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巨大先天性黑素细胞痣:神经无症状儿童的脑磁共振成像表现

Giant congenital melanocytic nevi: brain magnetic resonance findings in neurologically asymptomatic children.

作者信息

Frieden I J, Williams M L, Barkovich A J

机构信息

Department of Dermatology, University of California, School of Medicine, San Francisco.

出版信息

J Am Acad Dermatol. 1994 Sep;31(3 Pt 1):423-9. doi: 10.1016/s0190-9622(94)70204-7.

Abstract

BACKGROUND

Patients with giant or multiple congenital melanocytic nevi occasionally have leptomeningeal melanocytosis, also called neurocutaneous melanosis (NCM). Patients with symptomatic NCM usually have signs or symptoms of increased intracranial pressure and have a poor prognosis. Magnetic resonance (MR) imaging is sensitive in detecting melanin; several recent reports have described the MR findings in neurocutaneous melanosis.

OBJECTIVE

The aim of this study is to review the brain MR findings and their potential significance in a group of neurologically asymptomatic children with giant congenital melanocytic nevi at risk for the development of NCM.

METHODS

Retrospective review of patient charts and MR studies was performed.

RESULTS

Nine of the 20 patients evaluated had MR abnormalities: six had focal areas of high signal on T1-weighted images, strongly suggestive of melanosis, in one or multiple areas of the brain including the temporal lobes, cerebellum, pons, and medulla. One had a middle cranial fossa arachnoid cyst; another had a Chiari type I malformation of the brain. In one patient a crescentic enhancement over the right parietal region, probably from perinatal trauma, was absent on repeat MR 6 months later. In no case was thickening of the leptomeninges or spinal abnormalities noted.

CONCLUSIONS

NCM may be much more common than previously suspected in patients with giant congenital melanocytic nevi. The most common finding on MR appears to be T1 shortening in the cerebellum, temporal lobes, pons, and medulla, rather than evidence of leptomeningeal thickening. These findings may have implications for management of patients with giant CMN.

摘要

背景

患有巨大或多发性先天性黑素细胞痣的患者偶尔会出现软脑膜黑素沉着症,也称为神经皮肤黑素沉着症(NCM)。有症状的NCM患者通常有颅内压升高的体征或症状,预后较差。磁共振(MR)成像对检测黑色素很敏感;最近有几份报告描述了神经皮肤黑素沉着症的MR表现。

目的

本研究的目的是回顾一组有NCM发生风险的神经无症状的巨大先天性黑素细胞痣患儿的脑部MR表现及其潜在意义。

方法

对患者病历和MR研究进行回顾性分析。

结果

在评估的20例患者中,9例有MR异常:6例在T1加权图像上有高信号灶,强烈提示黑素沉着症,位于大脑的一个或多个区域,包括颞叶、小脑、脑桥和延髓。1例有中颅窝蛛网膜囊肿;另1例有Chiari I型脑畸形。1例患者右顶叶区域的新月形强化可能源于围产期创伤,6个月后复查MR时消失。无一例出现软脑膜增厚或脊柱异常。

结论

NCM在巨大先天性黑素细胞痣患者中可能比以前怀疑的更为常见。MR上最常见的表现似乎是小脑、颞叶、脑桥和延髓的T1缩短,而不是软脑膜增厚的证据。这些发现可能对巨大先天性黑素细胞痣患者的管理有影响。

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