Giant cell tumor of the occipital bone in a case of von Recklinghausen neurofibromatosis

被引：0

作者：

Opitz, H

Petersen, D

Heiss, E

Duffner, F

Meyermann, R

机构：

[1] UNIV TUBINGEN,DEPT NEUROPATHOL,D-72076 TUBINGEN,GERMANY

[2] UNIV TUBINGEN,DEPT NEURORADIOL,D-72076 TUBINGEN,GERMANY

来源：

CLINICAL NEUROPATHOLOGY | 1996年 / 15卷 / 04期

关键词：

giant cell tumor; NF1; skull; electron microscopy; immunohistochemistry;

D O I：

暂无

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Von Recklinghausen neurofibromatosis (NF1) is the most common hereditary syndrome predisposing to neoplasia. The most common symptomatic manifestation of NF1 is the plexiform neurofibroma. We describe the case of a patient with classical von Recklinghausen neurofibromatosis presenting with a giant cell tumor (GCT) of the occipital bone infiltrating a surrounding plexiform neurofibroma.

引用

页码：226 / 230

页数：5

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