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现报道1例儿童神经纤维瘤Ⅰ型(NF—Ⅰ)患者并发闭塞性脑血管病。病例黑人女孩,年龄2岁8个月,发育迟缓。已确诊为NF—Ⅰ并且有确定的家族史。突然发生左侧肢体力弱和不能行走。体检:身体有多处牛奶咖啡样斑和腹部雀斑。神经系统检查:左侧轻偏瘫和中枢性面瘫,左腱反射亢进。无镰状细胞病或高血压病史。脑CT示右内囊和右额叶有陈旧性梗阻灶及在右运动
Is reported in 1 cases of children with neurofibromatosis type 1 (NF-Ⅰ) patients complicated by occlusive cerebrovascular disease. Case black girl, age 2 years and 8 months, stunting. Has been diagnosed with NF-Ⅰ and has a confirmed family history. A sudden left limb weakness and can not walk. Physical examination: The body has a number of milk-like coffee-like spots and abdomen freckles. Neurological examination: Left hemiparesis and central paralysis, left tendon hyperreflexia. No history of sickle cell disease or hypertension. Brain CT showed the right internal capsule and right frontal obstruction with obstruction and right in the right movement