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伴有神经皮肤黑素沉着症的肢体巨大先天性黑素痣。

Large congenital melanotic nevi in an extremity with neurocutaneous melanocytosis.

作者信息

Becher Oren J, Souweidane Mark, Lavi Ehud, Kramer Kim, Lis Eric, Marghoob Ashfaq A, Khakoo Yasmin

机构信息

Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, USA.

出版信息

Pediatr Dermatol. 2009 Jan-Feb;26(1):79-82. doi: 10.1111/j.1525-1470.2008.00828.x.

Abstract

A 14-day-old boy presented with a large congenital melanocytic nevus over his left thigh with approximately 17 satellite nevi distributed over the rest of his skin surface. Six weeks later, he developed generalized tonic-clonic seizures and additional satellite nevi became apparent (n > 20). A subsequent brain magnetic resonance imaging demonstrated right temporal T1 hyperintense signal abnormality. At 4 months of age the patient underwent a lumbar puncture that was normal without evidence of melanocytes or tumor. Nevertheless, a few days later he underwent resection of his right medial temporal lesion which demonstrated melanocytosis in the temporal lobe as well as melanocytosis in subependymal areas in other parts of the brain and ventricles, confirming the suspected diagnosis of neurocutaneous melanocytosis. Our case supports previous studies that conclude that the number of satellite nevi is a greater predictor of neurocutaneous melanocytosis than is the location of large congenital melanocytic nevus. In our case, cerebrospinal fluid studies were not reliable even in the face of florid neurocutaneous melanocytosis involving the leptomeninges and ventricles.

摘要

一名14天大的男婴,左大腿有一个巨大先天性黑素细胞痣,其皮肤表面其他部位还有约17个卫星痣。六周后,他出现全身性强直阵挛发作,且又有明显的卫星痣出现(超过20个)。随后的脑部磁共振成像显示右侧颞叶T1高信号异常。在4个月大时,患者接受了腰椎穿刺,结果正常,未发现黑素细胞或肿瘤迹象。然而,几天后他接受了右侧颞叶内侧病变切除术,结果显示颞叶有黑素细胞增多,大脑其他部位和脑室的室管膜下区域也有黑素细胞增多,证实了神经皮肤黑素细胞增多症的疑似诊断。我们的病例支持先前的研究结论,即卫星痣的数量比巨大先天性黑素细胞痣的位置更能预测神经皮肤黑素细胞增多症。在我们的病例中,即使面对累及软脑膜和脑室的明显神经皮肤黑素细胞增多症,脑脊液检查也不可靠。

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