Hirayama disease/cervical flexion-induced myelopathy progressing to spastic paraparesis: A report on three cases with literature review

被引:6
|
作者
Preethish-Kumar, Veeramani [1 ,2 ]
Polavarapu, Kiran [1 ,2 ]
Nashi, Saraswati [1 ]
Bhattacharya, Kajari [3 ]
Saini, Jitender [3 ]
Vengalil, Seena [1 ]
Pruthi, Nupur [4 ]
Bhat, Dhananjay I. [4 ]
Nalini, Atchayaram [1 ]
机构
[1] Natl Inst Mental Hlth & Neurosci, Dept Neurol, Bengaluru 560029, Karnataka, India
[2] Natl Inst Mental Hlth & Neurosci, Dept Clin Neurosci, Bengaluru 560029, Karnataka, India
[3] Natl Inst Mental Hlth & Neurosci, Dept Neuro Imaging & Intervent Radiol, Bengaluru 560029, Karnataka, India
[4] Natl Inst Mental Hlth & Neurosci, Dept Neurosurg, Bengaluru 560029, Karnataka, India
关键词
Cervical flexion-induced myelopathy; compressive myelopathy; Hirayama disease; long tract signs; spastic paraparesis; JUVENILE MUSCULAR-ATROPHY; UPPER EXTREMITY; SPINAL-CORD;
D O I
10.4103/0028-3886.236966
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Hirayama disease (HD)/cervical flexion-induced myelopathy (CFIM) is a lower motor neuron disease conventionally affecting a single upper extremity. We describe three men progressing after a long stable period to develop severe spastic paraparesis and bladder disturbances as a protracted implication of HD. The age at onset was 20, 24, and 15 years, while the age at presentation was 27, 41, and 57 years, respectively. The second phase of disease progression occurred after 4, 13, and 28 years of stationary period. All had CFIM with characteristic magnetic resonance imaging features as observed during progressive stages. The anterior dural shift extended variably from C4 to D4 levels with a median value of 5 mm and was maximum at C6 to C7 levels, pushing the cord anteriorly causing compression. This study emphasizes the need to recognize this unusual subgroup of HD and mandates long-term follow-up with timely intervention in arresting the progression/improving the deficits.
引用
收藏
页码:1094 / 1099
页数:6
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