Spinal muscular atrophy combined with sporadic olivopontocerebellar atrophy.

Spinal muscular atrophy combined with sporadic olivopontocerebellar atrophy.

【文献出处】Clin Neurol Neurosurg. 2008 Sep;110(8):855-8. Epub 2008 Jul 30.

【作者名】Luo W, Ouyang Z, Guo Y, Chen Y, Ding M.

【作者单位】Department of Neurology, Second Affiliated Hospital, School of Medicine, Zhejiang University, No. 88 Jiefang Road, Hangzhou City 310009, Zhejiang Province, China.

【摘要】The combination of spinal muscular atrophy (SMA) with a variety of neural and extraneural defects, particularly pontocerebellar hypoplasia, has been reported. To date, all of the reported SMA with pontocerebellar hypoplasia was from infants; however, here we report a SMA with sporadic olivopontocerebellar atrophy (sOPCA) in an adult patient. The 68-year-old male patient displayed various clinical symptoms including progressive proximal muscle weakness, muscle atrophy and muscle fasciculation with a long course of disease. EMG demonstrated that amyotrophy was due to the impairment of lower motor neurons. The clinical symptoms and the EMG were consistent with the diagnosis of SMA. The presence of cerebellar ataxia, limb tremors, muscle atrophy and weakness in the patient led to the diagnosis of sOPCA that was confirmed by the MRI results. To our knowledge, this is the first case report of combination of SMA with sOPCA in an adult. It is yet unclear whether there is a common pathogenesis between the two diseases.