Rohdin Cecilia, Karlstam Erika, Jäderlund Karin Hultin, Shelton G Diane
Albano Small Animal Hospital, Rinkebyvägen 23, SE-182 36 Danderyd, Sweden.
J Feline Med Surg. 2010 Mar;12(3):237-40. doi: 10.1016/j.jfms.2010.01.007.
This report describes a kitten with paraplegia and extensor rigidity of the pelvic limbs associated with motor neuron loss and chronic denervation of skeletal muscle. Persistent skeletal muscle atrophy and degeneration had resulted in immobile stifle and hock joints and severe pelvic limb rigidity consistent with a neurogenic form of arthrogryposis. Both pelvic limbs were equally affected and the kitten showed no signs of pain.
Electromyography identified spontaneous activity in the pelvic limbs. Muscle and peripheral nerve biopsies showed pathology consistent with denervation. On necropsy, 3 weeks after admittance, severe degenerative changes including axonal necrosis and myelin degeneration were confirmed in the lumbar spinal cord.
There are very few descriptions of feline motor neuron degeneration in the literature and obtaining an ante-mortem diagnosis is difficult. Although an inherited disorder cannot be ruled out, a condition acquired congenitally in utero or postnatally was suspected in this case.
本报告描述了一只患有截瘫且骨盆肢体伸肌僵硬的小猫,伴有运动神经元丧失和骨骼肌慢性失神经支配。持续性骨骼肌萎缩和变性导致膝关节和跗关节无法活动,以及严重的骨盆肢体僵硬,符合神经源性关节挛缩症的表现。双侧骨盆肢体均受到同等程度影响,小猫未表现出疼痛迹象。
肌电图检查发现骨盆肢体有自发活动。肌肉和周围神经活检显示的病理变化与失神经支配相符。入院3周后尸检证实,腰椎脊髓出现严重的退行性变化,包括轴突坏死和髓鞘变性。
文献中关于猫运动神经元变性的描述非常少,生前诊断困难。尽管不能排除遗传性疾病,但本病例怀疑是在子宫内或出生后先天性获得的疾病。