When neuroglial tissue wanders: a unique case report of subpleural heterotopia in a triploid foetus and review of the literature

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F25%3AE0111932" target="_blank" >RIV/00843989:_____/25:E0111932 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/61988987:17110/25:A2603BVP RIV/00216208:11130/25:10503879 RIV/00064203:_____/25:10503879

Výsledek na webu

<a href="https://doi.org/10.3389/fmed.2025.1598144" target="_blank" >https://doi.org/10.3389/fmed.2025.1598144</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.3389/fmed.2025.1598144" target="_blank" >10.3389/fmed.2025.1598144</a>

Jazyk výsledku

angličtina

Název v původním jazyce

When neuroglial tissue wanders: a unique case report of subpleural heterotopia in a triploid foetus and review of the literature

Popis výsledku v původním jazyce

Heterotopic occurrence of neuroglial tissue is an exceedingly rare phenomenon with unclear pathogenesis, often presenting as lesions outside the central nervous system (CNS). We report a unique case of heterotopic neuroglial tissue identified in the thoracic cavity of a fetus aborted at 14 weeks due to a suspected Dandy-Walker malformation. The fetus exhibited neuroglial tissue growth subpleurally, alongside a suspected Dandy-Walker malformation and ventricular septal defect. While theories such as vascular embolisation, aspiration, and aberrant migration attempt to explain such occurrences, the exact etiology remains elusive. Our case suggests a potential association between triploidy and neuroglial heterotopia, supporting the aberrant migration and differentiation theory.

Název v anglickém jazyce

When neuroglial tissue wanders: a unique case report of subpleural heterotopia in a triploid foetus and review of the literature

Popis výsledku anglicky

Heterotopic occurrence of neuroglial tissue is an exceedingly rare phenomenon with unclear pathogenesis, often presenting as lesions outside the central nervous system (CNS). We report a unique case of heterotopic neuroglial tissue identified in the thoracic cavity of a fetus aborted at 14 weeks due to a suspected Dandy-Walker malformation. The fetus exhibited neuroglial tissue growth subpleurally, alongside a suspected Dandy-Walker malformation and ventricular septal defect. While theories such as vascular embolisation, aspiration, and aberrant migration attempt to explain such occurrences, the exact etiology remains elusive. Our case suggests a potential association between triploidy and neuroglial heterotopia, supporting the aberrant migration and differentiation theory.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

30109 - Pathology

Projekt

—

Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2025

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Frontiers in medicine

ISSN

2296-858X

e-ISSN

2296-858X

Svazek periodika

12

Číslo periodika v rámci svazku

article 1598144

Stát vydavatele periodika

CH - Švýcarská konfederace

Počet stran výsledku

9

Strana od-do

1-9

Kód UT WoS článku

001589064800001

EID výsledku v databázi Scopus

2-s2.0-105018724350