RESUMO
OBJECTIVE: To establish the prevalence of COL4A1 and COL4A2 gene mutations in fetuses presenting with a phenotype suggestive of cerebral injury. METHODS: This was a single-center retrospective analysis of all cases of fetal cerebral anomalies suggestive of COL4A1 or COL4A2 gene mutation over the period 2009-2018. Inclusion criteria were: (1) severe and/or multifocal hemorrhagic cerebral lesions; (2) multifocal ischemic-hemorrhagic cerebral lesions. These anomalies could be of different ages and associated with schizencephaly or porencephaly. Between fetuses with and those without a mutation, we compared gestational age at the time of diagnosis, parity and fetal gender. RESULTS: Among the 956 cases of cerebral anomaly diagnosed in our center during the 10-year study period, 18 fetuses were identified for inclusion. A pathogenic COL4A1 gene mutation was found in five of these cases, among which four were de-novo mutations. A variant of unknown significance was found in four fetuses: in the COL4A1 gene in one case and in the COL4A2 gene in three cases. No COL4A1 or COL4A2 mutation was found in the remaining nine fetuses. The median (interquartile range) gestational age at diagnosis was significantly lower in cases with a mutation (24 (22-26) weeks) than in cases without a mutation (32 (29.5-34.5) weeks) (P = 0.03). CONCLUSIONS: A phenotype suggestive of cerebral injury was found in 18 of the 956 (1.9%) cases in our population, in 28% of which there was an associated COL4A1 or COL4A2 mutation. COL4A1 and COL4A2 gene mutations should be sought systematically in cases of severe and/or multifocal hemorrhagic or ischemic-hemorrhagic cerebral lesions, with or without schizencephaly or porencephaly. © 2020 International Society of Ultrasound in Obstetrics and Gynecology.
Assuntos
Hemorragia Cerebral/embriologia , Hemorragia Cerebral/genética , Colágeno Tipo IV/genética , Malformações do Desenvolvimento Cortical/embriologia , Malformações do Desenvolvimento Cortical/genética , Adulto , Hemorragia Cerebral/diagnóstico , Feminino , Idade Gestacional , Humanos , Malformações do Desenvolvimento Cortical/diagnóstico , Mutação , Fenótipo , Porencefalia/diagnóstico , Porencefalia/embriologia , Porencefalia/genética , Gravidez , Resultado da Gravidez/genética , Diagnóstico Pré-Natal/métodos , Prevalência , Estudos Retrospectivos , Esquizencefalia/diagnóstico , Esquizencefalia/embriologia , Esquizencefalia/genéticaRESUMO
OBJECTIVE: The purpose of this study is to define the role of foetal magnetic resonance imaging (MRI) in evaluating cerebral ischaemic-haemorrhagic lesions and the extension of parenchymal injuries. STUDY DESIGN: From September 2006 to September 2010, 271 foetal MRI have been performed on cases referred to us for ultrasound suspect of brain abnormalities or cytomegalovirus infection and Toxoplasma serum conversion. Foetal MRI was performed with a 1.5-T magnet system without mother sedation. RESULTS: Foetal MRI detected ischaemic-haemorrhagic lesions in 14 of 271 foetuses, consisting of 5% incidence. MRI confirmed the diagnosis in three of 14 cases with ultrasonography (US) suspect of ischaemic-haemorrhagic lesions associated with ventriculomegaly. In one of 14 cases with US findings of cerebellar haemorrhage, MRI confirmed the diagnosis and provided additional information regarding the parenchymal ischaemic injury. In eight of 14 cases with US suspect of ventriculomegaly (3), corpus callosum agenesis (2), hypoplasia of cerebellar vermis (1), holoprosencephaly (1) and spina bifida (1), MRI detected ischaemic and haemorrhagic lesions unidentified at US examination. In two of 14 foetuses with US suspect of intracerebral space-occupying lesion, MRI modified the diagnosis to extra-axial haematoma associated with dural sinus malformation. Results were compared with post-mortem findings or afterbirth imaging follow-up. CONCLUSIONS: Foetal MRI is an additional imaging modality in the diagnosis of cerebral ischemic-haemorrhagic lesions, and it is useful in providing further information on the extension of the parenchymal injury and associated abnormalities, thus improving delivery management.
Assuntos
Isquemia Encefálica/embriologia , Hemorragia Cerebral/embriologia , Doenças Fetais/diagnóstico , Imageamento por Ressonância Magnética , Diagnóstico Pré-Natal/métodos , Anormalidades Múltiplas , Adulto , Agenesia do Corpo Caloso/diagnóstico , Isquemia Encefálica/diagnóstico , Isquemia Encefálica/patologia , Doenças Cerebelares/diagnóstico , Cerebelo/anormalidades , Hemorragia Cerebral/diagnóstico , Hemorragia Cerebral/patologia , Infecções por Citomegalovirus/diagnóstico , Anormalidades do Olho/diagnóstico , Feminino , Doenças Fetais/patologia , Idade Gestacional , Holoprosencefalia/diagnóstico , Humanos , Doenças Renais Císticas/diagnóstico , Gravidez , Retina/anormalidades , Disrafismo Espinal/diagnósticoRESUMO
The purpose of this study was to validate the recommendation of the American Academy of Neurology and the Child Neurology Society that screening cranial ultrasonography be performed routinely on all infants of less than 30 weeks gestation at 7 to 14 days of age and again between 36 and 40 weeks postmenstrual age, and, by using this practice parameter, to determine the number of babies with a clinically significant abnormal screening cranial ultrasound (US) who would otherwise have been missed. A retrospective study of 486 infants of 30 to 33 weeks gestation born January 1, 1999 to June 30, 2004 was done. All had screening cranial ultrasounds. Grade III and/or grade IV intraventricular hemorrhage (IVH) occurred in 4 (0.8%) infants of 30 to 31 weeks gestation. Infants with significant IVH had either risk factors for brain injury or symptoms that would eventually warrant US during their hospitalization. Seven (1.4%) infants had periventricular leukomalacia (PVL). All infants with a final diagnosis of PVL had pre- and/or perinatal risk factors associated with PVL. There was a significant trend toward fewer abnormal cranial ultrasounds from 30 to 33 weeks gestation (p=0.04). Our study supports the recommendation by the American Academy of Neurology and the Child Neurology Society that screening US can be limited but suggests that the gestational age cut off should be 30 weeks or less.
Assuntos
Hemorragia Cerebral/diagnóstico por imagem , Ventrículos Cerebrais/diagnóstico por imagem , Testes Diagnósticos de Rotina/estatística & dados numéricos , Doenças do Prematuro/diagnóstico por imagem , Recém-Nascido Prematuro , Triagem Neonatal/estatística & dados numéricos , Ultrassonografia Pré-Natal/estatística & dados numéricos , Hemorragia Cerebral/embriologia , Hemorragia Cerebral/epidemiologia , Ventrículos Cerebrais/embriologia , Parto Obstétrico/estatística & dados numéricos , Feminino , Idade Gestacional , Humanos , Recém-Nascido , Doenças do Prematuro/embriologia , Doenças do Prematuro/epidemiologia , Leucomalácia Periventricular/diagnóstico por imagem , Leucomalácia Periventricular/embriologia , Leucomalácia Periventricular/epidemiologia , Prontuários Médicos , Guias de Prática Clínica como Assunto , Valor Preditivo dos Testes , Gravidez , Estudos Retrospectivos , Sociedades Médicas , Texas/epidemiologia , Procedimentos Desnecessários/estatística & dados numéricosRESUMO
PURPOSE: White matter damage of immaturity may affect visual, motor and cognitive functions. This multiple-case study presents standardized perimetry results in six teenagers and young adults born prematurely with visual dysfunction due to white matter damage of immaturity of pre- or perinatal origin. METHODS: Six subjects, aged 13-25 years, born at a gestational age of 28-34 weeks, with white matter damage of immaturity documented by MRI, and optic disc appearances documented by fundus photography, were examined with manual and computerized quantitative perimetry. RESULTS: All subjects had subnormal visual field (VF) function, although the depth and extension of the VF defects differed between subjects. The inferior VF function was more deviant than the superior in all cases. The concordance between the VF defects detected with the different techniques was good, although the static computerized techniques revealed slightly more abnormality. CONCLUSION: White matter damage of immaturity may affect the VF. The lower VF is often more affected than the upper. The abnormalities can be demonstrated by both manual and computerized perimetry.
Assuntos
Hemorragia Cerebral/complicações , Recém-Nascido Prematuro , Leucomalácia Periventricular/complicações , Transtornos da Visão/etiologia , Campos Visuais , Adolescente , Adulto , Hemorragia Cerebral/diagnóstico , Hemorragia Cerebral/embriologia , Feminino , Idade Gestacional , Humanos , Recém-Nascido , Leucomalácia Periventricular/diagnóstico , Leucomalácia Periventricular/embriologia , Imageamento por Ressonância Magnética/métodos , Masculino , Disco Óptico/patologia , Doenças do Nervo Óptico/diagnóstico , Doenças do Nervo Óptico/embriologia , Doenças do Nervo Óptico/etiologia , Transtornos da Visão/diagnóstico , Transtornos da Visão/embriologia , Testes de Campo Visual/métodosRESUMO
BACKGROUND AND PURPOSE: Little is known about the different patterns of fetal cerebral ischemic lesions at MR imaging. Our purpose was to evaluate the contribution of MR imaging in the evaluation of such lesions by correlating the results with ultrasonography (US) and neurofetopathologic (NFP) findings. METHODS: We examined 28 fetuses (mean, 28 weeks' gestation) with cerebral ischemic lesions on NFP examination. MR findings were correlated with US and NFP results with regard to the depiction of gyration and parenchymal abnormalities. RESULTS: MR imaging added to US findings in 24 cases by revealing lesions (gyration abnormalities, parenchymal lesions). These results were either overlooked during US (n = 16) or more extensive than expected with US (n = 8). MR findings were always confirmed by NFP. NFP yielded additional findings for 14 lesions that were overlooked during MR imaging (n = 4) or that were more extensive than expected with MR imaging (n = 10). T1-, T2-, and T2*-weighted MR patterns of different lesions (cavitations, gliosis, softening of the white matter, laminar necrosis, calcified leukomalacia, old hemorrhage) were identified. CONCLUSION: MR imaging is a valuable tool in the evaluation of fetal brain ischemia. The results of this study emphasize the role of the different sequences (T1-, T2-, T2*-weighted) required to detect fetal cerebral ischemic lesions. MR imaging is more accurate in the detection of small focal lesions than in the evaluation of diffuse white matter abnormalities.
Assuntos
Isquemia Encefálica/embriologia , Encéfalo/embriologia , Imageamento por Ressonância Magnética , Diagnóstico Pré-Natal , Encéfalo/patologia , Dano Encefálico Crônico/embriologia , Dano Encefálico Crônico/patologia , Isquemia Encefálica/diagnóstico , Isquemia Encefálica/patologia , Hemorragia Cerebral/diagnóstico , Hemorragia Cerebral/embriologia , Hemorragia Cerebral/patologia , Feminino , Gliose/diagnóstico , Gliose/embriologia , Gliose/patologia , Humanos , Recém-Nascido , Leucomalácia Periventricular/diagnóstico , Leucomalácia Periventricular/embriologia , Leucomalácia Periventricular/patologia , Masculino , Necrose , Gravidez , Prognóstico , Sensibilidade e Especificidade , Estatística como Assunto , Ultrassonografia Pré-NatalRESUMO
AIMS: To evaluate the relation between optic disc morphology and timing of periventricular white matter damage, defined as either periventricular leucomalacia (PVL) or periventricular haemorrhage (PVH), as estimated by neuroradiology. METHODS: 35 children with periventricular white matter damage who had had neuroradiology performed and ocular fundus photographs taken had their photographs analysed by digital image analysis and compared with a control group of 100 healthy full term children. Timing of brain lesion was estimated by analysis of the brain lesion pattern on neuroradiological examinations (magnetic resonance imaging or computed tomography). RESULTS: Four of 35 children had a small optic disc area; these four children had a brain lesion estimated to have occurred before 28 weeks of gestation. Nine of 11 children with a large cup area had a PVL/PVH estimated to have occurred after 28 weeks of gestation. The children with PVL/PVH had a significantly larger cup area (median 0.75 mm(2)) than the control group (median 0.33 mm(2)) (p = 0.001) and a significantly smaller neuroretinal rim area (median 1.58 mm(2)) than the controls (median 2.07 mm(2)) (p = 0.001). CONCLUSION: In a child with PVL/PVH and abnormal optic disc morphology, the possibilities of timing of the lesion should be considered.
Assuntos
Hemorragia Cerebral/patologia , Leucomalácia Periventricular/patologia , Disco Óptico/patologia , Estudos de Casos e Controles , Hemorragia Cerebral/embriologia , Feminino , Fundo de Olho , Idade Gestacional , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Leucomalácia Periventricular/embriologia , Disco Óptico/embriologia , Gravidez , Estatísticas não Paramétricas , Acuidade VisualRESUMO
Subependymal germinal matrix hemorrhage with intraventricular hemorrhage(SEIVH) is a common complication associated with delivery in preterm neonates but has rarely been observed in the fetus. We report a fetus with SEIVH, hydrocephalus and periventricular leukomalacia(PVL). Although this fetus had uneventful prenatal periods, transabdominal ultrasound examination(US) at 33 weeks of pregnancy revealed SEIVH and hydrocephalus, and MRI at 36 weeks did associated PVL. While no events reported that could explain the onset of SEIVH, PVL was considered to be the results of anoxic events associated with SEIVH. In addition to US, information provided by fetal MRI, especially T 2-weighted image, permits a better understanding of the pathophysiology of fetal SEIVH with PVL.
Assuntos
Hemorragia Cerebral/diagnóstico , Hemorragia Cerebral/embriologia , Ventrículos Cerebrais/embriologia , Leucomalácia Periventricular/diagnóstico , Leucomalácia Periventricular/embriologia , Adulto , Hemorragia Cerebral/complicações , Feminino , Idade Gestacional , Humanos , Recém-Nascido , Leucomalácia Periventricular/etiologia , Imageamento por Ressonância Magnética , Gravidez , Diagnóstico Pré-NatalRESUMO
Immunization against the human platelet antigen (HPA)-1 alloantigen is the most common cause of severe fetal and neonatal thrombocytopenia. Fetal therapy has substantial risks and its indications need better definition. Of 24,417 consecutive pregnant women, 618 (2.5%) were HPA-1a negative of whom 385 entered an observational study. All were HLA-DRB3*0101 genotyped and screened for anti-HPA-1a. Their partners and neonates were HPA-1 genotyped and the latter were assessed by cord blood platelet counts and cerebral ultrasound scans. Anti-HPA-1a was detected in 46 of 387 pregnancies (12.0%; 95% CI 8.7%-15.2%). All but one were HLA-DRB3*0101 positive (odds ratio 140; 95% CI 19-1035; P< .00001). One baby died in utero, and of 26 HPA-1a-positive babies born to women with persistent antenatal antibodies, 9 were severely thrombocytopenic (8 with a count <10 x 10(9)/L, 1 with a large porencephalic cyst), 10 were mildly thrombocytopenic, whereas 7 had normal platelet counts. Severe thrombocytopenia was significantly associated with a third trimester anti-HPA-1a titer >/= 1:32 (P = . 004), but was not observed in babies of women with either transient or postnatal-only antibodies. HPA-1a alloimmunization complicates 1 in 350 unselected pregnancies, resulting in severe thrombocytopenia in 1:1,200. HPA-1a and HLA-DRB3*0101 typing combined with anti-HPA-1a titration allows selection of the majority of pregnancies at risk of severe thrombocytopenia.
Assuntos
Antígenos de Plaquetas Humanas/imunologia , Imunidade Materno-Adquirida , Imunização , Diagnóstico Pré-Natal , Trombocitopenia/genética , Aborto Espontâneo/etiologia , Adulto , Antígenos de Plaquetas Humanas/genética , Hemorragia Cerebral/congênito , Hemorragia Cerebral/diagnóstico por imagem , Hemorragia Cerebral/embriologia , Hemorragia Cerebral/etiologia , Inglaterra/epidemiologia , Feminino , Sangue Fetal/citologia , Morte Fetal/etiologia , Doenças Fetais/diagnóstico por imagem , Doenças Fetais/etiologia , Antígenos HLA-DR/genética , Cadeias HLA-DRB3 , Humanos , Hidrocefalia/etiologia , Recém-Nascido , Integrina beta3 , Isoanticorpos/sangue , Paridade , Contagem de Plaquetas , Valor Preditivo dos Testes , Gravidez , Resultado da Gravidez , Terceiro Trimestre da Gravidez , Estudos Prospectivos , Fatores de Risco , Trombocitopenia/congênito , Trombocitopenia/imunologia , Trombocitopenia/prevenção & controle , Ultrassonografia Pré-NatalRESUMO
Connatal periventricular pseudocysts are important sequelae of different noxious insults in the developing brain. Accurate diagnosis of those pathologic entities during early life has therefore become of direct concern to the clinician. Our experience with 12 infants of connatal periventricular pseudocysts provides the basis of this study. They belonged to different pathological entities: focal paraventricular pseudocysts (5 cases), subependymal pseudocyst (3 cases), connatal viral infection (3 cases), and chromosomal abnormality (1 case). When present at birth, they suggest an intrauterine pathology. It has only been with the advent of real-time cranial ultrasound that periventricular pseudocystic lesions can be detected in neonates following an abnormal pregnancy. Some obstetric complications during the second trimester can cause paraventricular or subependymal pseudocyst in the foetus. Neurotrophic viral infection and chromosomal abnormalities have also been implicated in the production of cystic lesions in this region. These lesions are not a terminal event in infants but may be a condition of major clinical importance for further neurological development.