Mari Lorenzo, Shelton G Diane, De Risio Luisa
Neurology/ Neurosurgery Service, Centre for Small Animal Studies, Animal Health Trust, Newmarket, UK.
Department of Pathology, School of Medicine, University of California, San Diego, CA, USA.
JFMS Open Rep. 2016 Feb 10;2(1):2055116916630335. doi: 10.1177/2055116916630335. eCollection 2016 Jan-Jun.
A 6-year-old female spayed Birman cat presented with a history of weight loss, stiff and short-strided gait in the pelvic limbs and reluctance to jump, progressing to non-ambulatory tetraparesis over 6 weeks. Poor body condition, dehydration and generalised muscle wastage were evident on general examination. Neurological examination revealed mildly depressed mental status, non-ambulatory flaccid tetraparesis and severely decreased proprioception and spinal reflexes in all four limbs. The neuroanatomical localisation was to the peripheral nervous system. Haematology, feline immunodeficiency virus/feline leukaemia virus serology, serum biochemistry, including creatine kinase and thyroxine, thoracic radiographs and abdominal ultrasound did not reveal significant abnormalities. Electromyography revealed fibrillation potentials and positive sharp waves in axial and appendicular muscles. Decreased motor conduction velocities and compound muscle action potential amplitudes were detected in ulnar and sciatic-tibial nerves. Residual latency was increased in the sciatic-tibial nerve. Histologically, several intramuscular nerve branches were depleted of myelinated fibres and a few showed mononuclear infiltrations. serology titres were compatible with active toxoplasmosis. Four days after treatment initiation with oral clindamycin the cat recovered the ability to walk. serology titres and neurological examination were normal after 11 and 16 weeks, respectively. Clindamycin was discontinued after 16 weeks. One year after presentation the cat showed mild relapse of clinical signs and seroconversion, which again resolved following treatment with clindamycin.
To our knowledge, this is the first report of distal polyneuropathy associated with toxoplasmosis in a cat. This case suggests the inclusion of toxoplasmosis as a possible differential diagnosis for acquired polyneuropathies in cats.
一只6岁已绝育的缅甸猫,出现体重减轻、盆腔肢体步态僵硬且步幅短以及不愿跳跃的病史,在6周内逐渐发展为四肢不能行走的轻瘫。全身检查发现身体状况差、脱水和全身肌肉萎缩。神经学检查显示精神状态轻度抑郁、四肢不能行走的弛缓性轻瘫以及所有四肢的本体感觉和脊髓反射严重减退。神经解剖定位为外周神经系统。血液学检查、猫免疫缺陷病毒/猫白血病病毒血清学检查、血清生化检查(包括肌酸激酶和甲状腺素)、胸部X光片和腹部超声均未发现明显异常。肌电图显示轴性和附属肌肉出现纤颤电位和正锐波。在尺神经和坐骨-胫神经中检测到运动传导速度降低和复合肌肉动作电位幅度减小。坐骨-胫神经的残余潜伏期增加。组织学检查显示,几条肌内神经分支的有髓纤维减少,少数有单核细胞浸润。血清学滴度与活动性弓形虫病相符。开始口服克林霉素治疗4天后,猫恢复了行走能力。11周和16周后,血清学滴度和神经学检查分别恢复正常。16周后停用克林霉素。就诊一年后,猫出现临床症状轻度复发和血清学转换,但再次用克林霉素治疗后症状又得到缓解。
据我们所知,这是猫中与弓形虫病相关的远端多发性神经病的首例报告。该病例提示应将弓形虫病纳入猫获得性多发性神经病的可能鉴别诊断中。