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Polymorphous low-grade neuroepithelial tumor of the young: Rare tumor and review of the literature.
Palejwala, Ali H; O'Neal, Christen M; Quinton, Michael R; Battiste, James D; Peterson, Jo Elle G; Dunn, Ian F.
Afiliação
  • Palejwala AH; Department of Neurosurgery, University of Oklahoma Health Sciences Center, Oklahoma City, Ok, USA.
  • O'Neal CM; Department of Neurosurgery, University of Oklahoma Health Sciences Center, Oklahoma City, Ok, USA.
  • Quinton MR; Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Ok, USA.
  • Battiste JD; Department of Neurosurgery, University of Oklahoma Health Sciences Center, Oklahoma City, Ok, USA.
  • Peterson JEG; Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Ok, USA.
  • Dunn IF; Department of Neurosurgery, University of Oklahoma Health Sciences Center, Oklahoma City, Ok, USA.
Rare Tumors ; 14: 20363613221083360, 2022.
Article em En | MEDLINE | ID: mdl-35371417
ABSTRACT
Polymorphous low-grade neuroepithelial tumor of the young (PLNTY) is a recently described low-grade neuroepithelial tumor with an infiltrative growth pattern and oligodendrocyte-like cells that are CD34 immunopositive. Correlating histology and results from molecular testing is critical to correctly diagnosing PLNTY, as its histologic appearance is similar to oligodendrogliomas and shares genetic abnormalities common to other low-grade epilepsy associated tumors (LEATs). In this case report, we describe a 31-year-old female with intractable epilepsy found to have a temporal mass and diagnosed with PLNTY after histopathologic and molecular testing. We describe the radiographic, histologic, and genetic features in relation to the epileptic and oncologic outcomes for this patient. Then, we compare these features and outcomes to other cases of PLNTY described in the literature.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Rare Tumors Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Rare Tumors Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos