Difference between revisions of "Neuromuscular pathology"

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| groups <br>("group atrophy")
| groups <br>("group atrophy")
| singular
| singular
|
|  
| [http://neuropathology.neoucom.edu/chapter9/images9/13-7.jpg group atrophy]<ref>URL: [http://neuropathology.neoucom.edu/chapter9/chapter9fALS.html http://neuropathology.neoucom.edu/chapter9/chapter9fALS.html]. Accessed on: 25 October 2010.</ref>
| [http://neuropathology.neoucom.edu/chapter9/images9/13-7.jpg group atrophy]<ref>URL: [http://neuropathology.neoucom.edu/chapter9/chapter9fALS.html http://neuropathology.neoucom.edu/chapter9/chapter9fALS.html]. Accessed on: 25 October 2010.</ref>
|-
|-
Line 39: Line 39:
| No
| No
| +/-Scattered
| +/-Scattered
| "hypercontracted fibres"
| "hypercontracted<br>fibres"
| [http://commons.wikimedia.org/wiki/File:Duchenne-muscular-dystrophy.jpg DMD (WC)]
| [http://commons.wikimedia.org/wiki/File:Duchenne-muscular-dystrophy.jpg DMD (WC)]
|-
| Fibre type<br>grouping
| yes (d/t chronic <br>denervation + <br>reinnervation)<ref>URL: [http://neuromuscular.wustl.edu/lab/mbiopsy.htm#fibertype http://neuromuscular.wustl.edu/lab/mbiopsy.htm#fibertype]. Accessed on: 26 October 2010.</ref>
| yes (???)
| based on ATPase, NADH-TR stains
| [http://missinglink.ucsf.edu/lm/ids_104_musclenerve_path/student_musclenerve/subpages/ng.atp.9.4.1.html]<ref>URL: [http://missinglink.ucsf.edu/lm/ids_104_musclenerve_path/student_musclenerve/musclepath.html http://missinglink.ucsf.edu/lm/ids_104_musclenerve_path/student_musclenerve/musclepath.html]. Accessed on: 26 October 2010.</ref>
|}
|}


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==Stains for muscle biopsies==
==Stains for muscle biopsies==
Common/standard:
===Standard===
*H&E stain.
{| class="wikitable"
*Gomori trichrome - Good for nemaline rods, mitochondrial pathology (red).
| '''Stain'''
*PAS.
| '''Comment'''
*Congo red - find [[amyloid]]; seen in inclusion body myositis.
| '''Image'''
*Oil Red O - type 1 more lipid.
|-
*ATPase - should have checkerboard pattern in normal.
| H&E stain
*NADH-TR - should have checkerboard pattern in normal.
| routine
 
| [http://www.rvc.ac.uk/Research/Labs/NeuroLab/images/HE.jpg]<ref>URL: [http://www.rvc.ac.uk/Research/Labs/NeuroLab/MuscleBiopsy.cfm http://www.rvc.ac.uk/Research/Labs/NeuroLab/MuscleBiopsy.cfm]. Accessed on: 26 October 2010.</ref>
|-
| Gomori trichrome
| good for nemaline rods, <br>mitochondrial pathology (appear red)
| [http://commons.wikimedia.org/wiki/File:Modified_Gomori_trichrome_stain_showing_several_ragged_red_fibers_.jpg]
|-
| PAS
| glycogen storage disorders
| [http://neuromuscular.wustl.edu/pics/biopsy/dm/dermatopas.jpg]<ref>URL: [http://neuromuscular.wustl.edu/pathol/dermmyo.htm http://neuromuscular.wustl.edu/pathol/dermmyo.htm]. Accessed on: 26 October 2010.</ref>
|-
| Congo red  
| find [[amyloid]]; seen in<br>inclusion body myositis
| [http://neuromuscular.wustl.edu/pics/biopsy/lgd/ibmpaget/hppagetibmvaccr2.jpg]<ref>URL: [http://neuromuscular.wustl.edu/pathol/ibmpaget.htm http://neuromuscular.wustl.edu/pathol/ibmpaget.htm]. Accessed on: 26 October 2010.</ref>
|-
| Oil red O  
| lipid more in<br> type 1 fibres
|
|-
| ATPase pH4.2<br>ATPase pH9.4
| should have "checkerboard <br>pattern" in normal; see table below
| [http://neuromuscular.wustl.edu/pics/biopsy/dm/dermatopfatp94.jpg]<ref>URL: [http://neuromuscular.wustl.edu/pathol/dermmyo.htm http://neuromuscular.wustl.edu/pathol/dermmyo.htm]. Accessed on: 26 October 2010.</ref>
|-
| NADH-TR  
| should have "checkerboard <br>pattern" in normal
|
|}
Special - mitochondrial pathology.:
Special - mitochondrial pathology.:
*SDH.
*SDH (Succinate dehydrogenase).
*COX.
*COX.
*COX-SDH.
*COX-SDH.
Line 138: Line 169:


Dunno:
Dunno:
*Toluidine blue.
*Toluidine blue - myopathies.  
**Image: [http://neuromuscular.wustl.edu/pics/biopsy/rods/rodhptb2.jpg Nemaline rods (wustl.edu)].<ref>URL: [http://neuromuscular.wustl.edu/pathol/rod.htm http://neuromuscular.wustl.edu/pathol/rod.htm]. Accessed on: 26 October 2010.</ref>


IHC:
IHC:
Line 294: Line 326:
==External links==
==External links==
*[http://moon.ouhsc.edu/kfung/jty1/NeuroHelp/ZNEWWU10.htm How to work up a muscle biopsy (ouhsc.edu)].
*[http://moon.ouhsc.edu/kfung/jty1/NeuroHelp/ZNEWWU10.htm How to work up a muscle biopsy (ouhsc.edu)].
*[http://neuromuscular.wustl.edu/lab/mbiopsy.htm Muscle biopsies (wustl.edu)].


[[Category:Neuropathology]]
[[Category:Neuropathology]]

Revision as of 03:34, 27 October 2010

Neuromuscular pathology is the study of muscle and neurologic disease associated with muscle dysfunction. It is a part of neuropathology.

Muscle pathology is dealt together with neurologic disease as, at the presentation, they are not infrequently impossible to definitely distinguish.

Work-up

  1. Clinical history, including family history.
  2. Laboratory studies, e.g. CK.
  3. Nerve conduction and electromyography studies.
  4. Muscle biopsy.

Patterns

Overview

 
 
 
 
 
 
 
 
Neuromuscular
pathology
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Neurogenic
 
 
Myogenic
 
 
Other/Mixed
Neurogenic Myogenic Notes Image
Shape of fibres angulated round round fibres[1]
Small fibres groups
("group atrophy") 		singular group atrophy[2]
Large fibres
 No +/-Scattered "hypercontracted
fibres" 		DMD (WC)
Fibre type
grouping 		yes (d/t chronic
denervation +
reinnervation)[3] 		yes (???) based on ATPase, NADH-TR stains [1][4]

List

Neurogenic:

  • Angulated myocytes.
  • Groups of small fibres.
  • Apparent increase of nuclei.

Myogenic:

  • Round myocytes.
  • +/-Intense (darker) cytoplasm.
  • +/-Fibrosis (between fibres).
  • +/-Necrosis.

Detail

  1. Segmental demyelination - nerve/CNS abnormality.
  2. Axonal degeneration - nerve/CNS abnormality.
  3. Reinnervation - nerve injury.
  4. Myopathy - something is wrong with the muscle fibres.

Muscle structure/histology

Macro to micro

Organization:[5]

  • Muscle - surrounded by epimysium.
    • Fascicle - surrounded by perimysium.
      • Muscle fibre - muscle cell.
        • Myofibrils - contractile elements within the muscle cell.

Fibre types

 
 
 
Types
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Type 1
slow twitch
 
 
 
Type 2
fast twitch

List

Type 1 - AKA slow twitch:

  • Predominantly oxidative metabolism, i.e. have lots of mitochondria.

Type 2 - AKA fast twitch:

  • Predominantly glycolytic metabolism.

Mnemonic Slow red fat ox: Slow twitch fibres are (grossly) more red (due to mitochondria), lipid rich (fat) and primarily have oxidative metabolism.

Abnormal findings

  • Ragged red fibres = mitochondrial pathology.
  • Rimmed vacuoles = inclusion body myositis.
  • PAS +++ = glycogen storage disease.
  • Regenerative fibres = large nuclei, basophilic cytoplasm (incr. protein synthesis, incr. RNA).

Others:

  • Target fibre - "hole in middle of myofibres" = neurogenic. (???)
  • Cores - central pale area along length of fibres = myopathic. (???)

Approach

General:

  1. Size variation - in groups (neurogenic) vs. singular (myogenic).
  2. Shape - angulated (neurogenic) vs. round (myogenic).
  3. Position of nuclei.
  4. Necrosis - suggests myogenic.
  5. Fibrosis - suggests myogenic.
  6. Inflammation.

Other:

  1. Obvious abnormality vs. minimal change.
  2. Diffuse vs. focal change.

Processing of muscle biopsies

  1. Formulin.
  2. Frozen section.
  3. Frozen for biochemistry.
  4. Fragment for electronmicroscopy (glutaraldehyde fixative).

Stains for muscle biopsies

Standard

Stain Comment Image
H&E stain routine [2][6]
Gomori trichrome good for nemaline rods,
mitochondrial pathology (appear red) 		[3]
PAS glycogen storage disorders [4][7]
Congo red find amyloid; seen in
inclusion body myositis 		[5][8]
Oil red O lipid more in
type 1 fibres
ATPase pH4.2
ATPase pH9.4 		should have "checkerboard
pattern" in normal; see table below 		[6][9]
NADH-TR should have "checkerboard
pattern" in normal

Special - mitochondrial pathology.:

  • SDH (Succinate dehydrogenase).
  • COX.
  • COX-SDH.

Enzymatic/genetic stuff:

  • Phosphorylase.
  • Adenylate deaminase.
  • Acid phosphatase.
  • Alkaline phosphatase.

Dunno:

IHC:

  • Dystrophy panel.
  • Lymphocytic markers (CD45, CD3, CD4, CD8, CD20).
  • MAC - inclusion body myositis.
  • APP - inclusion body myositis.
  • Ubquitin - inclusion body myositis.

ATPase stain pattern/fibre type

Type 1
slow twitch 		Type 2
fast twitch
pH 4.2 dark light
pH 9.4 light dark

Inflammatory myopathy

DDx:

  1. Polymyositis.
  2. Inclusion body myositis.
  3. Dermatomyositis.

DDx

Neurogenic:

  • Amyotrophic lateral sclerosis.
  • Spinal muscular atrophy.
  • Trauma.
  • Vascular disease.
  • Infective process.
  • ?Motor neuron disease.

Myopathic:

  • Inflammatory:
    1. Polymyositis.
    2. Inclusion body myositis.
    3. Dermatomyositis.
  • Duchenne muscular dystrophy.
  • Becker muscular dystrophy.
  • Limb-girdle muscular dystrophy.
  • Myotonic dystrophy.
  • Metabolic - glycogen storage disease.

Other:

  • Myasthenia gravis.
  • Mitochondrial myopathy.
  • Congenital fibre type disproportion.
  • Periodic paralysis.

Amyotrophic lateral sclerosis

General

  • Abbreviated ALS.
  • Affects - corticospinal tract - gliosis.

Microscopic

Features:

  • Neurogenic pattern:
    • Group atrophy.
    • +/-Target fibre.

Dermatomyositis

General

  • Complement mediated disease... membrane attach complex.
  • Usually middle age. (???)
  • Associated skin rash is common. (???)

Microscopic

Features:

  • Perifascicular inflammation with perifascicular atrophy - key feature.

Inclusion body myositis

General

  • Usually elderly.

Microscopic

Features:

  • Inflammation.
  • Vacuolated fibres (with proteineous aggregates) - key feature.

DDx: polymyositis.

IHC: APP +ve, ubiquitin +ve, tau +ve.

Polymyositis

General

  • Tx: steroids.

Microscopic

Features:

  • Inflammation.

DDx: Inclusion body myositis.

Muscular dystrophy

General

  • DDx: large.

Microscopic

Features:

  • Endomysial fibrosis.
  • Hypercontracted fibres (large muscle fibres).

Myotonic dystrophy

Microscopic

Features:

  • Internal nuclei/central nuclei.

Nemaline myopathy

General

  • A type of congenital myopathy.
  • Paediatric thingy.


Mitochondrial disorders

General

  • Onset childhood to adulthood.
  • Heteroplasmy - variable distribution of badness within affected individuals.
    • Leads to "threshold effect".

Microscopic

  • Trichrome most useful - find the ragged red fibres - usu. at the cell periphery.
  • COX-SDH - non-staining.

EM

Features:

  • Crystalloid inclusions[11]

Type 2 fibre atrophy

DDx:

  • Disuse.
  • Space travel.
  • Steroids.
  • Others.

Nerve stuff

General

  • Biopsy: sural nerve.
  • Myelin stain: blue = myelin.
  • Gomori trichrome: axon = green, myelin = red.

See also

References

  1. ↑ URL: http://nmdinfo.org/lectures/info.php?id=8. Accessed on: 25 October 2010.
  2. ↑ URL: http://neuropathology.neoucom.edu/chapter9/chapter9fALS.html. Accessed on: 25 October 2010.
  3. ↑ URL: http://neuromuscular.wustl.edu/lab/mbiopsy.htm#fibertype. Accessed on: 26 October 2010.
  4. ↑ URL: http://missinglink.ucsf.edu/lm/ids_104_musclenerve_path/student_musclenerve/musclepath.html. Accessed on: 26 October 2010.
  5. ↑ URL: http://commons.wikimedia.org/wiki/File:Skeletal_muscle.jpg. Accessed on: 25 October 2010.
  6. ↑ URL: http://www.rvc.ac.uk/Research/Labs/NeuroLab/MuscleBiopsy.cfm. Accessed on: 26 October 2010.
  7. ↑ URL: http://neuromuscular.wustl.edu/pathol/dermmyo.htm. Accessed on: 26 October 2010.
  8. ↑ URL: http://neuromuscular.wustl.edu/pathol/ibmpaget.htm. Accessed on: 26 October 2010.
  9. ↑ URL: http://neuromuscular.wustl.edu/pathol/dermmyo.htm. Accessed on: 26 October 2010.
  10. ↑ URL: http://neuromuscular.wustl.edu/pathol/rod.htm. Accessed on: 26 October 2010.
  11. ↑ URL: http://moon.ouhsc.edu/kfung/jty1/neurotest/Q09-Ans.htm. Accessed on: 26 October 2010.

External links

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