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Fibromyxoid aSoft Tissue Tumor With PLAG1 Fusion-The First Case in an Adult Patient
M. Strnadová, J. Balko, P. Brož, L. Wagenknecht, L. Krsková
Language English Country United States
Document type Case Reports, Journal Article
Grant support
Research Project of the Ministry of Health of Czech Republic No 00064203
PubMed
39576105
DOI
10.1002/gcc.70011
Knihovny.cz E-resources
- MeSH
- DNA-Binding Proteins * genetics MeSH
- Adult MeSH
- Fibroma genetics pathology MeSH
- Gene Fusion MeSH
- Oncogene Proteins, Fusion genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Soft Tissue Neoplasms * genetics pathology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
With the expanding possibilities of human genome research in recent years, the number of cases of soft tissue tumors that we are able to classify into the correct subgroups and to reveal their molecular profile is increasing. Among such tumors, we can also consider neoplasms that have a specific fusion of genes, in our case namely the pleomorphic adenoma gene 1 (PLAG1) and its partner. PLAG1 gene fusions were previously associated mainly with salivary gland pleomorphic adenomas, lipoblastomas, myoepithelial tumors, uterine epitheloid, myxoid leiomyosarcomas, and, recently, with PLAG1-rearranged fibromyxoid soft tissue tumors. To our knowledge, we report the first case of a soft tissue tumor with a PLAG1 fusion gene in an adult. In our case, we detected a new H3-3B::PLAG1 fusion in a soft tissue tumor, which originally appeared as nodular fasciitis.
References provided by Crossref.org
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