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Wyświetlanie 1-2 z 2
Tytuł:
Epilepsy in paediatric patients with schizencephaly
Autorzy:
Kopyta, I.
Skrzypek, M.
Raczkiewicz, D.
Bojar, I.
Sarecka-Hujar, B.
Powiązania:
https://bibliotekanauki.pl/articles/2085589.pdf
Data publikacji:
2020
Wydawca:
Instytut Medycyny Wsi
Tematy:
schizencephaly
bilateral
unilateral
central nervous system malformation
epilepsy
developmental delay
Opis:
Introduction. Schizencephaly is one of the rare congenital defects of the central nervous system (CNS), known as neuronal migration disorders. The etiology of schizencecephaly is unequivocal. Established etiologies include in-utero infections (cytomegalovirus and herpes simplex virus, HSV type I), toxic abuse (cocaine, alcohol), as well as drug use (warfarin). Objectives. The aim of the study was to analyze the clinical presentation of schizencephaly with particular consideration of the course of epilepsy in paediatric patients. Materials and method. The study group consisted of 38 children with schizencephaly (20 of them had seizure) and was retrospectively assessed. Data were analyzed using SAS version 9.4. U Mann-Whitney and χ2 tests and logistic regression analysis were used in statistical analyses. Results. Epilepsy was the most frequent in bilateral type II schizencephaly (p=0.033). In logistic regression analysis, the presence of bilateral open schizencephaly significantly increased the risk of seizures (OR=11.67; 95%CI 2.44–55.83; p=0.002). Drug-resistant epilepsy was observed in 9 children (45% of the children with epilepsy). Prevalence of both epilepsy and drug-resistant epilepsy in schizencephaly did not significantly depend on gender, stage of development, type or localization of schizencephaly, and other coexisting CNS defects or clinical presentation of schizencephaly at follow-up in the study group of patients. Conclusions. The bilateral type of schizencephaly was identified as an independent risk factor for epilepsy in the analyzed children.
Źródło:
Annals of Agricultural and Environmental Medicine; 2020, 27, 2; 279-283
1232-1966
Pojawia się w:
Annals of Agricultural and Environmental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Hobnail hemangioma of the skin in a juvenile patient
Autorzy:
Ostrowska, A.
Golonka, A.
Bojar, P.
Pasnik, I.
Szumilo, J.
Powiązania:
https://bibliotekanauki.pl/articles/3353.pdf
Data publikacji:
2015
Wydawca:
Instytut Medycyny Wsi
Tematy:
hobnail hemangioma
skin
juvenile
patient
human disease
hobnail cell
vascular malformation
vascular neoplasm
Opis:
Hobnail hemangioma is a rare, benign, vascular lesion with peculiar but commonly misleading morphology, located mostly on the extremities or trunk, and affects young and middle-aged adults with a slightly male predominance. A new typical case in a 17-year-old girl is presented. A single, small, painless skin lesion appeared in an early childhood on the lateral part of the right thigh, and was linked with scratching a previous pigmented lesion. Microscopic examination of the completely removed lesion revealed typical morphology. Prominent endothelial cells were podoplanin-negative and CD34-positive. There was no recurrence after four years follow-up.
Źródło:
Journal of Pre-Clinical and Clinical Research; 2015, 09, 1
1898-2395
Pojawia się w:
Journal of Pre-Clinical and Clinical Research
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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