Lim S H, Wong M C, Puvan K
Singapore Med J. 1989 Aug;30(4):376-9.
4 cases of syringomyelia with type I Arnold Chiari malformation was seen presenting mainly with dissociated sensory loss, weakness of hands and upper motor neurone signs in the lower limbs. The first patient improved with posterior fossa decompression. The second and fourth patient appeared not to have improved after surgery, and the third case refused operation. One patient showed cord atrophy on myelogram presumably due to a collapse of the syrinx. One of the patients was unusual in that the syrinx extended down to segment T11. Magnetic resonance imaging of the posterior fossa and the cervical cord, to date, is the most useful procedure for diagnosis.
4例伴有Ⅰ型阿诺德-基亚里畸形的脊髓空洞症患者,主要表现为分离性感觉障碍、手部无力及下肢上运动神经元体征。首例患者经后颅窝减压术后病情改善。第二例和第四例患者术后未见改善,第三例患者拒绝手术。1例患者脊髓造影显示脊髓萎缩,推测系空洞塌陷所致。其中1例患者情况特殊,其空洞向下延伸至T11节段。迄今为止,后颅窝和颈髓的磁共振成像检查是最有用的诊断方法。