Department of Orthopaedics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, Japan.
Department of Rehabilitation Medicine, Japanese Red Cross Kyoto Daiichi Hospital, 15-749 Honmachi, Higashiyama-ku, Kyoto 605-0981, Japan.
Medicina (Kaunas). 2024 May 1;60(5):755. doi: 10.3390/medicina60050755.
Klippel-Feil syndrome (KFS) is characterized by the congenital fusion of the cervical vertebrae and is sometimes accompanied by anomalies in the craniocervical junction. In basilar invagination (BI), which is a dislocation of the dens in an upper direction, compression of the brainstem and cervical cord results in neurological defects and surgery is required. A 16-year-old boy diagnosed with KFS and severe BI presented with spastic tetraplegia, opisthotonus and dyspnea. CT scans showed basilar impression, occipitalization of C1 and fusion of C2/C3. MRI showed ventral compression of the medullocervical junction. Posterior occipitocervical reduction and fusion along with decompression were performed. Paralysis gradually improved postoperatively over 3 weeks. However, severe spasticity and opisthotonus persisted and intrathecal baclofen (ITB) therapy was initiated. Following this, opisthotonus disappeared and spasticity of the extremities improved. Rehabilitation therapy continued by controlling the dose of ITB. Five years after the surgery, self-propelled wheelchair driving was achieved and activities of daily life improved. The treatment strategy for patients with BI and congenital anomalies remains controversial. Posterior reduction and internal fixation using instrumentation were effective techniques in this case. Spasticity control achieved through a combination of surgery and ITB treatment enabled the amelioration of therapeutic efficacy of rehabilitation and the improvement of ADL.
克莱佩尔-菲尔综合征(KFS)的特征是颈椎先天性融合,有时伴有颅颈交界处异常。颅底凹陷症(BI)是齿状突向上移位,导致脑干和颈髓受压,引起神经功能缺陷,需要手术治疗。一名 16 岁的男孩患有 KFS 和严重的 BI,表现为痉挛性四肢瘫痪、角弓反张和呼吸困难。CT 扫描显示颅底凹陷、C1 枕骨化和 C2/C3 融合。MRI 显示颈髓腹侧受压。行后路枕颈减压融合术。术后 3 周,瘫痪逐渐改善。然而,严重的痉挛性和角弓反张持续存在,开始进行鞘内巴氯芬(ITB)治疗。此后,角弓反张消失,四肢痉挛性改善。通过控制 ITB 的剂量继续进行康复治疗。术后 5 年,实现了自行驱动轮椅,日常生活活动能力得到改善。对于 BI 和先天性异常的患者,治疗策略仍存在争议。后路减压和使用器械内固定是该病例有效的治疗技术。通过手术和 ITB 治疗相结合控制痉挛,提高了康复治疗的疗效,并改善了日常生活活动能力。