Eosinophilic vacuolated tumor (EVT) of kidney demonstrates sporadic TSC/MTOR mutations: next-generation sequencing multi-institutional study of 19 cases
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie, práce podpořená grantem
PubMed
34521993
DOI
10.1038/s41379-021-00923-6
PII: S0893-3952(22)00311-8
Knihovny.cz E-zdroje
- MeSH
- dospělí MeSH
- karcinom z renálních buněk * patologie MeSH
- ledviny patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- lokální recidiva nádoru MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mutace MeSH
- nádorové biomarkery genetika metabolismus MeSH
- nádory ledvin * patologie MeSH
- senioři MeSH
- TOR serin-threoninkinasy genetika MeSH
- variabilita počtu kopií segmentů DNA MeSH
- vysoce účinné nukleotidové sekvenování MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- MTOR protein, human MeSH Prohlížeč
- nádorové biomarkery MeSH
- TOR serin-threoninkinasy MeSH
A distinct renal tumor has recently been described as "high-grade oncocytic renal tumor" and "sporadic renal cell carcinoma with eosinophilic and vacuolated cytoplasm". The Genitourinary Pathology Society (GUPS) consensus proposed a unifying name "eosinophilic vacuolated tumor" (EVT) for this emerging entity. In this multi-institutional study, we evaluated 19 EVTs, particularly their molecular features and mutation profile, using next-generation sequencing. All cases were sporadic and none of the patients had a tuberous sclerosis complex. There were 8 men and 11 women, with a mean age of 47 years (median 50; range 15-72 years). Average tumor size was 4.3 cm (median 3.8 cm; range 1.5-11.5 cm). All patients with available follow-up data (18/19) were alive and without evidence of disease recurrence or progression during the follow-up, ranging from 12 to 198 months (mean 56.3, median 41.5 months). The tumors were well circumscribed, but lacked a well-formed capsule, had nested to solid growth, focal tubular architecture, and showed ubiquitous, large intracytoplasmic vacuoles, round to oval nuclei, and prominent nucleoli. Immunohistochemically, cathepsin K, CD117, CD10, and antimitochondrial antigen were expressed in all cases. Other positive stains included: PAX8, AE1/AE3 and CK18. CK7 was typically restricted only to rare scattered cells. Vimentin, HMB45, melan-A, and TFE3 were negative in all cases. All tumors showed retained SDHB. All cases (19/19) showed non-overlapping mutations of the mTOR pathway genes: TSC1 (4), TSC2 (7), and MTOR (8); one case with MTOR mutation showed a coexistent RICTOR missense mutation. Low mutational rates were found in all samples (ranged from 0 to 6 mutations/Mbp). Microsatellite instability and copy number variations were not found in any of the 17 analyzable cases. EVT represents an emerging renal entity that shows a characteristic and readily identifiable morphology, consistent immunohistochemical profile, indolent behavior, and mutations in either TSC1, TSC2, or MTOR genes.
Caris Life Sciences Phoenix AZ USA
Department of Pathology Alfa Medical Bratislava Slovakia
Department of Pathology British Columbia University Vancouver Canada
Department of Pathology Colentina Clinical Hospital Bucharest Romania
Department of Pathology Cruces University Hospital Biocruces Bizkaia Institute Barakaldo Spain
Department of Pathology El Camino Hospital Mountain View CA USA
Department of Pathology Heath Science Centre St John's NL Canada
Department of Pathology Institute Nacional de Cancerologia Mexico City Mexico
Department of Pathology McGill University Montreál QC Canada
Department of Pathology Oklahoma University School of Medicine Oklahoma USA
Department of Pathology School of Medicine University of Alabama Birmingham AL USA
Department of Pathology Stradin´s University Riga Latvia
Department of Pathology Tufts Medical Center Boston MA USA
Department of Pathology Universitätsklinikum Hamburg Eppendorf Hamburg Germany
Department of Pathology University Hospital Nitra Nitra Slovakia
Department of Pathology University Hospital Ostrava Ostrava Czech Republic
Department of Pathology University of Erlangen Erlangen Germany
Department of Pathology University of Szeged Szeged Hungary
Department of Pathology University of Toronto Toronto ON Canada
Department of Pathology University of Vienna Vienna Austria
Department of Pathology University of Washington School of Medicine Seattle WA USA
Department of Urology University of Erlangen Erlangen Germany
Onco Team Diagnostic Bucharest Romania
Robert J Tomsich Pathology and Laboratory Medicine Institute Cleveland Clinic Cleveland OH USA
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