Morphological diversity in SDH-deficient renal carcinomas: a three-case exploration of variant features and dedifferentiation
Language English Country Germany Media print-electronic
Document type Case Reports, Journal Article
Grant support
5S340A202
Szent-Györgyi Albert Orvostudományi Kar, Szegedi Tudományegyetem
ÚNKP-23-2-SZTE-366
Magyarország Kormánya
PubMed
39562336
DOI
10.1007/s00428-024-03978-3
PII: 10.1007/s00428-024-03978-3
Knihovny.cz E-resources
- Keywords
- RCC, Renal cell carcinoma, SDHB, Succinate dehydrogenase,
- MeSH
- Cell Dedifferentiation MeSH
- Adult MeSH
- Fumarate Hydratase deficiency genetics MeSH
- Carcinoma, Renal Cell * genetics pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Biomarkers, Tumor genetics analysis MeSH
- Kidney Neoplasms * pathology genetics MeSH
- Aged MeSH
- Succinate Dehydrogenase * deficiency genetics MeSH
- Basic Helix-Loop-Helix Leucine Zipper Transcription Factors genetics MeSH
- Germ-Line Mutation MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Names of Substances
- Fumarate Hydratase MeSH
- Biomarkers, Tumor MeSH
- SDHB protein, human MeSH Browser
- Succinate Dehydrogenase * MeSH
- TFEB protein, human MeSH Browser
- Basic Helix-Loop-Helix Leucine Zipper Transcription Factors MeSH
Succinate dehydrogenase (SDH)-deficient renal cell carcinoma (RCC) is a rare subtype of renal neoplasm predominantly affecting younger individuals. It is characterized by germline mutations in SDHx genes, particularly type B. Histologically, SDH-deficient RCC features eosinophilic cytoplasmic cells forming solid nests or microcysts, sometimes entrapping normal tubules. We present three SDH-deficient RCC cases with overlapping morphological features with fumarate hydratase-deficient RCC and TFEB-rearranged RCC, an appearance that has not been previously described. All tumors lacked SDHB expression and harbored pathogenic SDHB mutations, with the germline nature confirmed in two cases. Metastasis developed in two patients. Our case set highlights the diagnostic challenges of molecularly defined renal tumors and expands the morphological spectrum of SDH-deficient RCC with unusual histological features. Clinically, these tumors appear to be aggressive.
Center for Urological Oncological Surgery National Institute of Oncology Budapest Hungary
Department of Molecular Genetics National Institute of Oncology Budapest Hungary
Department of Oncotherapy Albert Szent Györgyi Medical School University of Szeged Szeged Hungary
Department of Pathology Albert Szent Györgyi Medical School University of Szeged Szeged Hungary
Department of Pathology and Experimental Cancer Research Semmelweis University Budapest Hungary
Department of Pathology and Laboratory Medicine Albany Medical Center Albany NY USA
National Tumor Biology Laboratory National Institute of Oncology Budapest Hungary
See more in PubMed
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