Two cases of solitary fibroustumor of the spinal cord are described.
2
Combining the histopathological and immunohistochemical features, the diagnosis was solitary fibroustumor.
3
The histological examination was malignant solitary fibroustumor of the kidney.
4
These results led to the diagnosis of solitary fibroustumor.
5
Solitary fibroustumor is a rare neoplasm of mesenchymal origin that usually affects the pleura.
6
Subsequent pathologic examination of the resected tissue confirmed that the tumor was calcifying fibroustumor.
7
A solitary fibroustumor (SFT) originating in the pancreas is rare.
8
Calcifying fibroustumor is a benign fibroustumor.
9
Infantile myofibromatosis (IM) is the most common benign fibroustumor of soft tissues affecting young children.
10
Thus, TERT promoter mutations in solitary fibroustumor influence gene expression and are associated with adverse patient outcome.
11
The authors report an unusual intra- and extramedullary location for a solitary fibroustumor of the cervical spine.
12
Ingleby describes a case of fibroustumor of the uterus terminating fatally, but not until three weeks after delivery.
13
Solitary fibroustumor is a spindle cell tumor deriving from mesenchymal cells that arises most commonly in the pleura.
14
Integrating TERT promoter mutational status with existing multivariable risk-prediction models might improve risk prediction in patients with solitary fibroustumor.
15
The histological as well as the immunohistochemical examination revealed the mass to be a solitary fibroustumor of the pleura.
16
Solitary fibroustumor (SFT) is rare mesenchymal neoplasm that has been originally and most often documented in the pleura.