Intravascular Papillary Endothelial Hyperplasia of the Central Nervous System(Four Case Reports)

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概要

• 論文の詳細を見る

• Four rare cases of intracranial intravascular papillary endothelial hyperplasia (IPEH) manifesting as cranial nerve disturbances occurred in 16-, 18-, 24-, and 28-year-old females. Magnetic resonance imaging showed all lesions as isointense with strong enhancement on T_1-weighted images, and as hyperintense on T_2-weighted images. All lesions were removed via craniotomies. Histological examination found vascular structures and papillary spaces lined with endothelial cells showing immunoreactivity for CD31. Complete removal was curative in two cases, whereas incomplete removal resulted in cure in one case and residual deficits in one case. latrogenic deficits should be avoided in IPEH treatment by surgery. Differentiation from neoplasm such as angiosarcoma depends on histological characteristics.

• 日本脳神経外科学会の論文
• 2004-06-15

著者

• Dalbasti Tayfun

  Department Of Neurosurgery Ege University Faculty Of Medicine

• Cagli Sedat

  Department Of Neurosurgery Ege University Faculty Of Medicine

• Demirtas Eren

  Department Of Neurosurgery Ege University Faculty Of Medicine

• OKTAR Nezih

  Department of Neurosurgery, Ege University Faculty of Medicine

• ISLEKEL Sertac

  Department of Neurosurgery, Ege University Faculty of Medicine

• OZDAMAR Nurcan

  Department of Neurosurgery, Ege University Faculty of Medicine

• Oktar Nezih

  Department Of Neurosurgery Ege University Faculty Of Medicine

• Ozdamar Nurcan

  Department Of Neurosurgery Ege University Faculty Of Medicine

• Islekel Sertac

  Department Of Neurosurgery Ege University Faculty Of Medicine

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• Intravascular Papillary Endothelial Hyperplasia of the Central Nervous System(Four Case Reports)
• Infantile polymyositis with normal serum creatine kinase level
• Pigmented ependymoma with signet-ring cells and Rosenthal fibers : A rare variant of ependymoma

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