Sutton B J, Tatter S B, Stanton C A, Mott R T
Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Clin Neuropathol. 2011 Jul-Aug;30(4):178-82. doi: 10.5414/np300363.
Leptomeningeal melanocytosis is a primary melanocytic lesion of the central nervous system that is characterized by diffuse melanocytic infiltration of the leptomeninges. It is seen almost exclusively in children with large congenital nevi and together the findings form a dermatologic syndrome known as neurocutaneous melanosis. We report a rare and atypical case of a 31-year-old adult male with no evident congenital melanocytic lesions who presented with neurologic symptoms and was found to have leptomeningeal melanocytosis. The brain biopsy demonstrated a conspicuous but benign-appearing melanocytic infiltrate that was discordant with the severity of the patient's symptoms. Ultimately, the patient was suspected to represent a case of former fruste neurocutaneous melanosis. Herein the relevant clinical and histopathologic features are discussed along with a brief review of the literature.
柔脑膜黑素细胞增多症是一种中枢神经系统的原发性黑素细胞病变,其特征为柔脑膜弥漫性黑素细胞浸润。几乎仅在患有巨大先天性痣的儿童中可见,这些表现共同构成一种称为神经皮肤黑素沉着症的皮肤病综合征。我们报告了一例罕见的非典型病例,一名31岁成年男性,无明显先天性黑素细胞病变,出现神经系统症状,经检查发现患有柔脑膜黑素细胞增多症。脑活检显示有明显但外观良性的黑素细胞浸润,这与患者症状的严重程度不一致。最终,该患者被怀疑为既往顿挫型神经皮肤黑素沉着症病例。本文讨论了相关的临床和组织病理学特征,并对文献进行了简要回顾。