Mesenchymal orbital tumors

被引：1
作者：
Civit, T. [1 ]
Klein, O. [1 ]
Freppel, S. [1 ]
Baylac, F. [2 ]
机构：
[1] CHU Nancy, Hop Cent, Dept Neurochirurg, F-54000 Nancy, France
[2] Cabinet Pathol, F-16000 Angouleme, France
来源：
NEUROCHIRURGIE | 2010年 / 56卷 / 2-3期
关键词：
Orbital fibrous tissue tumor; Orbital mesenchymal tumor; Fibrous histiocytoma; Solitary fibrous tumor; Leiomyoma; Leiomyosarcoma; Liposarcoma; SOLITARY FIBROUS TUMOR; OF-THE-LITERATURE; GIANT-CELL ANGIOFIBROMA; UNILATERAL PROPTOSIS; PRIMARY LIPOSARCOMA; NODULAR FASCIITIS; RHABDOID TUMOR; MRI FINDINGS; LEIOMYOSARCOMA; LEIOMYOMA;
D O I：
10.1016/j.neuchi.2010.02.007
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Mesenchymal tumors grow from pluripotent mesenchymal cells that form the soft orbital tissue. Primary tumors of the orbital walls are discussed in another section. Tumors from muscle and adipose tissue are rare or exceptional, except rhabdomyosarcoma, described in the section dedicated to pediatric tumors. Most frequent tumors are fibrous histiocytomas and solitary fibrous tumors, which often have a retrobulbar location. Fibrous histiocytoma is benign in only 65% of cases. Fibrous solitary tumor is now better known (Ag CD34): this tumor is generally benign but frequently recurs. (C) 2010 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码：158 / 164
页数：7
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