Abstract
Dermatofibrosarcoma protuberans (DFSP) is a rare malignant soft tissue tumor in children. DFSP is characterized by a specific fusion of the platelet-derived growth factor β (PDGFβ) with the collagen type 1α1 (COL1α1) gene which renders these tumors responsive to targeted therapy with tyrosine kinase inhibitors, such as imatinib mesylate, as is reported in adults. In the current report, we describe the first small pediatric DFSP series, in which response to imatinib mesylate contributed to successful treatment outcome.
| Original language | English |
|---|---|
| Pages (from-to) | 369-373 |
| Number of pages | 5 |
| Journal | Pediatric Blood and Cancer |
| Volume | 55 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Aug 2010 |
| Externally published | Yes |
Keywords
- Children
- Dermatofibrosarcoma protuberans
- Imatinib
- Treatment
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