Shoda Naoki, Anamizu Yorito, Yonezawa Naoko, Ishibashi Hideaki, Yamamoto Seizo
Orthopaedic Surgery Division, Yokohama Rosai Hospital, Yokohama City, Kanagawa, Japan.
Spine (Phila Pa 1976). 2005 May 1;30(9):E248-50. doi: 10.1097/01.brs.0000160996.82470.c0.
Case report.
To report a case of ossification of the posterior atlantoaxial membrane (PAAM) and ossification of the transverse ligament of the atlas (TAL).
Ossification of the PAAM and TAL are both very rare clinical entities. This is the first case involving ossification of both the PAAM and TAL with the development of cervical myelopathy.
Patient's history, physical examination, radiographic evaluation, surgical treatment, and outcome are examined. Relevant literature is also reviewed.
The patient's neurological symptoms significantly improved after posterior decompressive surgery.
Ossification of various parts of the spinal ligament have been reported previously. Among them, ossification of both the PAAM and TAL has never been reported previously and is thus extremely rare. Surgical intervention improved the neurological impairment.
病例报告。
报告1例寰枢后膜(PAAM)骨化和寰椎横韧带(TAL)骨化的病例。
PAAM骨化和TAL骨化均为非常罕见的临床病症。这是首例同时发生PAAM骨化和TAL骨化并伴有颈椎脊髓病的病例。
对患者的病史、体格检查、影像学评估、手术治疗及结果进行了检查。同时回顾了相关文献。
后路减压手术后患者的神经症状明显改善。
先前已有关于脊柱韧带各部位骨化的报道。其中,PAAM和TAL同时骨化此前从未有过报道,因此极为罕见。手术干预改善了神经功能障碍。