Nomura T, Yamada T, Kobayashi T, Goto I
Department of Neurology, Faculty of Medicine, Kyushu University.
Rinsho Shinkeigaku. 1993 Apr;33(4):449-51.
A 71-year-old man with bilateral medial longitudinal fasciculus (MLF) syndrome and paralytic pontine exotropia caused by an infarction of the midbrain tegmentum was reported. He suddenly noticed a diplopia and gait disturbance, and visited our clinic. Neurological examination revealed that this right eye was slightly abducted in the primary position. On horizontal gaze, outwardbeating nystagmus of the abducted eyes was observed, bilaterally. The adduction of the bilateral eyes was severely disturbed and the abduction of the left eye was slightly restricted, while the convergence was normal. T2-weighted magnetic resonance imaging revealed high signal intensity area in the medial portion of the midbrain tegmentum, which indicated an infarction. Several cases showing bilateral MLF syndrome with exotropia have been reported, but a case whose lesion was shown in the midbrain has not been reported so far. The present case suggests that paramedian pontine reticular formation (PPRF) is not confined to pons but expands to midbrain.
报告了一名71岁男性,患有双侧内侧纵束(MLF)综合征及由中脑被盖梗死引起的麻痹性脑桥外斜视。他突然出现复视和步态障碍,并前来我院就诊。神经学检查发现,右眼在第一眼位时轻度外展。水平注视时,双侧外展眼均出现向外跳动性眼球震颤。双眼内收严重受限,左眼外展轻度受限,而集合正常。T2加权磁共振成像显示中脑被盖内侧部分有高信号强度区,提示梗死。此前已有数例双侧MLF综合征伴外斜视的病例报道,但病变位于中脑的病例尚未见报道。本病例提示脑桥旁正中网状结构(PPRF)不仅局限于脑桥,还扩展至中脑。