Literature DB >> 30115677

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases.

P Codjia1, X Ayrignac2, F Mochel3, K Mouzat4, C Carra-Dalliere1, G Castelnovo5, E Ellie6, F Etcharry-Bouyx7, C Verny7, S Belliard8, D Hannequin9, C Marelli1, Y Nadjar10, I Le Ber10, I Dorboz11, S Samaan11, O Boespflug-Tanguy11, S Lumbroso4, P Labauge1.   

Abstract

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia is an autosomal dominant leukoencephalopathy related to CSF1R gene mutations. A growing number of clinicoradiologic phenotypes have been described. In this study, we analyzed brain imaging findings in 16 patients with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia to refine radiologic diagnostic clues. T2/FLAIR white matter hyperintensities were present in all patients with frontal or frontoparietal predilection, with asymmetric distribution in more than one-third. Brain atrophy and callosal involvement were almost constant, and corticospinal tract involvement was frequent. Moreover, deep white matter hyperintense dots on DWI and deep punctate calcifications on CT were often found. Conversely, deep gray matter nuclei, external capsules, and brain stem were rarely involved. Our series emphasized the great variability of MR imaging findings seen in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia. A complete imaging screening including DWI, T2*, and CT is mandatory to accurately assess patients with suspected inherited adult-onset leukoencephalopathy.
© 2018 by American Journal of Neuroradiology.

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Year:  2018        PMID: 30115677     DOI: 10.3174/ajnr.A5744

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  11 in total

Review 1.  Differential imaging of atypical demyelinating lesions of the central nervous system.

Authors:  Matteo Paoletti; Shaun Ivan Muzic; Francesca Marchetti; Lisa Maria Farina; Stefano Bastianello; Anna Pichiecchio
Journal:  Radiol Med       Date:  2021-01-24       Impact factor: 3.469

2.  Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of Microglia.

Authors:  Nynke Oosterhof; Irene J Chang; Ehsan Ghayoor Karimiani; Laura E Kuil; Dana M Jensen; Ray Daza; Erica Young; Lee Astle; Herma C van der Linde; Giridhar M Shivaram; Jeroen Demmers; Caitlin S Latimer; C Dirk Keene; Emily Loter; Reza Maroofian; Tjakko J van Ham; Robert F Hevner; James T Bennett
Journal:  Am J Hum Genet       Date:  2019-04-11       Impact factor: 11.025

3.  CSF1R Related Leukoencephalopathy - Rare Childhood Presentation of An Autosomal Dominant Microgliopathy!

Authors:  Neeharika Sriram; Hansashree Padmanabha; Sadanandavalli R Chandra; Rohan Mahale; Bevinahalli Nandeesh; Maya D Bhat; Rita Christopher; Manisha Gupta; Gautham A Udupi; Pooja Mailankody; Pavagada S Mathuranath
Journal:  Ann Indian Acad Neurol       Date:  2021-11-10       Impact factor: 1.714

4.  Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophy.

Authors:  Woutje M Berdowski; Herma C van der Linde; Marjolein Breur; Nynke Oosterhof; Shanice Beerepoot; Leslie Sanderson; Lieve I Wijnands; Patrick de Jong; Elisa Tsai-Meu-Chong; Walter de Valk; Moniek de Witte; Wilfred F J van IJcken; Jeroen Demmers; Marjo S van der Knaap; Marianna Bugiani; Nicole I Wolf; Tjakko J van Ham
Journal:  Acta Neuropathol       Date:  2022-06-17       Impact factor: 15.887

5.  Sustained, complete response to pexidartinib in a patient with CSF1R-mutated Erdheim-Chester disease.

Authors:  Jithma P Abeykoon; Terra L Lasho; Surendra Dasari; Karen L Rech; Wasantha K Ranatunga; Michelle K Manske; Alexander Tischer; Aishwarya Ravindran; Jason R Young; William Oliver Tobin; Eoin P Flanagan; Kevin E Nowakowski; Gordon J Ruan; Mithun V Shah; Nabila Nora Bennani; Robert Vassallo; Jay H Ryu; Matthew J Koster; Caroline J Davidge-Pitts; Mrinal M Patnaik; Xiaosheng Wu; Thomas E Witzig; Gaurav Goyal; Ronald S Go
Journal:  Am J Hematol       Date:  2022-01-03       Impact factor: 13.265

6.  Distinctive diffusion-weighted imaging features in late-onset genetic leukoencephalopathies.

Authors:  Laurens J L De Cocker; Mauricio Castillo
Journal:  Neuroradiology       Date:  2020-09-03       Impact factor: 2.804

7.  Deep White Matter Lesions with Persistent Diffusion Restriction on MRI as a Diagnostic Clue: Neuroimaging of a Turkish Family with Hereditary Diffuse Leukoencephalopathy with Spheroids and Literature Review.

Authors:  Halil Onder; Kader Karli Oguz; Figen Soylemezoglu; Kubilay Varli
Journal:  Ann Indian Acad Neurol       Date:  2020-06-10       Impact factor: 1.383

8.  Clinical and genetic characterization of adult-onset leukoencephalopathy caused by CSF1R mutations.

Authors:  Pei-Chien Tsai; Jong-Ling Fuh; Chih-Chao Yang; Anna Chang; Li-Ming Lien; Pei-Ning Wang; Kuan-Lin Lai; Yu-Shuen Tsai; Yi-Chung Lee; Yi-Chu Liao
Journal:  Ann Clin Transl Neurol       Date:  2021-10-15       Impact factor: 4.511

Review 9.  Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia: Review of Clinical Manifestations as Foundations for Therapeutic Development.

Authors:  Spyros Papapetropoulos; Angela Pontius; Elizabeth Finger; Virginija Karrenbauer; David S Lynch; Matthew Brennan; Samantha Zappia; Wolfgang Koehler; Ludger Schoels; Stefanie N Hayer; Takuya Konno; Takeshi Ikeuchi; Troy Lund; Jennifer Orthmann-Murphy; Florian Eichler; Zbigniew K Wszolek
Journal:  Front Neurol       Date:  2022-02-03       Impact factor: 4.003

Review 10.  Modeling CSF-1 receptor deficiency diseases - how close are we?

Authors:  Violeta Chitu; Şölen Gökhan; E Richard Stanley
Journal:  FEBS J       Date:  2021-07-05       Impact factor: 5.622

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