Long-term epilepsy associated tumor

From Libre Pathology
Revision as of 14:57, 6 November 2020 by Jensflorian (talk | contribs) (+ refs)
Jump to navigation Jump to search

Long-term epilepsy associated tumors, abbreviated LEAT is an umbrella term for rare tumor entities in patients that do not match current WHO diagnostic criteria.

General


Examples

  • Papillary glioneuronal tumor [1]
  • Angiocentric glioma [2]
  • Isomorphic diffuse glioma [3]
  • Multinodular and vacuolating neuronal tumor of the cerebrum [4]
  • Polymorphous low grade tumor of the young [5]


Criteria

  • Seizures <18 years.
  • Temporal lobe location.
  • Mostly benign appearance (as in WHO grade I).

See also

References

  1. "Papillary glioneuronal tumour: a review of the literature with two illustrative cases". Br J Neurosurg 27 (3): 401–4. June 2013. doi:10.3109/02688697.2012.741735. PMID 23173837.
  2. "Rare glial tumors". Handb Clin Neurol 134: 399–415. 2016. doi:10.1016/B978-0-12-802997-8.00024-4. PMID 26948368.
  3. "Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course". Acta Neuropathol 139 (1): 193–209. January 2020. doi:10.1007/s00401-019-02078-w. PMC 7477753. PMID 31563982. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477753/.
  4. "Multinodular and vacuolating neuronal tumor of the cerebrum: Two cases and review of the literature". Clin Neurol Neurosurg 197: 106149. October 2020. doi:10.1016/j.clineuro.2020.106149. PMID 32979644.
  5. "Polymorphous low-grade neuroepithelial tumor of the young (PLNTY): an epileptogenic neoplasm with oligodendroglioma-like components, aberrant CD34 expression, and genetic alterations involving the MAP kinase pathway". Acta Neuropathol 133 (3): 417–429. March 2017. doi:10.1007/s00401-016-1639-9. PMC 5325850. PMID 27812792. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325850/.