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首页> 外文期刊>Annals of Indian Academy of Neurology >Leukoencephalopathy with intracranial calcifications and cysts in an adult: Case report and review of literature
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Leukoencephalopathy with intracranial calcifications and cysts in an adult: Case report and review of literature

机译:成人白内障伴颅内钙化和囊肿:病例报告及文献复习

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Leukoencephalopathy, intracranial calcifications, and cysts (LCC) is a very rare cerebral disorder, first described in 3 children in 1996. It has subsequently been reported in adults and children from Europe and America, but has not so far been reported from Asia. We report an adult patient with pathologically proven LCC from a tertiary care hospital in South India. He presented with features of ataxia and raised intracranial pressure. Magnetic resonance imaging of the brain showed multiple bilateral cerebral cystic lesions along with diffuse white matter lesions in the cerebral and cerebellar white matter, and computed tomography of brain showed multiple calcifications in the white matter and basal ganglia. A large right cerebellar cyst causing mass effect was surgically excised. Histopathologic features were consistent with earlier reports of LCC and showed Rosenthal fibers, angiomatous changes, and calcifications. Our report suggests that although it is rare, LCC has a global distribution.
机译:白细胞性脑病,颅内钙化和囊肿(LCC)是一种非常罕见的脑部疾病,于1996年首次在3名儿童中发现。随后在欧洲和美国的成年人和儿童中都有报道,但在亚洲尚未见报道。我们报告了南印度一家三级医院的一名经过病理证实的LCC的成年患者。他表现出共济失调和颅内压升高的特征。大脑的磁共振成像显示大脑和小脑白质中有多个双侧脑囊性病变以及弥漫性白质病变,而脑部CT扫描显示白质和基底神经节中有多个钙化。手术切除了引起肿块效应的右小脑大囊肿。组织病理学特征与早期LCC报道一致,并显示Rosenthal纤维,血管瘤改变和钙化。我们的报告表明,尽管LCC很少,但其分布在全球。

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