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Malignant Solitary Fibrous Tumor
- Source :
- Applied Immunohistochemistry & Molecular Morphology. 17:451-457
- Publication Year :
- 2009
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2009.
-
Abstract
- Malignant solitary fibrous tumor (MSFT) is a rare neoplasm. Three cases of MSFT with unusual features, including 1 pleural and 2 extrapleural, are reported. A 64-year-old woman with a large right thoracic MSFT and episodes of severe hypoglycemia experienced resolution of her hypoglycemia immediately after resection of the MSFT. A 27-year-old woman with primary retroperitoneal MSFT had pulmonary metastases 10 months after resection of the primary tumor. A 54-year-old man with an intracranial solitary fibrous tumor suffered from multiple pulmonary metastases and local recurrence 21 and 28 months after resection of the primary tumor, respectively. All 3 cases of solitary fibrous tumor displayed malignant features. The tumor cells in each case were positive for CD34 and Bcl-2, but negative for cytokeratin, smooth muscle actin, S-100, and c-kit. In addition, the tumor cells in the case with concomitant hypoglycemia were strongly positive for insulin-like growth factor-II. The histopathologic diagnostic criteria for MSFT, the differential diagnosis with other spindle cell tumors, and the mechanism of MSFT-derived hypoglycemia via insulin-like growth factor-II are discussed.
- Subjects :
- Adult
Male
Pathology
medicine.medical_specialty
Solitary fibrous tumor
Histology
business.industry
CD34
Malignant Solitary Fibrous Tumor
Fibroma
Middle Aged
Hypoglycemia
medicine.disease
Immunohistochemistry
Primary tumor
Pathology and Forensic Medicine
Medical Laboratory Technology
Cytokeratin
medicine
Humans
Neoplasm
Female
Differential diagnosis
Tomography, X-Ray Computed
business
Subjects
Details
- ISSN :
- 15412016
- Volume :
- 17
- Database :
- OpenAIRE
- Journal :
- Applied Immunohistochemistry & Molecular Morphology
- Accession number :
- edsair.doi.dedup.....805b0adb22c22a27d013b9f7c719b29f
- Full Text :
- https://doi.org/10.1097/pai.0b013e318198f23e