Proteasa Adelina, Walton Myles Benjamin, Carrera Ines, Garosi Laurent S, Alcoverro Emili, Heyes Menai, Tauro Anna
frank Pet Surgeons., Leeds, UK.
Movement Referrals, Independent Veterinary Specialists, Preston Brook, UK.
JFMS Open Rep. 2023 Aug 2;9(2):20551169231186860. doi: 10.1177/20551169231186860. eCollection 2023 Jul-Dec.
A 1-year-old castrated male Maine Coon cat was referred because of a 1-week history of progressive spastic non-ambulatory paraparesis. An MRI examination of the thoracolumbar spine showed multiple lytic lesions, with the most aggressive one centred on the adjacent endplates of L1-L2 and its associated disc. Ventral new bone formation, L1 vertebral body shortening and mild dorsal displacement of the caudal aspect of L1 were noted. Contrast enhancement of both paravertebral soft tissue and extradural lesion was present. These findings were compatible with L1-L2 discospondylitis (DS), spinal epidural empyema (SEE), with secondary L1 pathological vertebral fracture, subluxation and spinal cord compression. CT of the thoracolumbar spine, abdomen and thorax confirmed these findings. The patient deteriorated to paraplegia with absent nociception, despite initial medical therapy. A right-sided L1-L2 hemilaminectomy and spinal decompression were then performed, followed by application of a unilateral construct comprising four smooth arthrodesis wires and polymethylmethacrylate (PMMA). S was isolated from both epidural material, intraoperatively sampled and blood culture. Antibiotic therapy was continued for 6 weeks, based on susceptibility results. The outcome was excellent, with a gradual improvement and complete neurological recovery at the 8-week postoperative check. Repeated spinal radiographs showed an intact apparatus and marked signs of vertebral fusion. At the 14-month follow-up examination, the cat remained free of clinical signs.
To the authors' knowledge, this is the first case report of SEE and DS in a cat that required surgical stabilisation. The outcome was still optimal, despite the rapid neurological deterioration.
一只1岁去势雄性缅因猫因进行性痉挛性非行走性双下肢轻瘫1周病史而被转诊。胸腰椎的MRI检查显示多个溶骨性病变,最具侵袭性的病变集中在L1-L2相邻终板及其相关椎间盘。可见腹侧新骨形成、L1椎体缩短以及L1尾侧轻度背侧移位。椎旁软组织和硬膜外病变均有对比增强。这些发现符合L1-L2椎间盘炎(DS)、脊髓硬膜外脓肿(SEE),伴有继发性L1病理性椎体骨折、半脱位和脊髓受压。胸腰椎、腹部和胸部的CT证实了这些发现。尽管进行了初始药物治疗,但患者仍恶化为截瘫且痛觉缺失。随后进行了右侧L1-L2半椎板切除术和脊髓减压,接着应用了由四根光滑融合钢丝和聚甲基丙烯酸甲酯(PMMA)组成的单侧固定装置。从术中采集的硬膜外材料和血培养中均分离出了S。根据药敏结果继续抗生素治疗6周。结果非常好,术后8周检查时逐渐改善且神经功能完全恢复。重复的脊柱X线片显示固定装置完整且有明显的椎体融合迹象。在14个月的随访检查中,这只猫没有临床症状。
据作者所知,这是首例需要手术稳定治疗的猫的SEE和DS病例报告。尽管神经功能迅速恶化,但结果仍然最佳。