Clear cell stromal tumor of the lung with multinucleated giant cells: a report of a case with YAP1-TFE3 fusion
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu kazuistiky, časopisecké články
Grantová podpora
MH CZ DRO-VFN 64165
Ministerstvo Zdravotnictví Ceské Republiky
MH CZ DRO-VFN 64165
Ministerstvo Zdravotnictví Ceské Republiky
EF16_013/0001674
European Regional Development Fund
PubMed
36707859
PubMed Central
PMC9881279
DOI
10.1186/s13000-023-01304-0
PII: 10.1186/s13000-023-01304-0
Knihovny.cz E-zdroje
- Klíčová slova
- Clear cell (hemangioblastoma-like) stromal tumor, Lung, YAP1-TFE3 fusion,
- MeSH
- fúze genů MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádorové biomarkery genetika analýza MeSH
- nádory plic * genetika MeSH
- obrovské buňky chemie MeSH
- plíce MeSH
- transkripční faktory BHLH-Zip * genetika MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- Názvy látek
- nádorové biomarkery MeSH
- TFE3 protein, human MeSH Prohlížeč
- transkripční faktory BHLH-Zip * MeSH
BACKGROUND: Clear cell (hemangioblastoma-like) stromal tumor of the lung (CCSTL) is a rare pulmonary neoplasm. Recently, 9 cases of CCSTL harboring the YAP1-TFE3 gene fusion have been described, and it has been suggested that this aberration could be a characteristic feature of this tumor. CASE PRESENTATION: We here report another case of CCSTL in a 57-year-old male, which presented as a solitary lung nodule 45 mm in the greatest dimension. Microscopically, the tumor consisted of epithelioid to spindled cells with mild-to-moderate nuclear atypia, finely granular or vesicular chromatin, and small nucleoli. Nuclear indentations were a common finding. There were up to 3 mitoses per 10 HPF. The cytoplasm was slightly eosinophilic or clear. Scattered non-tumor large multinucleated cells were present. Immunohistochemically, the tumor cells showed diffuse positivity for TFE3, CD10, vimentin, and IFITM1. Other markers examined were negative, and the expression of lineage-specific markers was not found. NGS analysis revealed a fusion transcript of the YAP1 and TFE3 genes, and a pathogenic variant of the MUTYH gene. CONCLUSION: Our finding supports the recent data suggesting that CCSTL represents a distinct entity characterized by the recurrent YAP1-TFE3 fusion.
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