Iizuka Takahiro, Sakai Fumihiko, Ide Toshimitsu, Miyakawa Saori, Sato Mayumi, Yoshii Shintaro
Department of Neurology, School of Medicine, Kitasato University, 1-15-1 Kitasato, Sagamihara, Kanagawa, 228-8555, Japan.
J Neurol Sci. 2007 Jun 15;257(1-2):126-38. doi: 10.1016/j.jns.2007.01.040. Epub 2007 Feb 21.
Ischemic vascular hypothesis as a causative role in the pathogenesis of stroke-like episodes in MELAS remains to be debated.
This study consisted of two parts. Part 1 is a clinicoradiological study during acute stage of 18 consecutive stroke-like episodes in six patients with MELAS. Part 2 is a SPECT study to assess the regional cerebrovascular reactivity (rCVR) to acetazolamide during chronic stage in five patients with MELAS.
Headache and epileptic seizure were the most common presenting symptoms. Unique features of acute stroke-like lesions included progressive spread of cortical lesions with vasogenic edema, focal periodic epileptiform discharges, focal hyperperfusion, and cortical laminar necrosis during subacute stage. During chronic stage, SPECT showed hypoperfusion in non-affected occipital cortex in three patients as well as in previously affected regions in four. The rCVR was preserved in three patients, focally impaired in one, and extensively impaired in one, but relatively preserved in the occipital cortex in all patients.
Stroke-like episodes could be non-ischemic neurovascular events initiated by neuronal hyperexcitability. Once neuronal hyperexcitability develops in a focal brain region, epileptic activities depolarize adjacent neurons, leading to a propagation of epileptic activities into the surrounding cortex, and resulting in energy imbalance. The mechanisms for neuronal hyperexcitability remain to be elucidated.
缺血性血管假说在MELAS(线粒体脑肌病伴乳酸血症和卒中样发作)卒中样发作的发病机制中作为一个致病因素仍存在争议。
本研究包括两个部分。第一部分是对6例MELAS患者连续18次卒中样发作急性期的临床放射学研究。第二部分是对5例MELAS患者慢性期进行的单光子发射计算机断层扫描(SPECT)研究,以评估乙酰唑胺对局部脑血管反应性(rCVR)的影响。
头痛和癫痫发作是最常见的首发症状。急性卒中样病变的独特特征包括皮质病变伴血管源性水肿的进行性扩散、局灶性周期性癫痫样放电、局灶性血流灌注过多以及亚急性期的皮质层状坏死。在慢性期,SPECT显示3例患者未受影响的枕叶皮质以及4例患者先前受影响的区域存在灌注不足。3例患者的rCVR得以保留,1例患者局部受损,1例患者广泛受损,但所有患者的枕叶皮质rCVR相对保留。
卒中样发作可能是由神经元过度兴奋引发的非缺血性神经血管事件。一旦在局灶性脑区出现神经元过度兴奋,癫痫活动会使相邻神经元去极化,导致癫痫活动扩散至周围皮质,进而导致能量失衡。神经元过度兴奋的机制仍有待阐明。