Malignant giant cell tumor in the left upper arm soft tissue of an adolescent: A case report

被引:5
|
作者
Huang, Wen-Peng [1 ]
Zhu, Li-Na [1 ]
Li, Rui [1 ]
Li, Li-Ming [1 ]
Gao, Jian-Bo [1 ]
机构
[1] Zhengzhou Univ, Dept Radiol, Affiliated Hosp 1, 1 East Jianshe Rd, Zhengzhou 450052, Henan, Peoples R China
关键词
Bone scan; Giant cell tumor; Soft tissue; Tomography; X-ray computed; Magnetic resonance imaging; Case report;
D O I
10.12998/wjcc.v9.i15.3704
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Giant cell tumor of soft tissue (GCT-ST) is an extremely rare low-grade soft tissue tumor that is originates in superficial tissue and rarely spreads deeper. GCT-ST has unpredictable behavior. It is mainly benign, but may sometimes become aggressive and potentially increase in size within a short period of time. CASE SUMMARY A 17-year-old man was suspected of having a fracture, based on radiography following left shoulder trauma. One month later, the swelling of the left shoulder continued to increase and the pain was obvious. Computed tomography (CT) revealed a soft tissue mass with strip-like calcifications in the left shoulder. The mass invaded the adjacent humerus and showed an insect-like area of destruction at the edge of the cortical bone of the upper humerus. The marrow cavity of the upper humerus was enlarged, and a soft tissue density was seen in the medullary cavity. Thoracic CT revealed multiple small nodules beneath the pleura of both lungs. A bone scan demonstrated increased activity in the left shoulder joint and proximal humerus. The mass showed mixed moderate hypointensity and hyperintensity on T1-weighted images, and mixed hyperintensity on T2-weighted fat-saturated images. The final diagnosis of GCT-ST was confirmed by pathology. CONCLUSION GCT-STs should be considered in the differential diagnosis of soft tissue tumors and monitored for large increases in size.
引用
收藏
页码:3704 / 3710
页数:8
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