 |
 |

Amyotrophy in Prion Diseases
Bradford B. Worrall, MD;
Lewis P. Rowland, MD;
Steven S.-M. Chin, MD, PhD;
James A. Mastrianni, MD
Arch Neurol. 2000;57:33-38.
Amyotrophic lateral sclerosis was once thought to be caused by persistent viral infection, partly because some patients with transmissible Creutzfeldt-Jakob disease showed prominent amyotrophy. However, in the past 15 years there has been little interest in the amyotrophy in prion diseases, and the possible link to amyotrophic lateral sclerosis has been eschewed. We analyzed case reports of prion disease published after 1968 for evidence of amyotrophy. We defined amyotrophy as clinically evident fasciculation buttressed by electromyographic results in some cases. We sought evidence of motor neuron degeneration at autopsy. Prion disease was proved by transmissibility, immunohistochemistry demonstration of protease-resistant prion protein, or finding a mutation in the prion protein gene. Amyotrophy was noted in 27 patients: 13 with sporadic Creutzfeldt-Jakob disease, 2 with familial Creutzfeldt-Jakob disease, and 12 with Gerstmann-Sträussler-Scheinker disease. Of the 27, 23 showed clinical fasciculation and 10 had electromyographic evidence of denervation. The spinal cord was examined in 8 patients: 6 showed loss of motor neurons, 1 showed vacuolation of motor neurons, and 1 reported no abnormalities. Another 23 patients had typical histopathological characteristics but lacked molecular or biochemical proof of prion disease. The total number of patients with amyotrophy and proven prion disease that we identified was 50. This case review supports the belief that amyotrophy is occasionally a prominent feature of Creutzfeldt-Jakob disease and underscores the importance of documenting lower motor neuron function and the crucial role of examining the spinal cord at autopsy in cases of prion disease.
From the Departments of Neurology (Drs Worrall and Rowland) and Pathology (Neuropathology) (Dr Chin), Columbia University College of Physicians & Surgeons, New York, NY; and the Department of Neurology, University of Chicago School of Medicine, Chicago, Ill (Dr Mastrianni). Dr Worrall is now with the Department of Neurology, University of Virginia Health Systems, Charlottesville.
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
 |
Codistribution of Amyloid {beta} Plaques and Spongiform Degeneration in Familial Creutzfeldt-Jakob Disease With the E200K-129M Haplotype
Ghoshal et al.
Arch Neurol 2009;66:1240-1246.
ABSTRACT
| FULL TEXT
A Man with a Gait Disorder
Mast et al.
NEJM 2006;355:1740-1740.
FULL TEXT
Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease
Ishida et al.
J. Neurol. Neurosurg. Psychiatry 2005;76:325-329.
ABSTRACT
| FULL TEXT
Failure to detect enterovirus in the spinal cord of ALS patients using a sensitive RT-PCR method
Nix et al.
Neurology 2004;62:1372-1377.
ABSTRACT
| FULL TEXT
Aggregate Formation in Cu,Zn Superoxide Dismutase-related Proteins
Son et al.
J. Biol. Chem. 2003;278:14331-14336.
ABSTRACT
| FULL TEXT
Creutzfeldt-Jakob Disease With Amyotrophy and Demyelinating Polyneuropathy
Kovacs et al.
Arch Neurol 2002;59:1811-1814.
ABSTRACT
| FULL TEXT
Impairment of the Peripheral Nervous System in Creutzfeldt-Jakob Disease
Niewiadomska et al.
Arch Neurol 2002;59:1430-1436.
ABSTRACT
| FULL TEXT
Dementia, Amyotrophy, and Periodic Complexes on the Electroencephalogram: A Diagnostic Challenge
Esteban et al.
Arch Neurol 2001;58:1669-1672.
ABSTRACT
| FULL TEXT
Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family
Kovacs et al.
J. Neurol. Neurosurg. Psychiatry 2001;70:802-805.
ABSTRACT
| FULL TEXT
Amyotrophic Lateral Sclerosis
Rowland and Shneider
NEJM 2001;344:1688-1700.
FULL TEXT
|