Higgins R J, LeCouteur R A, Kornegay J N, Coates J R
Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, 95616, USA.
Acta Neuropathol. 1998 Jul;96(1):97-101. doi: 10.1007/s004010050865.
Eight Brittany Spaniel dogs, seven females and one male, between 7 and 14 years old presented with clinical neurological signs of spinocerebellar disease of about 6 months to 4 years duration. Clinically the dogs had a dramatic forward "saluting" movement of the thoracic limbs, hypermetria of the pelvic limbs, cerebellar ataxia and intention tremors. Terminally, dogs crawled in a crouched thoracic posture with neck extension. Lesions were confined to cerebellum, medulla oblongata and spinal cord. The most severe lesion was diffuse Purkinje cell loss with massive neurofilament accumulation in degenerating cells. There was some bilateral neuronal degeneration in the dorsal horns of the spinal cord and in the gracilis and cuneate nuclei. There was bilateral sporadic axonal degeneration in the dorsal columns and lateral and ventromedial areas of the spinal cord. The etiology of this syndrome was not determined.
8只不列塔尼猎犬,7只雌性,1只雄性,年龄在7至14岁之间,出现了持续约6个月至4年的脊髓小脑疾病临床神经学症状。临床上,这些犬的胸肢有剧烈的向前“敬礼”动作,盆腔肢有辨距过度、小脑性共济失调和意向性震颤。末期,犬以蹲伏的胸姿爬行,颈部伸展。病变局限于小脑、延髓和脊髓。最严重的病变是弥漫性浦肯野细胞丢失,变性细胞中有大量神经丝积聚。脊髓背角、薄束核和楔束核有一些双侧神经元变性。脊髓背柱以及脊髓外侧和腹内侧区域有双侧散发性轴突变性。该综合征的病因尚未确定。