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Bilaterally symmetric form of
hirayama disese
• Sunil Pradhan et al
• Institute of human behavior and allied
sciences, New delhi.
• Neurology,vol.72,number 24,june16,2009.
background
• Hirayama disease (benign juvenile brachial spinal muscular
atrophy, benign juvenile muscular atrophy of distal upper
extremity, monomelic amyotrophy).
• Pure motor focal amyotrophy in distribution of c7,8,T1 spinal
segments
• Sporadic, Men, second and early third decade.
• Muscular weakness and wasting of hand and forearm
• Oblique amyotrophy.
• Insidious onset, steadily progressive for 1-3 yrs..stable
stage.
• Dynamic cord compression during neck flexion.
• Juvenile asymmetric segmental spinal muscular
atrophy(JASSMA)
• Describe bilaterally symmetric form of hirayama disease.
Materials and methods
• 106 (m-103,f-3)
• 14-32 yrs
• Two academic centers
• 1992-2008
• Patients registry
• 11 patients with symmetic form
• Clinical, edx, mri evaluation normal and neck flexion.
criteria
• Onset in teen and early 20s.
• Symmetric /asymmetric muscle atrophy in c7,c8,t1
myotome.
• No sensory symptoms/signs
• Relative sparing of brachioradialis
• Tremulousness of fingers in outstretched hands
• Cold paresis
• Unilaterality ….replaced by MRI findigs
MRI criteria
• Flattening of spinal cord against c5-6 vertebral bodies
• Forward movement of posterior cervical duramater,
• reduction in size of posterior cervical subarachnoid
space.
• Contrast enhancing crescent shaped posterior cervical
epidural pace.
EMG
• 1stdorsalinterossei,APB,EDC,brachioradialis,biceps,vast
us lateralis,tibialis anterior.
• Denervation potentials( positive sharp waves and
otentials)during rest state were compared in same
muscle in two sides.
• Reinervation potentials (large,wide polyphasic
potentials)studied in mild contraction in each muscle(3
x3)
• 10 sweeps of 100 msec duration-frozen –percent of
polyphasic potentials to number of MUP and compared.
NCS
• CMAP of median,ulnar,radial nerve were used to
document symmetry of disease.
• < 20% difference in CMAP of APB,ADM,EDC taken as
symmetrical.
• SNC to rule out axonal forms of polyneuropathy
• All findings were compared with existing knowledge of
the disease
results
• 11/106 symmetrical
• All male
• Age 18-24(20.27)
• Started at mean 17.8 yrs progresed for 1-3 yrs (9),3-4
yrs (2)
• 9 immunised for polio, none had h/o polio.
• 6 had onset in winter months
• None had preceding febrile illness
• All had weakness and wasting in c5,6 t1 myotomes
• 6 had partial brachioradialis wasting s/o c6 myotome
• Unilateral onset in 9 patients (R 6, L 3),bilateral in two.
• Autonomic dysfunction in all, (excessive sweating in
7,cold hands in 8,hair loss in 5)
• All had fasciculation at rest ,mini polymyoclonus in
outstretched hands.
• 7 had brisk DTR in lower limbs
mri
• Neutral position-Symmetric cord atrophy in 9, T2 hyper
intensity in anterior lateral aspect of lower cervical spinal
cord in 7.
• Neck flexion-band like cord flattening in all (symmetric in
7,asymmetric in 4)crescent shaped enhancing epidural
in all.
EDX
• All had N SNAPs
• All had n emg in lower limbs
• All clinicallly symmetric form had < 20% difference in
CMAPs.
• Quantitative asessment of percentage of acute
denervation and chronic renervation potentials showed
nearly symmetric involvement between right and left
discussion
• In this series of 106 patients nearly 10% showed
symmetric involvement of both upperlimbs.
• VS a form of ALS ‘brachial amyotrophic diplegia’ ‘flail
arm syndrome’ ‘man in barrel syndrome’-older age,
predominant c5-6 involvement, overt fasciculations,
gradual appearance of UMN or bulbar signs,avg survival
of 5 yrs,no dynamic MRI changes with neck flexion.
• Vs postpolio atrophy-no h/o polio,symmetrical and MRI.
• Short length of cervical dural canal that cannot
compensate for flexion related increased length of
vertebral canal. dural canal becomes tight during neck
flexion-anterior displacement of posterior dural wall and
spinal cord, spinal cord gets flattened against c5-6
vertebral body,cresent shaped posterior epidural space
with prominent venous plexus.
• Neck flexion related anatomic changes cause
mechanical and hemodynamic stress on anterior horn
cells in c7,8,T1
• Severe form of hirayama disease
• Thank you
Hirayama jc
Hirayama jc
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Hirayama jc
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Hirayama jc

  • 1. Bilaterally symmetric form of hirayama disese • Sunil Pradhan et al • Institute of human behavior and allied sciences, New delhi. • Neurology,vol.72,number 24,june16,2009.
  • 2. background • Hirayama disease (benign juvenile brachial spinal muscular atrophy, benign juvenile muscular atrophy of distal upper extremity, monomelic amyotrophy). • Pure motor focal amyotrophy in distribution of c7,8,T1 spinal segments • Sporadic, Men, second and early third decade. • Muscular weakness and wasting of hand and forearm • Oblique amyotrophy. • Insidious onset, steadily progressive for 1-3 yrs..stable stage. • Dynamic cord compression during neck flexion. • Juvenile asymmetric segmental spinal muscular atrophy(JASSMA) • Describe bilaterally symmetric form of hirayama disease.
  • 3. Materials and methods • 106 (m-103,f-3) • 14-32 yrs • Two academic centers • 1992-2008 • Patients registry • 11 patients with symmetic form • Clinical, edx, mri evaluation normal and neck flexion.
  • 4. criteria • Onset in teen and early 20s. • Symmetric /asymmetric muscle atrophy in c7,c8,t1 myotome. • No sensory symptoms/signs • Relative sparing of brachioradialis • Tremulousness of fingers in outstretched hands • Cold paresis • Unilaterality ….replaced by MRI findigs
  • 5. MRI criteria • Flattening of spinal cord against c5-6 vertebral bodies • Forward movement of posterior cervical duramater, • reduction in size of posterior cervical subarachnoid space. • Contrast enhancing crescent shaped posterior cervical epidural pace.
  • 6. EMG • 1stdorsalinterossei,APB,EDC,brachioradialis,biceps,vast us lateralis,tibialis anterior. • Denervation potentials( positive sharp waves and otentials)during rest state were compared in same muscle in two sides. • Reinervation potentials (large,wide polyphasic potentials)studied in mild contraction in each muscle(3 x3) • 10 sweeps of 100 msec duration-frozen –percent of polyphasic potentials to number of MUP and compared.
  • 7. NCS • CMAP of median,ulnar,radial nerve were used to document symmetry of disease. • < 20% difference in CMAP of APB,ADM,EDC taken as symmetrical. • SNC to rule out axonal forms of polyneuropathy • All findings were compared with existing knowledge of the disease
  • 8. results • 11/106 symmetrical • All male • Age 18-24(20.27) • Started at mean 17.8 yrs progresed for 1-3 yrs (9),3-4 yrs (2) • 9 immunised for polio, none had h/o polio. • 6 had onset in winter months • None had preceding febrile illness • All had weakness and wasting in c5,6 t1 myotomes • 6 had partial brachioradialis wasting s/o c6 myotome
  • 9. • Unilateral onset in 9 patients (R 6, L 3),bilateral in two. • Autonomic dysfunction in all, (excessive sweating in 7,cold hands in 8,hair loss in 5) • All had fasciculation at rest ,mini polymyoclonus in outstretched hands. • 7 had brisk DTR in lower limbs
  • 10. mri • Neutral position-Symmetric cord atrophy in 9, T2 hyper intensity in anterior lateral aspect of lower cervical spinal cord in 7. • Neck flexion-band like cord flattening in all (symmetric in 7,asymmetric in 4)crescent shaped enhancing epidural in all.
  • 11. EDX • All had N SNAPs • All had n emg in lower limbs • All clinicallly symmetric form had < 20% difference in CMAPs. • Quantitative asessment of percentage of acute denervation and chronic renervation potentials showed nearly symmetric involvement between right and left
  • 12. discussion • In this series of 106 patients nearly 10% showed symmetric involvement of both upperlimbs. • VS a form of ALS ‘brachial amyotrophic diplegia’ ‘flail arm syndrome’ ‘man in barrel syndrome’-older age, predominant c5-6 involvement, overt fasciculations, gradual appearance of UMN or bulbar signs,avg survival of 5 yrs,no dynamic MRI changes with neck flexion. • Vs postpolio atrophy-no h/o polio,symmetrical and MRI.
  • 13. • Short length of cervical dural canal that cannot compensate for flexion related increased length of vertebral canal. dural canal becomes tight during neck flexion-anterior displacement of posterior dural wall and spinal cord, spinal cord gets flattened against c5-6 vertebral body,cresent shaped posterior epidural space with prominent venous plexus. • Neck flexion related anatomic changes cause mechanical and hemodynamic stress on anterior horn cells in c7,8,T1 • Severe form of hirayama disease
  • 14.