Literature DB >> 25093633

Constrained spherical deconvolution-based tractography to depict and characterize a case of "hyperplastic fornix dorsalis".

Valeria Elisa Contarino1, Sara Bulgheroni2, Mario Savoiardo3, Silvia Annunziata2, Domenico Aquino3, Daria Riva2, Alessandra Erbetta3.   

Abstract

The authors report the relevance of Constrained Spherical Deconvolution (CSD)-based tractography in demonstrating and quantitatively assessing a complex midline structure malformation in a 9-year-old girl with moderate intellectual disability and thickening of corpus callosum (CC) body discovered through conventional MRI (cMRI). Color-encoded fractional anisotropy (FA) maps clearly demonstrated what the cMRI showed as a thicknening of CC: a green, longitudinal bundle running dorsally to the body of CC. A more complex midline maldevelopmental disorder was suspected. CSD-based tractography was performed to virtually dissect the anomalous supracallosal longitudinal bundle (SLB), CC, fornix, anterior commissure (AC) and cingula. In addition, DTI-derived metrics were calculated for each virtually dissected fiber tract. The tractography study evidenced projections of the anomalous SLB in left forceps minor and to parietal regions, and projections of the fornix in right forceps minor. CC virtual dissection showed no gross abnormality, and cingula appeared slightly less extended than normal. The considerable thinning of AC hampered its virtual dissection. DTI-derived metrics suggested alterations in fornix microstructure, attributable to higher fiber density. In investigating white matter, cMRI may not be sufficient in addressing and assessing possible anomalies, while advanced CSD-based tractography and DTI-derived metrics may prove helpful in depicting and characterizing white matter anomalies in developmental disorders.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Constrained spherical deconvolution-based tractography; Diffusion Tensor Imaging; Intellectual disability; Midline malformations; Supracallosal bundle

Mesh:

Year:  2014        PMID: 25093633     DOI: 10.1016/j.mri.2014.07.007

Source DB:  PubMed          Journal:  Magn Reson Imaging        ISSN: 0730-725X            Impact factor:   2.546


  2 in total

1.  Long-distance aberrant heterotopic connectivity in a mouse strain with a high incidence of callosal anomalies.

Authors:  Diego Szczupak; Cirong Liu; Cecil C C Yen; Sang-Ho Choi; Fernanda Meireles; Caroline Victorino; Linda Richards; Roberto Lent; Afonso C Silva; Fernanda Tovar-Moll
Journal:  Neuroimage       Date:  2020-04-23       Impact factor: 6.556

2.  Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice.

Authors:  Milka Pringsheim; Diana Mitter; Simone Schröder; Rita Warthemann; Kim Plümacher; Gerhard Kluger; Martina Baethmann; Thomas Bast; Sarah Braun; Hans-Martin Büttel; Elizabeth Conover; Carolina Courage; Alexandre N Datta; Angelika Eger; Theresa A Grebe; Annette Hasse-Wittmer; Marion Heruth; Karen Höft; Angela M Kaindl; Stephanie Karch; Torsten Kautzky; Georg C Korenke; Bernd Kruse; Richard E Lutz; Heymut Omran; Steffi Patzer; Heike Philippi; Keri Ramsey; Tina Rating; Angelika Rieß; Mareike Schimmel; Rachel Westman; Frank-Martin Zech; Birgit Zirn; Pauline A Ulmke; Godwin Sokpor; Tran Tuoc; Andreas Leha; Martin Staudt; Knut Brockmann
Journal:  Ann Clin Transl Neurol       Date:  2019-03-03       Impact factor: 4.511

  2 in total

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