

  • Clubbing
  • Cyanosis
  • Pitting/non-pitting edema of the upper/lower extremities
  • Muscle atrophy
  • Fasciculations in the upper/lower extremity



  • Most of Guillain Barre syndrome cases can be diagnosed based on partially symmetrical ascending weakness and paralysis.
  • Can cause sensory symptoms such as tingling and paresthesia.[9]
  • Because of nerve inflammation, in the acute phase of GBS patients complain of pain.[10]
  • Some of the features may be specific to different subgroups of GBS.
    • Acute inflammatory demyelinating polyneuropathy:[2]
      • It affects lower extremities first and then involves upper extremities, trunk, neck and cranial nerves.
      • It can involve sensory neurons.
      • Deep sensation is the most affected sense.
      • It causes areflexia
      • In AIDP we may see autonomic involvement such as changes in heart rate and blood pressure and urinary retention.
    • Acute motor axonal neuropathy/Acute motor and sensory axonal neuropathy:[11][12]
      • Can causes hyperreflexia.
      • Autonomic dysfunction in absent or mild.
      • AMSAN can causes severe type of GBS with slow recovery


References

  1. 1.0 1.1 Mori M, Kuwabara S, Fukutake T, Yuki N, Hattori T (April 2001). "Clinical features and prognosis of Miller Fisher syndrome". Neurology. 56 (8): 1104–6. PMID 11320188.
  2. 2.0 2.1 2.2 Template:Victor, M., 2001. Diseases of spinal cord peripheral nerve and muscle. Principles of Neurology
  3. 3.0 3.1 Winer JB, Hughes RA, Anderson MJ, Jones DM, Kangro H, Watkins RP (May 1988). "A prospective study of acute idiopathic neuropathy. II. Antecedent events". J. Neurol. Neurosurg. Psychiatry. 51 (5): 613–8. PMC 1033063. PMID 3404161.
  4. JOYNT RJ (January 1958). "Mechanism of production of papilledema in the Guillain-Barre syndrome". Neurology. 8 (1): 8–12. PMID 13493684.
  5. Nelson KR, Gilmore RL, Massey A (August 1988). "Acoustic nerve conduction abnormalities in Guillain-Barré syndrome". Neurology. 38 (8): 1263–6. PMID 3399076.
  6. Mateer JE, Gutmann L, McComas CF (March 1983). "Myokymia in Guillain-Barré syndrome". Neurology. 33 (3): 374–6. PMID 6681885.
  7. Panosian MS, Quatela VC (February 1993). "Guillain-Barré syndrome presenting as acute bilateral vocal cord paralysis". Otolaryngol Head Neck Surg. 108 (2): 171–3. doi:10.1177/019459989310800211. PMID 8441543.
  8. Irie S, Saito T, Nakamura K, Kanazawa N, Ogino M, Nukazawa T, Ito H, Tamai Y, Kowa H (August 1996). "Association of anti-GM2 antibodies in Guillain-Barré syndrome with acute cytomegalovirus infection". J. Neuroimmunol. 68 (1–2): 19–26. PMID 8784256.
  9. Mattle, Heinrich (2017). Fundamentals of neurology : an illustrated guide. Stuttgart New York: Thieme. ISBN 9783131364524.
  10. Moulin DE, Hagen N, Feasby TE, Amireh R, Hahn A (February 1997). "Pain in Guillain-Barré syndrome". Neurology. 48 (2): 328–31. PMID 9040715.
  11. Kuwabara S, Ogawara K, Koga M, Mori M, Hattori T, Yuki N (August 1999). "Hyperreflexia in Guillain-Barré syndrome: relation with acute motor axonal neuropathy and anti-GM1 antibody". J. Neurol. Neurosurg. Psychiatry. 67 (2): 180–4. PMC 1736477.
  12. Kuwabara S, Nakata M, Sung JY, Mori M, Kato N, Hattori T, Koga M, Yuki N (July 2002). "Hyperreflexia in axonal Guillain-Barré syndrome subsequent to Campylobacter jejuni enteritis". J. Neurol. Sci. 199 (1–2): 89–92. PMID 12084449.

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