Literature DB >> 24094860

Increasing and persistent DWI changes in a patient with hereditary diffuse leukoencephalopathy with spheroids.

Yuka Terasawa1, Yusuke Osaki, Toshitaka Kawarai, Tatsurou Sugimoto, Antonio Orlacchio, Takashi Abe, Yuishin Izumi, Ryuji Kaji.   

Abstract

We report a case with genetically confirmed hereditary diffuse leukoencephalopathy with spheroids with distinctive MRI features. A 52-year-old woman with a family history of juvenile dementia presented with an 18-month history of progressive cognitive decline. Longitudinal magnetic resonance imaging studies of the brain revealed increasing and persistent white matter hyperintensities on diffusion-weighted images. Linear high intensity signal along axonal fibers arisen from the cerebral cortex was also shown. Finding of subcortical calcifications was noted on brain CT scan. Sequence analysis of CSF1R showed a novel missense mutation c.2467C>T (p.Ala823Val). Persistent and increasing diffusion on magnetic resonance image, presumably reflecting intramyelinic oedema in regions of neurodegeneration, is a distinctive feature observed in this case. The presence of this unique finding can be a diagnostic clue in the early stage of the disease.
© 2013.

Entities:  

Keywords:  Colony stimulating factor 1 receptor (CSF1R); Diagnosis; Diffusion-weighted imaging (DWI); Hereditary Diffuse Leukoencephalopathy with Spheroids (HDLS); Magnetic resonance imaging (MRI); dJuvenile dementia

Mesh:

Substances:

Year:  2013        PMID: 24094860     DOI: 10.1016/j.jns.2013.08.027

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  14 in total

1.  Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis.

Authors:  Christina Sundal; Matt Baker; Rosa Rademakers; Oluf Andersen; Virginija Karrenbauer; Marte Gustavsen; Sahl Bedri; Anna Glaser; Kjell-Morten Myhr; Kristoffer Haugarvoll; Henrik Zetterberg; Hanne Harbo; Ingrid Kockum; Jan Hillert; Zbigniew Wszolek
Journal:  Eur J Neurol       Date:  2014-10-13       Impact factor: 6.089

Review 2.  CSF1R-related leukoencephalopathy: A major player in primary microgliopathies.

Authors:  Takuya Konno; Koji Kasanuki; Takeshi Ikeuchi; Dennis W Dickson; Zbigniew K Wszolek
Journal:  Neurology       Date:  2018-11-14       Impact factor: 9.910

3.  Imaging features in conventional MRI, spectroscopy and diffusion weighted images of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS).

Authors:  Benjamin Bender; Uwe Klose; Tobias Lindig; Saskia Biskup; Thomas Nägele; Ludger Schöls; Kathrin N Karle
Journal:  J Neurol       Date:  2014-09-20       Impact factor: 4.849

4.  Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia by a novel mutation of the CSF1R gene.

Authors:  Cong Ding; Li Zhao; Yu Zhan; Jiahao Li; Rujia Zhong; Qingwei Song; Chunbo Dong
Journal:  Neurol Sci       Date:  2022-08-16       Impact factor: 3.830

5.  Altered intrinsic brain activity in patients with CSF1R-related leukoencephalopathy.

Authors:  Jingying Wu; Yikang Cao; Mengting Li; Binyin Li; Xize Jia; Li Cao
Journal:  Brain Imaging Behav       Date:  2022-04-07       Impact factor: 3.224

Review 6.  Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): update on molecular genetics.

Authors:  Carmen Stabile; Ilaria Taglia; Carla Battisti; Silvia Bianchi; Antonio Federico
Journal:  Neurol Sci       Date:  2016-06-23       Impact factor: 3.307

7.  MR Spectroscopy in Patients with Hereditary Diffuse Leukoencephalopathy with Spheroids and Asymptomatic Carriers of Colony-stimulating Factor 1 Receptor Mutation.

Authors:  Takashi Abe; Toshitaka Kawarai; Koji Fujita; Wataru Sako; Yuka Terasawa; Tsuyoshi Matsuda; Waka Sakai; Ai Tsukamoto-Miyashiro; Naoko Matsui; Yuishin Izumi; Ryuji Kaji; Masafumi Harada
Journal:  Magn Reson Med Sci       Date:  2016-12-26       Impact factor: 2.471

Review 8.  Redefining the phenotype of ALSP and AARS2 mutation-related leukodystrophy.

Authors:  Rahul Lakshmanan; Matthew E Adams; David S Lynch; Justin A Kinsella; Rahul Phadke; Jonathan M Schott; Elaine Murphy; Jonathan D Rohrer; Jeremy Chataway; Henry Houlden; Nick C Fox; Indran Davagnanam
Journal:  Neurol Genet       Date:  2017-02-15

Review 9.  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

10.  Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation.

Authors:  T Konno; K Yoshida; T Mizuno; T Kawarai; M Tada; H Nozaki; S-I Ikeda; M Nishizawa; O Onodera; Z K Wszolek; T Ikeuchi
Journal:  Eur J Neurol       Date:  2016-09-29       Impact factor: 6.089

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