Jain Puneet, Chakrabarty Biswaroop, Kumar Atin, Gupta Neerja, Kabra Madhulika, Gulati Sheffali
Division of Pediatric Neurology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Department of Radio-Diagnosis, JPNA Trauma Centre, All India Institute of Medical Sciences, New Delhi, India.
J Child Neurol. 2014 Jun;29(6):846-9. doi: 10.1177/0883073813485432. Epub 2013 Apr 25.
Encephalocraniocutaneous lipomatosis is a rare neurocutaneous syndrome characterized by classical cutaneous and ocular lesions with central nervous system anomalies. We describe an infant with classical encephalocraniocutaneous lipomatosis characterized by probable naevus psiloliparus, frontal subcutaneous lipomas, ocular limbal dermoids and arachnoid cysts, and ventriculomegaly. He also had giant congenital nevus with leptomeningeal melanosis. This case represents a rare association between encephalocraniocutaneous lipomatosis and neurocutaneous melanosis.
脑颜面皮肤脂肪瘤病是一种罕见的神经皮肤综合征,其特征为典型的皮肤和眼部病变以及中枢神经系统异常。我们描述了一名患有典型脑颜面皮肤脂肪瘤病的婴儿,其特征包括可能的单纯性脂肪瘤痣、额部皮下脂肪瘤、眼缘皮样囊肿和蛛网膜囊肿,以及脑室扩大。他还患有巨大先天性痣伴软脑膜黑素沉着症。该病例代表了脑颜面皮肤脂肪瘤病与神经皮肤黑素沉着症之间罕见的关联。