Coexistence of amyotrophic lateral sclerosis with neuro‐Behçet's disease presenting as a longitudinally extensive spinal cord lesion: clinicopathologic features of an autopsied patient. Issue 2 (30th September 2013)
- Record Type:
- Journal Article
- Title:
- Coexistence of amyotrophic lateral sclerosis with neuro‐Behçet's disease presenting as a longitudinally extensive spinal cord lesion: clinicopathologic features of an autopsied patient. Issue 2 (30th September 2013)
- Main Title:
- Coexistence of amyotrophic lateral sclerosis with neuro‐Behçet's disease presenting as a longitudinally extensive spinal cord lesion: clinicopathologic features of an autopsied patient
- Authors:
- Sato, Tomoe
Ouchi, Haruka
Shimbo, Junsuke
Sato, Aki
Yamazaki, Motoyoshi
Hashidate, Hideki
Igarashi, Shuichi
Kakita, Akiyoshi - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>We report the clinical and autopsy features of a 65‐year‐old Japanese man who clinically exhibited overlap of both neuro‐Behçet's disease (NBD) and amyotrophic lateral sclerosis (ALS). The patient had a HLA‐B51 serotype, a recent history of uveitis and had suffered paraparesis, sensory and autonomic disturbance, frontal signs and tremor. A brain and spine MRI study revealed a longitudinally extensive thoracic cord (Th) lesion, but no apparent intracranial abnormalities. The lesion extended ventrally from Th4 to Th9, exhibiting low intensity on T1‐weighted images, high intensity on T2‐weighted and fluid‐attenuated inversion recovery images and gadolinium enhancement. The patient's upper and lower motor neuron signs and sensory disturbance worsened and he died 16 months after admission. At autopsy, the spinal cord and brain exhibited characteristic histopathological features of both NBD and ALS, including chronic destruction of the ventral thoracic white and gray matter, perivascular lymphocytic infiltration, binucleated neurons, lower and upper motor neuron degeneration, Bunina bodies and skein‐like inclusions. Although incidental coexistence of these rare disorders could occur in an individual, this case raises the possibility of a pathomechanistic association between NBD and ALS.</p> </abstract>
- Is Part Of:
- Neuropathology. Volume 34:Issue 2(2014)
- Journal:
- Neuropathology
- Issue:
- Volume 34:Issue 2(2014)
- Issue Display:
- Volume 34, Issue 2 (2014)
- Year:
- 2014
- Volume:
- 34
- Issue:
- 2
- Issue Sort Value:
- 2014-0034-0002-0000
- Page Start:
- 185
- Page End:
- 189
- Publication Date:
- 2013-09-30
- Subjects:
- Nervous system -- Diseases -- Periodicals
Nervous system -- Pathophysiology -- Periodicals
616.8047 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=neu ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/neup.12074 ↗
- Languages:
- English
- ISSNs:
- 0919-6544
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.513800
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3906.xml