J 2021

Polymorphous low-grade neuroepithelial tumor of the young

HENDRYCH, Michal, Jan HEMZA, Jitka KOČVAROVÁ, Eva PEŠLOVÁ, Daniela SOCHŮRKOVÁ et. al.

Basic information

Original name

Polymorphous low-grade neuroepithelial tumor of the young

Name in Czech

Polymorfní low-grade neuroepiteliální tumor mladých

Authors

HENDRYCH, Michal (203 Czech Republic, guarantor, belonging to the institution), Jan HEMZA (203 Czech Republic, belonging to the institution), Jitka KOČVAROVÁ (203 Czech Republic, belonging to the institution), Eva PEŠLOVÁ (203 Czech Republic, belonging to the institution), Daniela SOCHŮRKOVÁ (203 Czech Republic, belonging to the institution), Irena DOLEŽALOVÁ (203 Czech Republic, belonging to the institution), Eva BRICHTOVÁ (203 Czech Republic, belonging to the institution), Martin PAIL (203 Czech Republic, belonging to the institution), Milan BRÁZDIL (203 Czech Republic, belonging to the institution), Radim JANČÁLEK (203 Czech Republic, belonging to the institution), Jiří VANÍČEK (203 Czech Republic, belonging to the institution) and Markéta HERMANOVÁ (203 Czech Republic, belonging to the institution)

Edition

Česká a slovenská neurologie a neurochirurgie, Praha, Česká lékařská společnost J. E. Purkyně, 2021, 1210-7859

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30109 Pathology

Country of publisher

Czech Republic

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

Impact factor

Impact factor: 0.411

RIV identification code

RIV/00216224:14110/21:00123826

Organization unit

Faculty of Medicine

UT WoS

000747009900011

Keywords in English

Polymorphous low-grade neuroepithelial tumor of the young

Tags

International impact, Reviewed
Změněno: 17/5/2022 12:49, Mgr. Tereza Miškechová

Abstract

V originále

Hereby we would like to present a case report of a 27-year-old male patient with drug- -resistant structural epilepsy based on the diagnosis of the polymorphous low‑grade neuroepithelial tumor of the young (PLNTY), first reported by Huse et al in 2017 [1]. PLNTY is a sporadic epileptogenic tumor characterized by an oligodendroglial-like component, diffuse CD34 expression, and alteration of the mitogen-activated protein (MAP) kinase signaling pathway. It shares multiple characteristics with other diffuse low-grade gliomas, especially with oligodendroglioma; nevertheless, its distinction is crucial because of the favorable prognosis of PLNTY.

Links

MUNI/A/1645/2020, interní kód MU
Name: Možnosti využití ADC ke zpřesnění detekce tumorózní infiltrace u high-grade gliálních tumorů (Acronym: Využití ADC ke zpřesnění detekce infiltrace u HGG)
Investor: Masaryk University