Solitary Fibrous Tumor of the Thigh: A Patient Report

被引:0
|
作者
Yamaga, Kensaku [1 ]
Minamizaki, Takeshi [2 ]
Osaki, Mari [2 ]
Shomori, Kohei [1 ]
Ishiguro, Naoko [3 ]
Yoshida, Haruhiko [1 ]
Ito, Hisao [1 ]
机构
[1] Tottori Univ, Div Organ Pathol, Dept Pathol & Microbiol, Sch Med,Fac Med, Yonago, Tottori 6838503, Japan
[2] Natl Hosp Org, Dept Orthoped Surg, Yonago Med Ctr, Yonago, Tottori 6838518, Japan
[3] Tottori Univ, Dept Pathobiol Sci & Technol, Sch Hlth Sci, Fac Med, Yonago, Tottori 6838503, Japan
关键词
extremity; soft tissue tumor; solitary fibrous tumor;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We report a rare case of solitary fibrous tumor (SFT) within the thigh muscle. A 37-year-old woman noticed a painless mass in her left thigh, which had gradually enlarged. Computed tomography (CT) showed an intramuscular tumor and enhanced CT showed strong enhancement within the lesion. Magnetic resonance imaging revealed that the tumor measured 13.1 x 7.3 x 2.3 cm and was located within the sartorius muscle, with a clearly defined margin. Malignancy was suspected and the tumor was surgically resected. The tumor was characterized by a well-circumscribed lesion, and was composed of bland or short spindle cells, which were patterniess, with scattered thick collagen bundles, and variably gaping thin- or byalin-walled blood vessels. Immunohistochemically, the tumor cells were positive for vimentin, CD34, CD99 and focally, bcl-2. The tumor was subsequently diagnosed as an extrapleural SFT, which is classified into an intermediated (rarely metastasizing) category. Extrapleural SFT should be considered in the evaluation of soft tissue tumors in the extremities, although it may be rare.
引用
收藏
页码:77 / 82
页数:6
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