Obliterated cavum septi pellucidi: Clinical significance and role of fetal magnetic resonance

被引:1
|
作者
Fantasia, Ilaria [1 ,11 ]
Ciardo, Claudia [2 ]
Bracalente, Gabriella [3 ]
Filippi, Elisa [3 ]
Murru, Flora Maria [4 ]
Spezzacatene, Anita [4 ]
Bin, Maura [5 ]
Mendez Quintero, Olivia [6 ]
Montaguti, Elisa [7 ]
Lees, Christoph
Papanikolaou, Katherine [8 ]
Pilu, Gianluigi [7 ]
Prefumo, Federico [9 ]
Thilaganathan, Baskaran [6 ]
Stampalija, Tamara [1 ,10 ]
机构
[1] Unit Fetal Med, Inst Maternal & Child Hlth, IRCCS Burlo Garofolo, Trieste, Italy
[2] Osped Fracastoro, Dept Gynecol & Obstet, San Bonifacio, Italy
[3] Osped Ca Foncello Treviso, UOC Gynecol & Obstet, Treviso, Italy
[4] IRCCS Burlo Garofolo, Inst Maternal & Child Hlth, Radiol Serv, Trieste, Italy
[5] Inst Maternal & Child Hlth, Div Child Neurol & Psychiat, IRCCS Burlo Garofolo, Trieste, Italy
[6] St George Hosp, Fetal Med Unit, London, England
[7] Univ Bologna, IRCCS Azienda Osped, Obstet Unit, Bologna, Italy
[8] Queen Charlottes & Chelsea Hosp, Imperial Coll Healthcare NHS Trust, Ctr Fetal Care, London, England
[9] IRCCS Ist Giannina Gaslini, Obstet & Gynecol Unit, Genoa, Italy
[10] Univ Trieste, Dept Med Surg & Hlth Sci, Trieste, Italy
[11] IRCCS Burlo Garofolo, Inst Maternal & Child Hlth, Unit Fetal Med & Prenatal Diag, Via Istria 65-1, I-34137 Trieste, Italy
关键词
cavum septi pellucidi; fetal brain; fetal magnetic resonance; neurosonography; postnatal neurodevelopmental outcome; UPDATED SONOGRAPHIC EXAMINATION; CENTRAL-NERVOUS-SYSTEM; CORPUS-CALLOSUM; GUIDELINES; PERFORMANCE; AGENESIS; MIDLINE; BRAIN; ANTERIOR; SIGN;
D O I
10.1111/aogs.14575
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Introduction: The objective of this study was to describe a cohort of fetuses with an ultrasound prenatal diagnosis of obliterated cavum septi pellucidi (oCSP) with the aim to explore the rate of associated malformations, the progression during pregnancy and the role of fetal magnetic resonance imaging (MRI).Material and methods: This was a retrospective multicenter international study of fetuses diagnosed with oCSP in the second trimester with available fetal MRI and subsequent ultrasound and/or fetal MRI follow-up in the third trimester. Where available, postnatal data were collected to obtain information on neurodevelopment.Results: We identified 45 fetuses with oCSP at 20.5 weeks (interquartile range 20.1-21.1). oCSP was apparently isolated at ultrasound in 89% (40/45) and fetal MRI found additional findings in 5% (2/40) of cases, including polymicrogyria and microencephaly. In the remaining 38 fetuses, fetal MRI found a variable amount of fluid in CSP in 74% (28/38) and no fluid in 26% (10/38). Ultrasound follow-up at or after 30 weeks confirmed the diagnosis of oCSP in 32% (12/38) while fluid was visible in 68% (26/38). At follow-up MRI, performed in eight pregnancies, there were periventricular cysts and delayed sulcation with persistent oCSP in one case. Among the remaining cases with normal follow-up ultrasound and fetal MRI findings, the postnatal outcome was normal in 89% of cases (33/37) and abnormal in 11% (4/37): two with isolated speech delay, and two with neurodevelopmental delay secondary to postnatal diagnosis of Noonan syndrome at 5 years in one case and microcephaly with delayed cortical maturation at 5 months in the other.Conclusions: Apparently isolated oCSP at mid-pregnancy is a transient finding with the visualization of the fluid later in pregnancy in up to 70% of cases. At referral, associated defects can be found in around 11% of cases at ultrasound and 8% at fetal MRI indicating the need for a detailed evaluation by expert physicians when oCSP is suspected.
引用
收藏
页码:744 / 750
页数:7
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