Expanding the clinicopathological spectrum of succinate dehydrogenase-deficient renal cell carcinoma with a focus on variant morphologies: a study of 62 new tumors in 59 patients
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
34949766
DOI
10.1038/s41379-021-00998-1
PII: S0893-3952(22)00058-8
Knihovny.cz E-resources
- MeSH
- Adult MeSH
- Hyperplasia MeSH
- Immunohistochemistry MeSH
- Carcinoma, Renal Cell * genetics pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Kidney Neoplasms * genetics pathology MeSH
- Necrosis MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Succinate Dehydrogenase genetics MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Succinate Dehydrogenase MeSH
Most succinate dehydrogenase (SDH)-deficient renal cell carcinomas (RCCs) demonstrate stereotypical morphology characterized by bland eosinophilic cells with frequent intracytoplasmic inclusions. However, variant morphologic features have been increasingly recognized. We therefore sought to investigate the incidence and characteristics of SDH-deficient RCC with variant morphologies. We studied a multi-institutional cohort of 62 new SDH-deficient RCCs from 59 patients. The median age at presentation was 39 years (range 19-80), with a slight male predominance (M:F = 1.6:1). A relevant family history was reported in 9 patients (15%). Multifocal or bilateral tumors were identified radiologically in 5 patients (8%). Typical morphology was present at least focally in 59 tumors (95%). Variant morphologies were seen in 13 (21%) and included high-grade nuclear features and various combinations of papillary, solid, and tubular architecture. Necrosis was present in 13 tumors, 7 of which showed variant morphology. All 62 tumors demonstrated loss of SDHB expression by immunohistochemistry. None showed loss of SDHA expression. Germline SDH mutations were reported in all 18 patients for whom the results of testing were known. Among patients for whom follow-up data was available, metastatic disease was reported in 9 cases, 8 of whom had necrosis and/or variant morphology in their primary tumor. Three patients died of disease. In conclusion, variant morphologies and high-grade nuclear features occur in a subset of SDH-deficient RCCs and are associated with more aggressive behavior. We therefore recommend grading all SDH-deficient RCCs and emphasize the need for a low threshold for performing SDHB immunohistochemistry in any difficult to classify renal tumor, particularly if occurring at a younger age.
Anatomical Pathology Douglass Hanly Moir Pathology Sonic Healthcare Macquarie Park NSW Australia
Aquesta Pathology Toowong QLD Australia
Brigham and Women's Hospital and Harvard Medical School Boston MA USA
Cancer Diagnosis and Pathology Group Kolling Institute of Medical Research St Leonards NSW Australia
Complejo Hospitalario de Navarra Navarra Spain
Discipline of Pathology Macquarie Medical School Macquarie University Macquarie Park NSW Australia
Fundació Puigvert Universitat Autonoma de Barcelona Barcelona Spain
Houston Methodist Hospital Houston TX USA
Institut de Pathologie Centre de Biologie Pathologie CHRU Lille France
Lab Plus Auckland DHB Auckland New Zealand
Leeds Teaching Hospital Leeds UK
Mater Health Brisbane QLD Australia
McGill University Montreal Canada
McMaster University Hamilton Ontario Canada
Medical Faculty and University Hospital Plzen Charles University Prague Plzen Czech Republic
NHLS Bloemfontein Area Bloemfontein South Africa
NHS Lothian Edinburgh Scotland UK
Northwestern University Chicago IL USA
Oncocentro Foundation Sao Paulo Brazil
PathCare Mediclinic Bloemfontein Hospital Bloemfontein South Africa
Peking University Shenzhen Hospital Shenzhen China
Queen Elizabeth Hospital Kowloon Hong Kong SAR China
Robert J Tomsich Pathology and Laboratory Medicine Institute Cleveland Clinic Cleveland Ohio OH USA
St Teresa's Hospital Kowloon Hong Kong SAR China
Stanford University Medical Center Stanford CA USA
Sunshine Coast University Hospital Pathology Queensland Birtinya QLD Australia
Sydney Medical School The University of Sydney Sydney Australia
The University of Texas MD Anderson Cancer Center Houston TX USA
TissuPath Pathology Melbourne VIC Australia
Tufts Medical Center Boston MA USA
University of California San Francisco San Francisco CA USA
University of Michigan Ann Arbor MI USA
University of Pennsylvania Philadelphia PA USA
See more in PubMed
Gill, A. J. Succinate dehydrogenase (SDH) deficient neoplasia. Histopathology 72, 106–116 (2018). PubMed DOI
Gill, A. J. Succinate dehydrogenase (SDH) and mitochondrial driven neoplasia. Pathology 44, 285–292 (2012). PubMed DOI
Gill, A. J. et al. Immunohistochemistry for SDHB triages genetic testing of SDHB, SDHC and SDHD in paraganglioma-phaeochromocytoma syndromes. Hum. Pathol. 41, 805–814 (2010). PubMed DOI
Gill, A. J. et al. Succinate dehydrogenase deficiency is rare in pituitary adenomas. Am. J. Surg. Pathol. 38, 560–566 (2014). PubMed DOI
Turchini, J. & Gill, A. J. Morphological clues to succinate dehydrogenase (SDH) deficiency in pheochromocytomas and paragangliomas. Am. J. Surg. Pathol. 44, 422–424 (2020). PubMed DOI
Williamson, S. R. et al. Report from the International Society of Urological Pathology (ISUP) Consultation Conference on Molecular Pathology of Urogenital Cancers: III: Molecular Pathology of Kidney Cancer. Am. J. Surg. Pathol. 44, e47–e65 (2020). PubMed DOI
Gill, A. J. et al. Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients. Am. J. Surg. Pathol. 38, 1588–1602 (2014). PubMed DOI
Gill, A. J. et al. Renal tumors associated with germline SDHB mutation show distinctive morphology. Am. J. Surg. Pathol. 35, 1578–1585 (2011). PubMed DOI
Gill, A. J. et al. Renal tumors and hereditary pheochromocytoma-paraganglioma syndrome. N Engl. J. Med. 364, 885–886 (2011). PubMed DOI
Gill, A. J. et al. Immunohistochemistry for SDHB divides gastrointestinal stromal tumors (GISTs) into 2 distinct types. Am. J. Surg. Pathol. 34, 636–644 (2010). PubMed DOI
Dwight, T. et al. Familial SDHA mutation associated with pituitary adenoma and pheochromocytoma/paraganglioma. J. Clin. Endocrinol. Metab. 98, E1103–E1108 (2013). PubMed DOI
Williamson, S. R. et al. Succinate dehydrogenase-deficient renal cell carcinoma: detailed characterization of 11 tumors defining a unique subtype of renal cell carcinoma. Mod. Pathol. 28, 80–94 (2015). PubMed DOI
Trpkov, K. et al. Novel, emerging and provisional renal entities: The Genitourinary Pathology Society (GUPS) Update on Renal Neoplasia. Mod. Pathol. 34, 1167–1184 (2021). PubMed DOI
Trpkov, K. et al. New developments in existing WHO entities and evolving molecular concepts: The Genitourinary Pathology Society (GUPS) Update on Renal Neoplasia. Mod. Pathol. 34, 1392–142 (2021). PubMed DOI
Gill, A. J. et al. Germline SDHC mutation presenting as recurrent SDH deficient GIST and renal carcinoma. Pathology 45, 689–691 (2013). PubMed DOI
Smith, S. C. et al. A distinctive, low-grade oncocytic fumarate hydratase-deficient renal cell carcinoma, morphologically reminiscent of succinate dehydrogenase-deficient renal cell carcinoma. Histopathology 71, 42–52 (2017). PubMed DOI
Korpershoek, E. et al. SDHA immunohistochemistry detects germline SDHA gene mutations in apparently sporadic paragangliomas and pheochromocytomas. J. Clin. Endocrinol. Metab. 96, E1472–E1476 (2011). PubMed DOI
Yakirevich, E. et al. A novel SDHA-deficient renal cell carcinoma revealed by comprehensive genomic profiling. Am. J. Surg. Pathol. 39, 858–863 (2015). PubMed DOI
Ozluk, Y. et al. Renal carcinoma associated with a novel succinate dehydrogenase A mutation: a case report and review of literature of a rare subtype of renal carcinoma. Hum. Pathol. 46, 1951–1955 (2015). PubMed DOI
Jiang, Q. et al. A novel germline mutation in SDHA identified in a rare case of gastrointestinal stromal tumor complicated with renal cell carcinoma. Int. J. Clin. Exp. Pathol. 8, 12188–12197 (2015). PubMed PMC
McEvoy, C. R. et al. SDH-deficient renal cell carcinoma associated with biallelic mutation in succinate dehydrogenase A: comprehensive genetic profiling and its relation to therapy response. NPJ Precis. Oncol. 2, 9 (2018). PubMed DOI
Moch, H., Humphrey, P. A., Ulbright, T. M. & Reuter, V. E. WHO Classification of Tumours of the Urinary System and Male Genital Organs 4th edn. (IARC Press, 2017).
Li, Y. et al. Re-evaluation of 33 ‘unclassified’ eosinophilic renal cell carcinomas in young patients. Histopathology 72, 588–600 (2018). PubMed DOI
Ricketts, C. et al. Succinate dehydrogenase kidney cancer: an aggressive example of the warburg effect in cancer. J. Urol. 188, 2063–2071 (2012). PubMed DOI
Kennedy, J. M. et al. Clinical and morphologic review of 60 hereditary renal tumors from 30 hereditary renal cell carcinoma syndrome patients: lessons from a contemporary single institution series. Med. Oncol. 36, 74 (2019). PubMed DOI
Casey, R. T. et al. Clinical and molecular features of renal and pheochromocytoma/paraganglioma tumor association syndrome (RAPTAS): case series and literature review. J. Clin. Endocrinol. Metab. 102, 4013–4022 (2017). PubMed DOI
Dwight, T. et al. Loss of SDHA expression identifies SDHA mutations in succinate dehydrogenase-deficient gastrointestinal stromal tumors. Am. J. Surg. Pathol. 37, 226–233 (2013). PubMed DOI
Samaratunga, H. et al. Granular necrosis: a distinctive form of cell death in malignant tumours. Pathology 52, 507–514 (2020). PubMed DOI
Trpkov, K. et al. Low-grade oncocytic tumour of kidney (CD117-negative, cytokeratin 7-positive): a distinct entity? Histopathology 75, 174–184 (2019). PubMed DOI
Al-Obaidy, K. I. et al. EWSR1-PATZ1 fusion renal cell carcinoma: a recurrent gene fusion characterizing thyroid-like follicular renal cell carcinoma. Mod. Pathol. 34, 1921–1934 (2021). PubMed DOI
Kuroda, N. et al. ALK rearranged renal cell carcinoma (ALK-RCC): a multi-institutional study of twelve cases with identification of novel partner genes CLIP1, KIF5B and KIAA1217. Mod. Pathol. 33, 2564–2579 (2020). PubMed DOI
Benn, D. E. et al. Bayesian approach to determining penetrance of pathogenic SDH variants. J. Med. Genet. 55, 729–734 (2018). PubMed DOI