دورية أكاديمية
Feasibility and Added Value of Fetal DTI Tractography in the Evaluation of an Isolated Short Corpus Callosum: Preliminary Results.
العنوان: | Feasibility and Added Value of Fetal DTI Tractography in the Evaluation of an Isolated Short Corpus Callosum: Preliminary Results. |
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المؤلفون: | Millischer AE; From the Department of Paediatric Radiology (A.-E.M., D.G., P.S., V.D., N.B.), Assistance Publique-Hôpitaux de Paris, Hôpital Necker Enfants Malades, Université de Paris, Paris France aemillischer@gmail.com.; Institut Imagine (A.-E.M., D.G., P.S., N.B.-B., I.D., V.D., N.B.), Institut National de la Santé et de la Recherche Médicale U1163, Université de Paris, Paris, France.; LUMIERE Platform (A.-E.M., D.G., P.S., H.M., N.B., L.-J.S.), Paris, France.; IMPC Bachaumont (A.-E.M.), Paris, France., Grevent D; From the Department of Paediatric Radiology (A.-E.M., D.G., P.S., V.D., N.B.), Assistance Publique-Hôpitaux de Paris, Hôpital Necker Enfants Malades, Université de Paris, Paris France.; Institut Imagine (A.-E.M., D.G., P.S., N.B.-B., I.D., V.D., N.B.), Institut National de la Santé et de la Recherche Médicale U1163, Université de Paris, Paris, France.; LUMIERE Platform (A.-E.M., D.G., P.S., H.M., N.B., L.-J.S.), Paris, France., Sonigo P; From the Department of Paediatric Radiology (A.-E.M., D.G., P.S., V.D., N.B.), Assistance Publique-Hôpitaux de Paris, Hôpital Necker Enfants Malades, Université de Paris, Paris France.; Institut Imagine (A.-E.M., D.G., P.S., N.B.-B., I.D., V.D., N.B.), Institut National de la Santé et de la Recherche Médicale U1163, Université de Paris, Paris, France.; LUMIERE Platform (A.-E.M., D.G., P.S., H.M., N.B., L.-J.S.), Paris, France., Bahi-Buisson N; Institut Imagine (A.-E.M., D.G., P.S., N.B.-B., I.D., V.D., N.B.), Institut National de la Santé et de la Recherche Médicale U1163, Université de Paris, Paris, France.; Departments of Pediatric Neurology (N.B.-B., I.D.)., Desguerre I; Institut Imagine (A.-E.M., D.G., P.S., N.B.-B., I.D., V.D., N.B.), Institut National de la Santé et de la Recherche Médicale U1163, Université de Paris, Paris, France.; Departments of Pediatric Neurology (N.B.-B., I.D.)., Mahallati H; LUMIERE Platform (A.-E.M., D.G., P.S., H.M., N.B., L.-J.S.), Paris, France.; Department of Radiology (H.M.), University of Calgary, Calgary, Alberta, Canada., Bault JP; Departments of Gynecology and Obstetrics (J.-P.B., T.Q.)., Quibel T; Departments of Gynecology and Obstetrics (J.-P.B., T.Q.)., Couderc S; Pediatrics (S.C.), CHI, Poissy Saint-Germain, France., Moutard ML; Department of Pediatric Neurology (M.-L.M.), Trousseau Hospital, CHU, Trousseau, Paris., Julien E; Department of Gynecology-Obstetrics (E.J.), Hospital Le Mans, Le Mans, France., Dangouloff V; From the Department of Paediatric Radiology (A.-E.M., D.G., P.S., V.D., N.B.), Assistance Publique-Hôpitaux de Paris, Hôpital Necker Enfants Malades, Université de Paris, Paris France.; Institut Imagine (A.-E.M., D.G., P.S., N.B.-B., I.D., V.D., N.B.), Institut National de la Santé et de la Recherche Médicale U1163, Université de Paris, Paris, France., Bessieres B; Anatomical Pathology (B.B.)., Malan V; Genetics (V.M., T.A.), Necker Enfants Malades University Hospital, Université de Paris, Paris, France., Attie T; Genetics (V.M., T.A.), Necker Enfants Malades University Hospital, Université de Paris, Paris, France., Salomon LJ; Department of Gynecology-Obstetrics (L.-J.S.), Université de Paris, Paris, France.; LUMIERE Platform (A.-E.M., D.G., P.S., H.M., N.B., L.-J.S.), Paris, France., Boddaert N; From the Department of Paediatric Radiology (A.-E.M., D.G., P.S., V.D., N.B.), Assistance Publique-Hôpitaux de Paris, Hôpital Necker Enfants Malades, Université de Paris, Paris France.; Institut Imagine (A.-E.M., D.G., P.S., N.B.-B., I.D., V.D., N.B.), Institut National de la Santé et de la Recherche Médicale U1163, Université de Paris, Paris, France.; LUMIERE Platform (A.-E.M., D.G., P.S., H.M., N.B., L.-J.S.), Paris, France. |
المصدر: | AJNR. American journal of neuroradiology [AJNR Am J Neuroradiol] 2022 Jan; Vol. 43 (1), pp. 132-138. Date of Electronic Publication: 2021 Dec 23. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: American Society of Neuroradiology Country of Publication: United States NLM ID: 8003708 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1936-959X (Electronic) Linking ISSN: 01956108 NLM ISO Abbreviation: AJNR Am J Neuroradiol Subsets: MEDLINE |
أسماء مطبوعة: | Publication: Oak Brook, IL : American Society of Neuroradiology Original Publication: Baltimore, Williams & Wilkins. |
مواضيع طبية MeSH: | Agenesis of Corpus Callosum*/diagnostic imaging , Corpus Callosum*/diagnostic imaging, Feasibility Studies ; Fetus ; Humans ; Retrospective Studies |
مستخلص: | Background and Purpose: Prognosis of isolated short corpus callosum is challenging. Our aim was to assess whether fetal DTI tractography can distinguish callosal dysplasia from variants of normal callosal development in fetuses with an isolated short corpus callosum. Materials and Methods: This was a retrospective study of 37 cases referred for fetal DTI at 30.4 weeks (range, 25-34 weeks) because of an isolated short corpus callosum less than the 5th percentile by sonography at 26 weeks (range, 22-31 weeks). Tractography quality, the presence of Probst bundles, dysmorphic frontal horns, callosal length (internal cranial occipitofrontal dimension/length of the corpus callosum ratio), and callosal thickness were assessed. Cytogenetic data and neurodevelopmental follow-up were systematically reviewed. Results: Thirty-three of 37 fetal DTIs distinguished the 2 groups: those with Probst bundles (Probst bundles+) in 13/33 cases (40%) and without Probst bundles (Probst bundles-) in 20/33 cases (60%). Internal cranial occipitofrontal dimension/length of the corpus callosum was significantly higher in Probst bundles+ than in Probst bundles-, with a threshold value determined at 3.75 for a sensitivity of 92% (95% CI, 77%-100%) and specificity of 85% (95% CI, 63%-100%). Callosal lipomas (4/4) were all in the Probst bundles- group. More genetic anomalies were found in the Probst bundles+ than in Probst bundles- group (23% versus 10%, P = .08). Conclusions: Fetal DTI, combined with anatomic, cytogenetic, and clinical characteristics could suggest the possibility of classifying an isolated short corpus callosum as callosal dysplasia and a variant of normal callosal development. (© 2022 by American Journal of Neuroradiology.) |
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تواريخ الأحداث: | Date Created: 20211224 Date Completed: 20220310 Latest Revision: 20230102 |
رمز التحديث: | 20240628 |
مُعرف محوري في PubMed: | PMC8757544 |
DOI: | 10.3174/ajnr.A7383 |
PMID: | 34949593 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1936-959X |
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DOI: | 10.3174/ajnr.A7383 |