University of Cantabria, Service of Neurology, University Hospital "Marqués de Valdecilla (IDIVAL)", Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), Santander, Spain.
J Neurol Sci. 2017 Nov 15;382:1-9. doi: 10.1016/j.jns.2017.09.017. Epub 2017 Sep 13.
Pathological studies of early Guillain-Barré syndrome (GBS), defined as of 10days of disease onset, are scanty making it difficult to interpret the physiopathology of clinical and electrophysiological features. In 1949, Webb Haymaker and James Kernohan reported 50 clinico-pathological studies of fatal GBS cases, 32 of them having died between days 2 and 10 after onset. They established that the brunt of initial lesions, consisting of endoneurial oedema interpreted as degenerative, relied on spinal nerves. That this oedema was inflammatory was soon thereafter recognized. Two decades later, however, the pathogenic role of endoneurial oedema was disputed. In experimental allergic neuritis, considered an animal model of GBS, the initial lesion appearing on day 4 post-inoculation is marked inflammatory oedema in the sciatic nerve and lumbosacral nerve roots. Additional detailed clinico-pathological studies corroborated that the appearance of epi-perineurium at the subarachnoid angle, where anterior and posterior roots join to form the spinal nerve, is a pathological hotspot in early GBS, there developing inflammatory oedema, incipient demyelination and endoneurial ischemic zones with axonal degeneration. Furthermore, nerve ultrasonography has demonstrated predominant spinal nerve changes in early GBS, either demyelinating or axonal. Other outstanding Haymaker and Kernohan's contributions were to clarify the complex nosology of the syndrome bringing under the same rubric Landry's paralysis, acute febrile polyneuritis and GBS, and critically analyzing GBS exclusion criteria by then prevailing. It is concluded that the authors' legacy remains as relevant as ever.
早期吉兰-巴雷综合征(GBS)的病理研究(定义为发病后 10 天内)很少,这使得难以解释临床和电生理特征的病理生理学。1949 年,Webb Haymaker 和 James Kernohan 报告了 50 例致命 GBS 病例的临床病理研究,其中 32 例在发病后第 2 天至第 10 天死亡。他们证实,最初病变的主要部分,由被解释为退行性的神经内膜水肿组成,依赖于脊神经。此后不久,人们很快认识到这种水肿是炎症性的。然而,二十年后,神经内膜水肿的致病作用受到了争议。在实验性过敏性神经炎中,被认为是 GBS 的动物模型,在接种后第 4 天出现的最初病变是坐骨神经和腰骶神经根明显的炎症性水肿。其他详细的临床病理研究证实,蛛网膜下腔角处的外膜出现(前根和后根连接形成脊神经的部位)是早期 GBS 的一个病理热点,在那里会出现炎症性水肿、早期脱髓鞘和神经内膜缺血区伴轴突变性。此外,神经超声检查已经证明,早期 GBS 中主要发生脊神经变化,无论是脱髓鞘还是轴突性的。Haymaker 和 Kernohan 的其他杰出贡献是阐明了该综合征的复杂分类学,将 Landry 瘫痪、急性发热性多神经炎和 GBS 归入同一范畴,并对当时流行的 GBS 排除标准进行了批判性分析。总之,作者的遗产仍然与以往一样重要。