Sporadic lower motor neuron disease with a snake eyes appearance on the cervical anterior horns by MRI

被引:7
作者
Sasaki, Shoichi [1 ]
机构
[1] Tokyo Womens Med Univ, Dept Neurol, Tokyo 1628666, Japan
关键词
Amyotrophic lateral sclerosis; Motor neuron disease; Lower motor neuron disease; Snake eyes appearance; MRI; AMYOTROPHIC-LATERAL-SCLEROSIS; JUVENILE MUSCULAR-ATROPHY; SPINAL-CORD; UPPER EXTREMITY; SPONDYLOTIC MYELOPATHY; ANTI-GM1; ANTIBODIES; SPECTRUM; NEUROPATHY; PATIENT;
D O I
10.1016/j.clineuro.2015.06.006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Lower motor neuron disease (LMND) is the term generally used to describe diseases in which only lower motor neuron signs are detected. A snake eyes appearance on magnetic resonance imaging (MRI) is associated with a wide spectrum of neurological conditions including LMND. The author reports on three unique LMND patients with upper limb muscle weakness and atrophy who show a snake eyes appearance by MRI. Patients and methods: The patients were aged 18, 40 and 52 years, respectively, at the onset of the disease and had a longstanding clinical course (more than 10 years for two patients and 8 years for one patient). They were followed up for more than 6 years. Results: Clinical manifestations were characterized by (1) longstanding slow progression or delayed spontaneous arrest of asymmetric lower motor neuron signs localized exclusively in the upper extremities with unilateral predominance and distal or proximal preponderance; (2) the absence of upper motor neuron signs, bulbar signs, sensory disturbances and respiratory involvement; (3) a snake eyes appearance on the anterior horns of the cervical cord over more than 3 vertebrae by axial T2-weighted MRI and a longitudinal linear-shaped T2-signal hyperintensity by sagittal MRI; (4) neurogenic change with fasciculation and denervation potentials (fibrillation and a positive sharp wave) confined to the affected muscles by needle electromyogram; and (5) normal cerebrospinal fluid and a normal creatine kinase level. These cases did not fall into any existing category of LMND, such as progressive muscular atrophy, flail arm syndrome or Hirayama disease. Conclusions: These patients should be classified as sporadic LMND with snake eyes on MRI with a relatively benign prognosis. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:122 / 131
页数:10
相关论文
共 39 条
[1]   The post-irradiation lower motor neuron syndrome - Neuronopathy or radiculopathy? [J].
Bowen, J ;
Gregory, R ;
Squier, M ;
Donaghy, M .
BRAIN, 1996, 119 :1429-1439
[2]   CENTRAL NERVOUS SYSTEM IN MOTOR NEURONE DISEASE [J].
BROWNELL, B ;
OPPENHEIMER, DR ;
HUGHES, JT .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1970, 33 (03) :338-+
[3]   ISOLATED GRANULOMATOUS-ANGIITIS OF THE SPINAL-CORD [J].
CACCAMO, DV ;
GARCIA, JH ;
HO, KL .
ANNALS OF NEUROLOGY, 1992, 32 (04) :580-582
[4]   MRI of the spinal cord in neuromyelitis optica and recurrent longitudinal extensive myelitis [J].
Cassinotto, C. ;
Deramond, H. ;
Olindo, S. ;
Aveillan, M. ;
Smadja, D. ;
Cabre, P. .
JOURNAL OF NEURORADIOLOGY, 2009, 36 (04) :199-205
[5]   Specific Pattern of Gadolinium Enhancement in Spondylotic Myelopathy [J].
Flanagan, Eoin P. ;
Krecke, Karl N. ;
Marsh, Richard W. ;
Giannini, Caterina ;
Keegan, B. Mark ;
Weinshenker, Brian G. .
ANNALS OF NEUROLOGY, 2014, 76 (01) :54-65
[6]   Motor neuron syndromes in cancer patients [J].
Forsyth, PA ;
Dalmau, J ;
Graus, F ;
Cwik, V ;
Rosenblum, MK ;
Posner, JB .
ANNALS OF NEUROLOGY, 1997, 41 (06) :722-730
[7]  
Fukutake T., 2006, SPINAL CORD, V19, P734
[8]   Owl's Eye in Spinal Magnetic Resonance Imaging [J].
Ghosh, Partha S. ;
Mitra, Sudeshna .
ARCHIVES OF NEUROLOGY, 2012, 69 (03) :407-408
[9]   MONOMELIC AMYOTROPHY [J].
GOURIEDEVI, M ;
SURESH, TG ;
SHANKAR, SK .
ARCHIVES OF NEUROLOGY, 1984, 41 (04) :388-394
[10]   Cervical dural sac and spinal cord in juvenile muscular atrophy of distal upper extremity [J].
Hirayama, K ;
Tokumaru, Y .
NEUROLOGY, 2000, 54 (10) :1922-1926