| Literature DB >> 24286527 |
Igor Paredes1, Jesus Esteban, Ana Ramos, Pedro Gonzalez, Juan José Rivas.
Abstract
Hirayama disease, or juvenile amyotrophy of distal upper extremity, is a benign, self-limiting cervical myelopathy consisting of selective unilateral weakness of the hand and forearm. The weakness slowly progresses until spontaneous arrest occurs within 5 years of onset. The condition predominantly affects Asian males and is thought to be secondary to spinal cord compression during neck flexion, because of a forward displacement of the posterior dural sac. The authors present what is to their knowledge the first reported case of a Caucasian male with a severe form of Hirayama disease, suffering from weakness of the leg as well as the forearm. An abnormal range of cervical flexion was observed at the C5-6 level. The patient was successfully treated by anterior cervical discectomy and fusion.Entities:
Mesh:
Year: 2013 PMID: 24286527 DOI: 10.3171/2013.10.SPINE13508
Source DB: PubMed Journal: J Neurosurg Spine ISSN: 1547-5646