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弥漫性间变性软脑膜少突胶质细胞瘤病,酷似神经结节病。

Diffuse anaplastic leptomeningeal oligodendrogliomatosis mimicking neurosarcoidosis.

作者信息

Leep Hunderfund Andrea N, Zabad Rana K, Aksamit Allen J, Morris Jonathan M, Meyer Fredric B, Thorell William E, Parisi Joseph E, Giannini Caterina

机构信息

Departments of Neurology (A.N.L.H., A.J.A.), Neurosurgery (F.B.M.), Radiology (J.M.M.), and Pathology (J.E.P., C.G.), Mayo Clinic College of Medicine, Rochester, MN; and the Department of Neurological Sciences (R.K.Z.) and the Division of Neurosurgery (W.E.T.), Nebraska Medical Center, Omaha.

出版信息

Neurol Clin Pract. 2013 Jun;3(3):261-265. doi: 10.1212/CPJ.0b013e318296f23d.

Abstract

Diffuse leptomeningeal oligodendrogliomatosis is a rare, frequently fatal CNS malignancy that most often affects children. Although potentially treatable with chemotherapy and radiation, the radiologic findings are nonspecific and pathologic confirmation of the diagnosis is difficult. We describe an adult patient whose initial presentation mimicked neurosarcoidosis. Despite extensive imaging abnormalities, 3 biopsies were required before the diagnosis of diffuse leptomeningeal oligodendrogliomatosis was confirmed.

摘要

弥漫性软脑膜少突胶质细胞瘤病是一种罕见的、通常致命的中枢神经系统恶性肿瘤,最常累及儿童。尽管可用化疗和放疗进行潜在治疗,但影像学表现不具特异性,诊断的病理确认很困难。我们描述了一名成年患者,其最初表现类似神经结节病。尽管有广泛的影像学异常,但在弥漫性软脑膜少突胶质细胞瘤病的诊断得到确认之前,需要进行3次活检。

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本文引用的文献

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Primary diffuse leptomeningeal gliomatosis.原发性弥漫性软脑膜胶质瘤病
Eur Neurol. 2009;62(1):16-22. doi: 10.1159/000216838. Epub 2009 May 4.

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