scholarly journals Central neuropathic pain in MS is due to distinct thoracic spinal cord lesions

2014 ◽  
Vol 1 (8) ◽  
pp. 554-561 ◽  
Author(s):  
Darin T. Okuda ◽  
Kara Melmed ◽  
Takashi Matsuwaki ◽  
Anders Blomqvist ◽  
Arthur D. Bud Craig
Pain ◽  
2008 ◽  
Vol 137 (2) ◽  
pp. 237-244 ◽  
Author(s):  
Sylvia M. Gustin ◽  
Paul J. Wrigley ◽  
Simon C. Gandevia ◽  
James W. Middleton ◽  
Luke A. Henderson ◽  
...  

2009 ◽  
Vol 25 (2) ◽  
pp. 167-169 ◽  
Author(s):  
Mi Geum Lee ◽  
Sang Sik Choi ◽  
Mi Kyoung Lee ◽  
Myoung Hoon Kong ◽  
Il Ok Lee ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Charidimos Tsagkas ◽  
Maria Janina Wendebourg ◽  
Matthias Mehling ◽  
Johannes Lorscheider ◽  
Philippe Lyrer ◽  
...  

Objective: Inflammatory polyradiculomyelitis belongs to a rare group of immune-mediated diseases affecting both the central and peripheral nervous system. We aimed to describe an unusual presentation of acute polyradiculomyelitis with marked spinal cord lesions restricted to the gray matter.Methods: Thorough examination of two case reports including clinical, MRI, serologic, electrophysiologic and CSF examinations as well as short-term follow-up.Results: We present two adult patients with acute polyradiculomyelitis and unusual spinal cord lesions restricted to the gray matter on MRI. The clinical presentation, serologic, electrophysiologic and CSF features of the two patients varied, whereas both patients demonstrated severe, asymmetrical, predominantly distal, motor deficits of the lower extremities as well as bladder and bowel dysfunction. Both patients only partially responded to anti-inflammatory treatment. Severe motor impairment and bladder dysfunction persisted even months after symptom onset.Conclusions: To our best of knowledge, these are the first reports of acute polyradiculomyelitis with distinct involvement of the lower thoracic spinal cord gray matter. Currently, it remains unclear whether gray matter lesions reflect a separate pathophysiologic mechanism or an exceedingly rare presentation of spinal cord involvement in acute polyradiculomyelitis.


Spinal Cord ◽  
2015 ◽  
Vol 53 (7) ◽  
pp. 520-525 ◽  
Author(s):  
L H Hua ◽  
S L Donlon ◽  
M J Sobhanian ◽  
S M Portner ◽  
D T Okuda

2011 ◽  
Vol 112 (2) ◽  
pp. 661-666 ◽  
Author(s):  
Keiko Sakamoto ◽  
Takeshi Nakamura ◽  
Yasunori Umemoto ◽  
Yumi Koike ◽  
Yusuke Sasaki ◽  
...  

2001 ◽  
Vol 45 (4) ◽  
pp. 353 ◽  
Author(s):  
Sung Chan Jin ◽  
Seoung Ro Lee ◽  
Dong Woo Park ◽  
Kyung Bin Joo

2018 ◽  
Vol 46 (05) ◽  
pp. 323-329 ◽  
Author(s):  
Nele Ondreka ◽  
Sara Malberg ◽  
Emma Laws ◽  
Martin Schmidt ◽  
Sabine Schulze

SummaryA 2-year-old male neutered mixed breed dog with a body weight of 30 kg was presented for evaluation of a soft subcutaneous mass on the dorsal midline at the level of the caudal thoracic spine. A further clinical sign was intermittent pain on palpation of the area of the subcutaneous mass. The owner also described a prolonged phase of urination with repeated interruption and re-initiation of voiding. The findings of the neurological examination were consistent with a lesion localization between the 3rd thoracic and 3rd lumbar spinal cord segments. Magnetic resonance imaging revealed a spina bifida with a lipomeningocele and diplomyelia (split cord malformation type I) at the level of thoracic vertebra 11 and 12 and secondary syringomyelia above the aforementioned defects in the caudal thoracic spinal cord. Surgical resection of the lipomeningocele via a hemilaminectomy was performed. After initial deterioration of the neurological status postsurgery with paraplegia and absent deep pain sensation the dog improved within 2 weeks to non-ambulatory paraparesis with voluntary urination. Six weeks postoperatively the dog was ambulatory, according to the owner. Two years after surgery the owner recorded that the dog showed a normal gait, a normal urination and no pain. Histopathological diagnosis of the biopsied material revealed a lipomeningocele which confirmed the radiological diagnosis.


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