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1000 Titel
  • Molecular characterization of CNS paragangliomas identifies cauda equina paragangliomas as a distinct tumor entity
1000 Autor/in
  1. Schweizer, Leonille |
  2. Thierfelder, Felix |
  3. Thomas, Christian |
  4. Soschinski, Patrick |
  5. Suwala, Abigail |
  6. Stichel, Damian |
  7. Wefers, Annika K. |
  8. Wessels, Lars |
  9. Misch, Martin |
  10. Kim, Hee-yeong |
  11. Jödicke, Ruben |
  12. Teichmann, Daniel |
  13. Kaul, David |
  14. Kahn, Johannes |
  15. Bockmayr, Michael |
  16. Hasselblatt, Martin |
  17. Younsi, Alexander |
  18. Unterberg, Andreas |
  19. Knie, Bettina |
  20. Walter, Jan |
  21. Al Safatli, Diaa |
  22. May, Sven-Axel |
  23. Jödicke, Andreas |
  24. Ntoulias, Georgios |
  25. Moskopp, Dag |
  26. Vajkoczy, Peter |
  27. Heppner, Frank L. |
  28. Capper, David |
  29. Hartmann, Wolfgang |
  30. Hartmann, Christian |
  31. von Deimling, Andreas |
  32. Reuss, David E. |
  33. Schöler, Anne |
  34. Koch, Arend |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-09-14
1000 Erschienen in
1000 Quellenangabe
  • 140(6):893-906
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00401-020-02218-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666289/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Paragangliomas/pheochromocytomas are rare neuroendocrine tumors that arise from the adrenal gland or ganglia at various sites throughout the body. They display a remarkable diversity of driver alterations and are associated with germline mutations in up to 40% of the cases. Comprehensive molecular profiling of abdomino-thoracic paragangliomas revealed four molecularly defined and clinically relevant subtypes. Paragangliomas of the cauda equina region are considered to belong to one of the defined molecular subtypes, but a systematic molecular analysis has not yet been performed. In this study, we analyzed genome-wide DNA methylation profiles of 57 cauda equina paragangliomas and show that these tumors are epigenetically distinct from non-spinal paragangliomas and other tumors. In contrast to paragangliomas of other sites, chromosomal imbalances are widely lacking in cauda equina paragangliomas. Furthermore, RNA and DNA exome sequencing revealed that frequent genetic alterations found in non-spinal paragangliomas-including the prognostically relevant SDH mutations-are absent in cauda equina paragangliomas. Histologically, cauda equina paragangliomas show frequently gangliocytic differentiation and strong immunoreactivity to pan-cytokeratin and cytokeratin 18, which is not common in paragangliomas of other sites. None of our cases had a familial paraganglioma syndrome. Tumors rarely recurred (9%) or presented with multiple lesions within the spinal compartment (7%), but did not metastasize outside the CNS. In summary, we show that cauda equina paragangliomas represent a distinct, sporadic tumor entity defined by a unique clinical and morpho-molecular profile.
1000 Sacherschließung
lokal SDHB
lokal Head and neck
lokal Original Paper
lokal Paraganglioma
lokal DNA methylation
lokal GATA3
lokal Cauda equina
1000 Liste der Beteiligten
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