Tagawa T, Otani K, Futagi Y, Arai H, Mushiake S, Nakayama M, Morita Y
Division of Pediatric Neurology, Osaka Medical Center.
No To Hattatsu. 1994 Nov;26(6):518-21.
A girl aged 1 year and 2 months with hypomelanosis of Ito was reported. She suffered from intractable epileptic seizures since the second day after birth. Characteristic bizarre hypopigmented skin lesions were seen on her left shoulder and extended in a linear fashion to the flexion side of the left upper extremity. Brain MRI revealed diffuse enlargement of the left hemisphere, dilatation of the left lateral ventricle, and neuronal migration anomalies, indicating hemimegalencephaly. The types of her seizures were secondarily generalized or unilateral initially, followed by infantile spasms at 1.5 month. Around 4 months of age, frequent partial seizures appeared. Her seizures were intractable despite vigorous anticonvulsant therapy. As patients with hypomelanosis of Ito are frequently associated with neurological abnormalities, brain MRI studies were thought to be essential in detecting central nervous system anomalies, particularly in the presence of early onset intractable seizures.
报告了一名1岁2个月大患伊藤色素减退症的女孩。她自出生后第二天起就患有难治性癫痫发作。在她的左肩可见特征性的奇异色素减退性皮肤病变,并呈线状延伸至左上肢的屈侧。脑部磁共振成像显示左半球弥漫性增大、左侧脑室扩张以及神经元迁移异常,提示半侧巨脑症。她的癫痫发作类型最初为继发性全身性或单侧性,随后在1.5个月时出现婴儿痉挛症。在4个月大左右,频繁出现部分性癫痫发作。尽管进行了积极的抗惊厥治疗,她的癫痫发作仍难以控制。由于伊藤色素减退症患者常伴有神经异常,因此脑部磁共振成像研究被认为对于检测中枢神经系统异常至关重要,尤其是在存在早发性难治性癫痫发作的情况下。