Literature DB >> 34167956

Neuroimaging Findings in Retinal Vasculopathy with Cerebral Leukoencephalopathy and Systemic Manifestations.

E S Hoogeveen1, N Pelzer2, I de Boer2, M A van Buchem1, G M Terwindt2, M C Kruit3.   

Abstract

Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations is caused by TREX1 mutations. High-quality systematic follow-up neuroimaging findings have not been described in presymptomatic and symptomatic mutation carriers. We present MR imaging findings of 29 TREX1 mutation carriers (20-65 years of age) and follow-up of 17 mutation carriers (30-65 years of age). Mutation carriers younger than 40 years of age showed a notable number of punctate white matter lesions, but scan findings were generally unremarkable. From 40 years of age onward, supratentorial lesions developed with long-term contrast enhancement (median, 24 months) and diffusion restriction (median, 8 months). In these lesions, central susceptibility artifacts developed, at least partly corresponding to calcifications on available CT scans. Some lesions (n = 2) additionally showed surrounding edema and mass effect (pseudotumors). Cerebellar punctate enhancing lesions developed mainly in individuals older than 50 years of age. These typical neuroimaging findings should aid neuroradiologic recognition of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations, which may enable early treatment of manifestations of the disease.
© 2021 by American Journal of Neuroradiology.

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Year:  2021        PMID: 34167956      PMCID: PMC8423035          DOI: 10.3174/ajnr.A7194

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   4.966


  18 in total

1.  Evolution of a tumor-like lesion in cerebroretinal vasculopathy and TREX1 mutation.

Authors:  F J Mateen; K Krecke; B R Younge; A L Ford; A Shaikh; P H Kothari; J P Atkinson
Journal:  Neurology       Date:  2010-09-28       Impact factor: 9.910

2.  Hereditary retinal vasculopathy with cerebral white matter lesions.

Authors:  D H Gutmann; K H Fischbeck; R C Sergott
Journal:  Am J Med Genet       Date:  1989-10

3.  Magnetic Resonance Imaging Characteristics of Retinal Vasculopathy with Cerebral Leukoencephalopathy and Systemic Manifestations.

Authors:  D M Hedderich; N Lummel; M Deschauer; T Kümpfel; E Schuh; M Patzig; C Zimmer; T Huber
Journal:  Clin Neuroradiol       Date:  2019-01-09       Impact factor: 3.649

4.  Retinal Vasculopathy With Cerebral Leukodystrophy: Clinicopathologic Features of an Autopsied Patient With a Heterozygous TREX 1 Mutation.

Authors:  Rie Saito; Hiroaki Nozaki; Taisuke Kato; Yasuko Toyoshima; Hajime Tanaka; Yutaka Tsubata; Tetsuo Morioka; Yoh Horikawa; Kiyomitsu Oyanagi; Takashi Morita; Osamu Onodera; Akiyoshi Kakita
Journal:  J Neuropathol Exp Neurol       Date:  2019-02-01       Impact factor: 3.685

5.  Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS).

Authors:  J Jen; A H Cohen; Q Yue; J T Stout; H V Vinters; S Nelson; R W Baloh
Journal:  Neurology       Date:  1997-11       Impact factor: 9.910

6.  Cerebroretinal vasculopathy mimicking a brain tumor: a case of a rare hereditary syndrome.

Authors:  S Weil; G Reifenberger; C Dudel; T A Yousry; S Schriever; S Noachtar
Journal:  Neurology       Date:  1999-08-11       Impact factor: 9.910

7.  Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon.

Authors:  G M Terwindt; J Haan; R A Ophoff; S M Groenen; C W Storimans; J B Lanser; R A Roos; E M Bleeker-Wagemakers; R R Frants; M D Ferrari
Journal:  Brain       Date:  1998-02       Impact factor: 13.501

Review 8.  Neuropathology and genetics of cerebroretinal vasculopathies.

Authors:  Grant R Kolar; Parul H Kothari; Negar Khanlou; Joanna C Jen; Robert E Schmidt; Harry V Vinters
Journal:  Brain Pathol       Date:  2014-09       Impact factor: 6.508

9.  Phenotypic Variability in a Mexican Mestizo Family with Retinal Vasculopathy with Cerebral Leukodystrophy and TREX1 Mutation p.V235Gfs*6.

Authors:  Nancy Monroy-Jaramillo; Aurelio Cerón; Elizabeth León; Verónica Rivas; Adriana Ochoa-Morales; María Georgina Arteaga-Alcaraz; Fausto Carlos Nocedal-Rustrian; Cecilia Gallegos; María Elisa Alonso-Vilatela; Teresa Corona; José Flores
Journal:  Rev Invest Clin       Date:  2018       Impact factor: 1.451

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  2 in total

1.  Tumor-Like Brain Lesions Associated With Variants of Uncertain Significance Compared to Previous Studies: A Case Report.

Authors:  José Omar Santellán-Hernández; Gerardo Romero-Luna; Jacqueline Ramírez-Cruz; Keren Magaly Aguilar-Hidalgo; Sonia Iliana Mejía-Pérez
Journal:  Cureus       Date:  2022-07-14

2.  Optical coherence tomography angiography biomarkers of microvascular alterations in RVCL-S.

Authors:  Mays Al-Nofal; Irene de Boer; Seda Agirman; Anne E Wilms; Amir H Zamanipoor Najafabadi; Gisela M Terwindt; Irene C Notting
Journal:  Front Neurol       Date:  2022-08-26       Impact factor: 4.086

  2 in total

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