Fujiwara S, Sawamura Y, Kato T, Abe H, Katusima H
Department of Neurosurgery, University of Hokkaido, School of Medicine, Kita-ku, Sapporo, Japan.
J Neurol Neurosurg Psychiatry. 1997 Jun;62(6):652-4. doi: 10.1136/jnnp.62.6.652.
The authors report on female homozygous twins with idiopathic intracranial hypertension. At the age of 12 years, both twins simultaneously developed visual disturbances with photophobia. At the age of 19 years, an ophthalmological examination disclosed papilloedema in both their eyes. At the age of 22 years, a lumbar puncture showed raised CSF pressure over (200 mm H2O) in both twins. Their neurological and radiological examinations were extremely similar; both of them had severely impaired visual acuity and impaired visual field, bilateral optic nerve atrophy, intracranial hypertension, an enlarged and partial empty sella turcica, digital markings of the calvalium, and an enlarged frontal subarachnoid space. This is the first case report describing idiopathic intracranial hypertension occurring in homozygous twins.
作者报告了一对患有特发性颅内高压的女性同卵双胞胎。12岁时,这对双胞胎同时出现畏光导致的视觉障碍。19岁时,眼科检查发现她们双眼均有视乳头水肿。22岁时,腰椎穿刺显示双胞胎脑脊液压力均升高(超过200 mm H2O)。她们的神经学和影像学检查极为相似;两人均有严重视力受损和视野缺损、双侧视神经萎缩、颅内高压、蝶鞍增大及部分空蝶鞍、颅骨数字标记以及额叶蛛网膜下腔增宽。这是首例描述同卵双胞胎发生特发性颅内高压的病例报告。