Solitary fibrous tumor of the central nervous system: report of 2 cases and review of literature

被引:0
|
作者
Wen, Ge [1 ]
Li, Meifang [1 ]
Xu, Lijun [2 ]
Hu, Peiqian [1 ]
Liao, Xin [3 ]
Lin, Chuang [4 ]
Zhao, Liang [2 ,4 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Imaging Ctr, Guangzhou, Guangdong, Peoples R China
[2] Southern Med Univ, Sch Basic Med Sci, Dept Pathol, Guangzhou, Guangdong, Peoples R China
[3] Southern Med Univ, Nanfang Hosp, Dept Radiol, Guangzhou, Guangdong, Peoples R China
[4] Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou, Guangdong, Peoples R China
关键词
Solitary fibrous tumor; central nervous system; immunohistochemistry; magnetic resonance imaging; CD34; TERM-FOLLOW-UP; HISTOPATHOLOGICAL FEATURES; MENINGES;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Solitary fibrous tumors (SFTs) rarely occur in the central nervous system (CNS). Involvement of the and pineal gland is rarely recorded. Herein, we represent 2 cases of SFTs and firstly report SFT of the pineal gland. Cranial MR imaging showed isointense to hypointense signal intensity, and marked enhancement. Microscopically, the tumors showed characteristic "patternless-pattern" architecture. Elongated tumour cells formed fascicles alternating with hypocellular densely collagenous stroma. Immunohistochemistry for CD34, BCL2, and CD99 favors the definitive diagnosis of SFT. It is difficult to predict prognosis in patients with intraventricular SFT. In general, complete surgical resection may offer the best chance of a favorable clinical outcome.
引用
收藏
页码:3444 / 3448
页数:5
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