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Titolo:
Congenital subependymal pseudocysts: Own data and meta-analysis of the literature
Autore:
Makhoul, IR; Zmora, O; Tamir, A; Shahar, E; Sujov, P;
Indirizzi:
Rambam Med Ctr, Dept Neonatol, IL-31096 Haifa, Israel Rambam Med Ctr Haifa Israel IL-31096 pt Neonatol, IL-31096 Haifa, Israel Rambam Med Ctr, Dept Community Med & Epidemiol, IL-31096 Haifa, Israel Rambam Med Ctr Haifa Israel IL-31096 & Epidemiol, IL-31096 Haifa, Israel Rambam Med Ctr, Dept Pediat Neurol, IL-31096 Haifa, Israel Rambam Med CtrHaifa Israel IL-31096 diat Neurol, IL-31096 Haifa, Israel Technion Israel Inst Technol, Rappaport Fac Med, IL-31096 Haifa, Israel Technion Israel Inst Technol Haifa Israel IL-31096 L-31096 Haifa, Israel
Titolo Testata:
ISRAEL MEDICAL ASSOCIATION JOURNAL
fascicolo: 3, volume: 3, anno: 2001,
pagine: 178 - 183
SICI:
1565-1088(200103)3:3<178:CSPODA>2.0.ZU;2-H
Fonte:
ISI
Lingua:
ENG
Soggetto:
PERIVENTRICULAR PSEUDOCYSTS; FOLLOW-UP; CYSTS; DIAGNOSIS; LIFE; SONOGRAPHY; ULTRASOUND; LESIONS; NEONATE;
Keywords:
pseudocyst; subependymal cyst; ultrasound; germinal matrix; newborn; ventricle;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Citazioni:
39
Recensione:
Indirizzi per estratti:
Indirizzo: Makhoul, IR Rambam Med Ctr, Dept Neonatol, IL-31096 Haifa, Israel Rambam Med Ctr Haifa Israel IL-31096 IL-31096 Haifa, Israel
Citazione:
I.R. Makhoul et al., "Congenital subependymal pseudocysts: Own data and meta-analysis of the literature", ISR MED ASS, 3(3), 2001, pp. 178-183

Abstract

Background: Congenital subependymal pseudocysts are incidental findings that are round in 0.5-5.2% of neonates during postmortem examination or head ultrasonography. In our institution we detected 10 neonates with CSEPC,Objective: To investigate associated etiological factors, morphologic characteristics and outcome of CSEPC,Methods: We performed a mete-analysis of the literature on CSEPC (1967-98), including our 10 cases. Results: A total of 256 cases of CSEPC were analyzed. Ultrasound diagnosed77.6% of CSEPC; 48.8% were bilateral and 53.4% were located in the caudothalamic groove or head of caudate nucleus. Altogether, 93.5% resolved during1-12 months of ultrasonographic follow-up. Compared to the general neonatal population, the following features were more prevalent in the CSEPC population: prematurity, maternal Vaginal bleeding, preeclamptic toxemia, intrauterine growth restriction, asphyxia, fetal cytomegalovirus and rubella infections, congenital malformations, chromosomal aberrations, infant mortality, and neurodevelopmental handicap. The risk for neurodevelopmental handicapwas significantly higher when CSEPC were associated with fetal infections,IUGR, malformations and chromosomal aberrations, or persistence of CSEPC during follow-up, CSEPC infants without any of these four conditions had a low risk for neurodevelopmental handicap,Conclusions: CSEPC are morphologic features of various underlying conditions encountered in the fetus, Association of CSEPC with IUGR, fetal infections, malformations and chromosomal aberrations or persistence of CSEPC indicates a higher risk for future neurodevelopmental handicaps, probably because of the deleterious effects on the fetal brain that are inherent in these conditions. A favorable outcome is expected in the absence of these risk factors.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/07/20 alle ore 20:21:55