Ruggieri Martino, Polizzi Agata, Catanzaro Stefano, Bianco Manuela Lo, Praticò Andrea D, Di Rocco Concezio
Unit of Rare Diseases of the Nervous System in Childhood, Department of Clinical and Experimental Medicine, Section of Pediatrics and Child Neuropsychiatry, University of Catania, Catania, Italy.
Chair of Pediatrics, Department of Educational Sciences, University of Catania, Catania, Italy.
Childs Nerv Syst. 2020 Oct;36(10):2571-2596. doi: 10.1007/s00381-020-04770-9. Epub 2020 Oct 13.
Neurocutaneous melanosis (NCM; MIM # 249400; ORPHA: 2481], first reported by the Bohemian pathologist Rokitansky in 1861, and now more precisely defined as neurocutaneous melanocytosis, is a rare, congenital syndrome characterised by the association of (1) congenital melanocytic nevi (CMN) of the skin with overlying hypertrichosis, presenting as (a) large (LCMN) or giant and/or multiple (MCMN) melanocytic lesions (or both; sometimes associated with smaller "satellite" nevi) or (b) as proliferative melanocytic nodules; and (2) melanocytosis (with infiltration) of the brain parenchyma and/or leptomeninges. CMN of the skin and leptomeningeal/nervous system infiltration are usually benign, more rarely may progress to melanoma or non-malignant melanosis of the brain. Approximately 12% of individuals with LCMN will develop NCM: wide extension and/or dorsal axial distribution of LCMN increases the risk of NCM. The CMN are recognised at birth and are distributed over the skin according to 6 or more patterns (6B patterns) in line with the archetypical patterns of distribution of mosaic skin disorders. Neurological manifestations can appear acutely in infancy, or more frequently later in childhood or adult life, and include signs/symptoms of intracranial hypertension, seizures/epilepsy, cranial nerve palsies, motor/sensory deficits, cognitive/behavioural abnormalities, sleep cycle anomalies, and eventually neurological deterioration. NMC patients may be symptomatic or asymptomatic, with or without evidence of the typical nervous system changes at MRI. Associated brain and spinal cord malformations include the Dandy-Walker malformation (DWM) complex, hemimegalencephaly, cortical dysplasia, arachnoid cysts, Chiari I and II malformations, syringomyelia, meningoceles, occult spinal dysraphism, and CNS lipoma/lipomatosis. There is no systemic involvement, or only rarely. Pathogenically, single postzygotic mutations in the NRAS (neuroblastoma RAS viral oncogene homologue; MIM # 164790; at 1p13.2) proto-oncogene explain the occurrence of single/multiple CMNs and melanocytic and non-melanocytic nervous system lesions in NCM: these disrupt the RAS/ERK/mTOR/PI3K/akt pathways. Diagnostic/surveillance work-ups require physical examination, ophthalmoscopy, brain/spinal cord magnetic resonance imaging (MRI) and angiography (MRA), positron emission tomography (PET), and video-EEG and IQ testing. Treatment strategies include laser therapy, chemical peeling, dermabrasion, and surgical removal/grafting for CMNs and shunt surgery and surgical removal/chemo/radiotherapy for CNS lesions. Biologically targeted therapies tailored (a) BRAF/MEK in NCM mice (MEK162) and GCMN (trametinib); (b) PI3K/mTOR (omipalisib/GSK2126458) in NMC cells; (c) RAS/MEK (vemurafenib and trametinib) in LCMNs cells; or created experimental NMC cells (YP-MEL).
神经皮肤黑素沉着症(NCM;MIM编号#249400;孤儿病编号:2481),由波希米亚病理学家罗基坦斯基在1861年首次报道,现在更精确地定义为神经皮肤黑素细胞增多症,是一种罕见的先天性综合征,其特征为:(1)皮肤先天性黑素细胞痣(CMN)伴有覆盖其上的多毛症,表现为(a)大的(LCMN)或巨大和/或多发(MCMN)黑素细胞病变(或两者兼有;有时伴有较小的“卫星”痣)或(b)增殖性黑素细胞结节;以及(2)脑实质和/或软脑膜的黑素细胞增多症(伴有浸润)。皮肤CMN和软脑膜/神经系统浸润通常为良性,很少会进展为黑色素瘤或脑的非恶性黑素沉着症。大约12%的LCMN患者会发展为NCM:LCMN的广泛扩展和/或背部轴向分布会增加NCM的风险。CMN在出生时即可识别,根据6种或更多模式(6B模式)分布于皮肤上,这与镶嵌性皮肤病的典型分布模式一致。神经学表现可在婴儿期急性出现,或更常见于儿童期或成年期后期,包括颅内高压、癫痫发作/癫痫、颅神经麻痹、运动/感觉缺陷、认知/行为异常、睡眠周期异常等体征/症状,最终出现神经功能恶化。NMC患者可能有症状或无症状,MRI检查可能有或无典型神经系统改变的证据。相关的脑和脊髓畸形包括丹迪-沃克畸形(DWM)复合体、半侧巨脑畸形、皮质发育异常、蛛网膜囊肿、Chiari I和II畸形、脊髓空洞症、脊膜膨出、隐匿性脊柱裂以及中枢神经系统脂肪瘤/脂肪瘤病。一般无全身受累,或仅偶尔出现。从发病机制上讲,NRAS(神经母细胞瘤RAS病毒癌基因同源物;MIM编号#164790;位于1p13.2)原癌基因中的单个合子后突变解释了NCM中单个/多个CMN以及黑素细胞和非黑素细胞神经系统病变的发生:这些突变会破坏RAS/ERK/mTOR/PI3K/akt信号通路。诊断/监测检查需要进行体格检查、眼底检查、脑/脊髓磁共振成像(MRI)和血管造影(MRA)、正电子发射断层扫描(PET)以及视频脑电图和智商测试。治疗策略包括针对CMN的激光治疗、化学剥脱、磨皮术以及手术切除/移植,针对中枢神经系统病变的分流手术以及手术切除/化疗/放疗。针对NCM小鼠(MEK162)和巨大先天性黑素细胞痣(GCMN)(曲美替尼)的BRAF/MEK;(b)NMC细胞中的PI3K/mTOR(奥米帕利/GSK2126458);(c)LCMNs细胞中的RAS/MEK(维莫非尼和曲美替尼);或创建的实验性NMC细胞(YP-MEL)进行生物靶向治疗。