CHANGES OF SONOGRAPHIC, MAGNETIC-RESONANCE TOMOGRAPHIC, ELECTROMYOGRAPHIC, AND HISTOPATHOLOGIC FINDINGS WITHIN A 2-MONTH PERIOD OF EXAMINATIONS AFTER EXPERIMENTAL MUSCLE DENERVATION
K. Kullmer et al., CHANGES OF SONOGRAPHIC, MAGNETIC-RESONANCE TOMOGRAPHIC, ELECTROMYOGRAPHIC, AND HISTOPATHOLOGIC FINDINGS WITHIN A 2-MONTH PERIOD OF EXAMINATIONS AFTER EXPERIMENTAL MUSCLE DENERVATION, Archives of orthopaedic and trauma surgery, 117(4-5), 1998, pp. 228-234
This study compares sonographical, histopathological, magnetic resonan
ce imaging (MRI), and electromyographical (EMG) findings following acu
te muscle denervation, We performed an experimental denervation of the
supraspinatus and infraspinatus muscles on 35 New Zealand white rabbi
ts by segment resection of the suprascapular nerve. The sonographical
appearance of the supraspinatus muscle was followed and documented at
short time intervals within a 2-month follow-up period, The sonographi
cal, histopathological, and MRI changes due to denervation suggest a r
egular pattern, Apart from the reduction of the muscle diameter, there
were considerable sonographical signs of denervation with an increase
of echointensity and inhomogenicity of echotexture that appeared on d
ay 14 after injury, and progressed continuously with time. MRI reveale
d a remarkable increase in signal intensity 3 weeks after denervation
and reproducible T2 times. Pathological spontaneous activity on EMG co
uld also be detected from day 14 after injury Conventional histopathol
ogical staining methods (H&E, NADH, ATPase, basic and acid phosphatase
) confirmed denervation and absence of reinnervation. The first nonspe
cific histopathological changes were seen 11 days after denervation in
the form of moderately atrophic fibers, Typical histopathological sig
ns of denervation appeared 3 weeks after nerve dissection. In summary,
EMC, ultrasound, MRI, and histopathology each showed first abnormalit
ies after about 2 weeks. In addition to EMG, sonography and MRI can do
cument the course of muscle atrophy and mesenchymal abnormalities in n
eurogenic muscle lesions.