Lee Cheong H, Casey Adrian T H, Allibone James B, Chelvarajah Ramesh
The National Hospital for Neurology and Neurosurgery, Queen Square, London; and Spinal Surgery Unit, Royal National Orthopaedic Hospital, Stanmore, United Kingdom.
J Neurosurg Spine. 2006 Dec;5(6):550-3. doi: 10.3171/spi.2006.5.6.550.
The authors describe a previously unreported clinical sign that may indicate the onset of significant compression of the medulla oblongata in cases of craniovertebral junction abnormalities. This 17-year-old boy presented with mild bilateral leg weakness. Imaging studies revealed severe basilar invagination and a marked Chiari malformation. While awaiting surgery, his tongue developed an involuntary constant protrusion-intrusion repetitive motion. The onset of this so-named "trombone tongue" sign was followed shortly afterward by rapidly progressive spastic tetraparesis. After the authors performed a transmaxillary clivectomy, foramen magnum decompression, and occipitocervical fusion, they noted that the abnormal tongue motion promptly resolved and the tetraparesis gradually improved. The authors discuss their current understanding of the central control of tongue movements and present a hypothesis on the pathogenesis of trombone tongue based on the neuroanatomical basis of another abnormal tongue movement sign, lingual myoclonus.
作者描述了一种先前未报道的临床体征,该体征可能表明颅颈交界区异常病例中延髓受到显著压迫的开始。这名17岁男孩表现为轻度双侧腿部无力。影像学检查显示严重的基底凹陷和明显的Chiari畸形。在等待手术期间,他的舌头出现了不自主的持续伸出-缩回重复运动。这种所谓的“长号舌”体征出现后不久,迅速进展为痉挛性四肢轻瘫。作者进行经上颌斜坡切除术、枕骨大孔减压术和枕颈融合术后,他们注意到异常的舌头运动迅速消失,四肢轻瘫逐渐改善。作者讨论了他们目前对舌头运动中枢控制的理解,并基于另一种异常舌头运动体征——舌肌阵挛的神经解剖学基础,提出了长号舌发病机制的假说。