Neurogenic intermittent claudication caused by vasculitis in the cauda equina: an autopsy case report

被引:2
|
作者
Ando, Takashi [1 ,2 ]
Watanabe, Hazuki [3 ]
Riku, Yuichi [1 ,2 ]
Yoshida, Mari [2 ]
Goto, Yoji [3 ]
Ando, Ryota [4 ]
Fujino, Masahiko [4 ]
Ito, Masafumi [4 ]
Koike, Haruki [1 ]
Katsuno, Masahisa [1 ,5 ]
Iwasaki, Yasushi [2 ]
机构
[1] Nagoya Univ, Dept Neurol, Grad Sch Med, Showa Ku, 65 Tsurumai Cho, Nagoya, Aichi 4668550, Japan
[2] Aichi Med Univ, Inst Med Sci Aging, Dept Neuropathol, 1-1 Yazakokarimata, Nagakute, Aichi 4801195, Japan
[3] Japanese Red Cross Aichi Med Ctr Nagoya Daiichi H, Dept Neurol, Nakamura Ku, 3-35 Michishita Cho, Nagoya, Aichi 4538511, Japan
[4] Japanese Red Cross Aichi Med Ctr Nagoya Daiichi H, Dept Pathol, Nakamura Ku, 3-35 Michishita Cho, Nagoya, Aichi 4538511, Japan
[5] Nagoya Univ, Grad Sch Med, Dept Clin Res Educ, Showa Ku, 65 Tsurumai Cho, Nagoya, Aichi 4668550, Japan
关键词
Intermittent claudication; Cauda equina; Microscopic polyangiitis; Vasculitis; Stroke; Neuropathology; STENOSIS;
D O I
10.1007/s00586-022-07458-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose Intermittent claudication (IC) refers to leg pain that is induced by walking and relieved by rest. Neurogenic IC is usually associated with lumbar canal stenosis (LCS). We present rare findings from an autopsied patient who had neurogenic IC caused by vasculitis in the cauda equina. Methods We performed antemortem neurological and electrophysiological assessments, sural nerve biopsy, and post-mortem examination of the spinal cord and brain. Results A 61-year-old man noted sudden-onset leg pain that was not associated with any traumatic trigger. His leg pain consistently appeared when the patient walked and quickly faded on stopping. Spine surgery and cardiovascular departments both made a diagnosis of IC. However, magnetic resonance imaging (MRI) did not show LCS, and all ankle-brachial pressure indices were normal. He subsequently developed diffuse muscle weakness of the legs a month after disease onset. Myeloperoxidase antineutrophil cytoplasmic autoantibody was seropositive (140 IU/mL), and a sural nerve biopsy revealed axonal injury and angiitis. MRI showed multiple cerebral infarctions. He was diagnosed with microscopic polyangiitis (MPA) and underwent corticosteroid therapy. He died from complications two months after the onset. A post-mortem study revealed vasculitis in the subarachnoid space of the cauda equina, spinal cord, and brain parenchyma. The cauda equina showed a combined loss of small and large axonal fibres. The lumbar cord displayed central chromatolysis of the lower motor neurons. Conclusion MPA is a rare cause of neurogenic IC when the symptom is acute and multimodal. Small-vessel vasculitis affecting the cauda equina may underlie MPA-associated IC.
引用
收藏
页码:2602 / 2606
页数:5
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