Desmoid tumors represent a particular type of fibrousneoplasms with a higher prevalence in females.
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Desmoid tumors are rare, benign fibroblastictumors that are locally infiltrative and can cause extensive morbidity by destruction of adjacent vital structures.
Uso de fibrous tumor en inglés
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Two cases of solitary fibroustumor of the spinal cord are described.
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Combining the histopathological and immunohistochemical features, the diagnosis was solitary fibroustumor.
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The histological examination was malignant solitary fibroustumor of the kidney.
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These results led to the diagnosis of solitary fibroustumor.
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Solitary fibroustumor is a rare neoplasm of mesenchymal origin that usually affects the pleura.
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Subsequent pathologic examination of the resected tissue confirmed that the tumor was calcifying fibroustumor.
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A solitary fibroustumor (SFT) originating in the pancreas is rare.
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Calcifying fibroustumor is a benign fibroustumor.
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Infantile myofibromatosis (IM) is the most common benign fibroustumor of soft tissues affecting young children.
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Thus, TERT promoter mutations in solitary fibroustumor influence gene expression and are associated with adverse patient outcome.
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The authors report an unusual intra- and extramedullary location for a solitary fibroustumor of the cervical spine.
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Ingleby describes a case of fibroustumor of the uterus terminating fatally, but not until three weeks after delivery.
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Solitary fibroustumor is a spindle cell tumor deriving from mesenchymal cells that arises most commonly in the pleura.
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Integrating TERT promoter mutational status with existing multivariable risk-prediction models might improve risk prediction in patients with solitary fibroustumor.
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The histological as well as the immunohistochemical examination revealed the mass to be a solitary fibroustumor of the pleura.
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Solitary fibroustumor (SFT) is rare mesenchymal neoplasm that has been originally and most often documented in the pleura.