Dedifferentiated solitary fibrous tumor of thoracic cavityopen access
- Authors
- Yang, J.W.; Song, D.H.; Jang, I.S.; Ko, G.H.
- Issue Date
- 2014
- Publisher
- Seoul National University
- Citation
- Korean Journal of Pathology, v.48, no.3, pp 250 - 253
- Pages
- 4
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- Korean Journal of Pathology
- Volume
- 48
- Number
- 3
- Start Page
- 250
- End Page
- 253
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/20133
- DOI
- 10.4132/KoreanJPathol.2014.48.3.250
- ISSN
- 1738-1843
2092-8920
- Abstract
- Solitary fibrous tumor (SFT) is a mesenchymal tumor characterized by fibroblast-like tumor cells, thick collagen bands, a hemangiopericytoma-like branching vascular pattern and CD34 expression of tumor cells.1 Although some cases show malignant behavior, most of the cases are benign and have histologically bland-looking tumor cells. Rarely, highly pleomorphic sarcoma arises within a primary or recurrent SFT having typical histologic features. This is a phenomenon similar to that seen in dedifferentiated liposarcoma. Dedifferentiated SFT (DSFT) is rare, with less than 30 cases reported worldwide,2-6 and it has not been previously reported in Korea. Here, we present a case of DSFT. ? 2014 The Korean Society of Pathologists.
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