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Clear cell renal cell carcinoma with focal psammomatous calcifications: a rare occurrence mimicking translocation carcinoma
AR. Sangoi, KI. Al-Obaidy, L. Cheng, CS. Kao, E. Chan, S. Sadasivan, AM. Levin, I. Alvarado-Cabrero, LP. Kunju, R. Mehra, R. Mannan, X. Wang, J. Dhillon, M. Tretiakova, SC. Smith, O. Hes, SR. Williamson
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
PubMed
36564980
DOI
10.1111/his.14854
Knihovny.cz E-zdroje
- MeSH
- chromozomální aberace MeSH
- kalcinóza * MeSH
- karcinom z renálních buněk * patologie MeSH
- lidé MeSH
- nádorové biomarkery genetika MeSH
- nádory ledvin * patologie MeSH
- transkripční faktory BHLH-Zip genetika MeSH
- translokace genetická MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
AIMS: Renal cell carcinoma (RCC) with clear cells and psammoma-like calcifications would often raise suspicion for MITF family translocation RCC. However, we have rarely encountered tumours consistent with clear cell RCC that contain focal psammomatous calcifications. METHODS AND RESULTS: We identified clear cell RCCs with psammomatous calcifications from multiple institutions and performed immunohistochemistry and fluorescence and RNA in-situ hybridisation (FISH and RNA ISH). Twenty-one tumours were identified: 12 men, nine women, aged 45-83 years. Tumour size was 2.3-14.0 cm (median = 6.75 cm). Nucleolar grade was 3 (n = 14), 2 (n = 4) or 4 (n = 3). In addition to clear cell pattern, morphology included eosinophilic (n = 12), syncytial giant cell (n = 4), rhabdoid (n = 2), branched glandular (n = 1), early spindle cell (n = 1) and poorly differentiated components (n = 1). Labelling for CA9 was usually 80-100% of the tumour cells (n = 17 of 21), but was sometimes decreased in areas of eosinophilic cells (n = 4). All (19 of 19) were positive for CD10. Most (19 of 20) were positive for AMACR (variable staining = 20-100%). Staining was negative for keratin 7, although four showed rare positive cells (four of 20). Results were negative for cathepsin K (none of 19), melan A (none of 17), HMB45 (none of 17), TFE3 (none of 5), TRIM63 RNA ISH (none of 13), and TFE3 (none of 19) and TFEB rearrangements (none of 12). Seven of 19 (37%) showed chromosome 3p deletion. One (one of 19) showed trisomy 7 and 17 without papillary features. CONCLUSIONS: Psammomatous calcifications in RCC with a clear cell pattern suggests a diagnosis of MITF family translocation RCC; however, psammomatous calcifications can rarely be found in true clear cell RCC.
Biopticka Laboratory Plzen Czech Republic
Brown University Warren Albert Medical School Providence RI USA
Cleveland Clinic Cleveland OH USA
El Camino Hospital Mountain View CA USA
H Lee Moffitt Cancer Center and Research Institute Tampa FL USA
Henry Ford Health System Detroit MI USA
Mexican Oncology Hospital SXXI IMSS Mexico City Mexico
Stanford Medicine Stanford University Stanford CA USA
University of California San Francisco CA USA
University of Michigan Ann Arbor MI USA
Citace poskytuje Crossref.org
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