Literature DB >> 29051208

Redefining the Pulvinar Sign in Fabry Disease.

S Cocozza1, C Russo2, A Pisani3, G Olivo4, E Riccio3, A Cervo1, G Pontillo1,5, S Feriozzi6, M Veroux7, Y Battaglia8, D Concolino9, F Pieruzzi10, R Mignani11, P Borrelli12, M Imbriaco1, A Brunetti1, E Tedeschi1, G Palma1.   

Abstract

BACKGROUND AND
PURPOSE: The pulvinar sign refers to exclusive T1WI hyperintensity of the lateral pulvinar. Long considered a common sign of Fabry disease, the pulvinar sign has been reported in many pathologic conditions. The exact incidence of the pulvinar sign has never been tested in representative cohorts of patients with Fabry disease. The aim of this study was to assess the prevalence of the pulvinar sign in Fabry disease by analyzing T1WI in a large Fabry disease cohort, determining whether relaxometry changes could be detected in this region independent of the pulvinar sign positivity.
MATERIALS AND METHODS: We retrospectively analyzed brain MR imaging of 133 patients with Fabry disease recruited through specialized care clinics. A subgroup of 26 patients underwent a scan including 2 FLASH sequences for relaxometry that were compared with MRI scans of 34 healthy controls.
RESULTS: The pulvinar sign was detected in 4 of 133 patients with Fabry disease (3.0%). These 4 subjects were all adult men (4 of 53, 7.5% of the entire male population) with renal failure and under enzyme replacement therapy. When we tested for discrepancies between Fabry disease and healthy controls in quantitative susceptibility mapping and relaxometry maps, no significant difference emerged for any of the tested variables.
CONCLUSIONS: The pulvinar sign has a significantly lower incidence in Fabry disease than previously described. This finding, coupled with a lack of significant differences in quantitative MR imaging, allows hypothesizing that selective involvement of the pulvinar is a rare neuroradiologic sign of Fabry disease.
© 2017 by American Journal of Neuroradiology.

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Year:  2017        PMID: 29051208      PMCID: PMC7963734          DOI: 10.3174/ajnr.A5420

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


  40 in total

1.  Profile of endothelial and leukocyte activation in Fabry patients.

Authors:  T DeGraba; S Azhar; F Dignat-George; E Brown; B Boutière; G Altarescu; R McCarron; R Schiffmann
Journal:  Ann Neurol       Date:  2000-02       Impact factor: 10.422

2.  Increased signal intensity in the pulvinar on T1-weighted images: a pathognomonic MR imaging sign of Fabry disease.

Authors:  David F Moore; Frank Ye; Raphael Schiffmann; John A Butman
Journal:  AJNR Am J Neuroradiol       Date:  2003 Jun-Jul       Impact factor: 3.825

3.  Nervous system involvement in Fabry's disease: clinicopathological and biochemical correlation.

Authors:  E M Kaye; E H Kolodny; E L Logigian; M D Ullman
Journal:  Ann Neurol       Date:  1988-05       Impact factor: 10.422

4.  Brain lesions in alcoholics. A neuropathological study with clinical correlations.

Authors:  A Torvik; C F Lindboe; S Rogde
Journal:  J Neurol Sci       Date:  1982-11       Impact factor: 3.181

5.  Basilar Artery Changes in Fabry Disease.

Authors:  R Manara; R Y Carlier; S Righetto; V Citton; G Locatelli; F Colas; M Ermani; D P Germain; A Burlina
Journal:  AJNR Am J Neuroradiol       Date:  2017-01-26       Impact factor: 3.825

6.  Cerebrovascular complications of Fabry's disease.

Authors:  P Mitsias; S R Levine
Journal:  Ann Neurol       Date:  1996-07       Impact factor: 10.422

Review 7.  The cerebral vasculopathy of Fabry disease.

Authors:  David F Moore; Christine R Kaneski; Hasan Askari; Raphael Schiffmann
Journal:  J Neurol Sci       Date:  2007-03-23       Impact factor: 3.181

8.  High signal intensity in the dentate nucleus and globus pallidus on unenhanced T1-weighted MR images: relationship with increasing cumulative dose of a gadolinium-based contrast material.

Authors:  Tomonori Kanda; Kazunari Ishii; Hiroki Kawaguchi; Kazuhiro Kitajima; Daisuke Takenaka
Journal:  Radiology       Date:  2013-12-07       Impact factor: 11.105

Review 9.  Fabry disease.

Authors:  Dominique P Germain
Journal:  Orphanet J Rare Dis       Date:  2010-11-22       Impact factor: 4.123

10.  A Novel Multiparametric Approach to 3D Quantitative MRI of the Brain.

Authors:  Giuseppe Palma; Enrico Tedeschi; Pasquale Borrelli; Sirio Cocozza; Carmela Russo; Saifeng Liu; Yongquan Ye; Marco Comerci; Bruno Alfano; Marco Salvatore; E Mark Haacke; Marcello Mancini
Journal:  PLoS One       Date:  2015-08-18       Impact factor: 3.240

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  8 in total

Review 1.  Heritable and non-heritable uncommon causes of stroke.

Authors:  A Bersano; M Kraemer; A Burlina; M Mancuso; J Finsterer; S Sacco; C Salvarani; L Caputi; H Chabriat; S Lesnik Oberstein; A Federico; E Tournier Lasserve; D Hunt; M Dichgans; M Arnold; S Debette; H S Markus
Journal:  J Neurol       Date:  2020-04-21       Impact factor: 4.849

Review 2.  Pulvinar Sign, Stroke and Their Relationship with Fabry Disease: A Systematic Review and Metanalysis.

Authors:  Juan Fernando Ortíz; María Belén Solís; Syed Saad Ali; Mahika Khurana; Juan Andrés Moncayo; Nishel Yogesh Kothari; Mateo Alzamora; Ahmed Eissa-Garces; Ghanshyam Patel; Gustavo Andrés Monteros; Meghdeep Sen; Jonathan Quiñonez
Journal:  Neurol Int       Date:  2022-06-01

Review 3.  Neuroimaging in Fabry disease: current knowledge and future directions.

Authors:  Sirio Cocozza; Camilla Russo; Giuseppe Pontillo; Antonio Pisani; Arturo Brunetti
Journal:  Insights Imaging       Date:  2018-11-02

4.  Characteristics of Neurological Symptoms in Adult Japanese Patients with Fabry Disease.

Authors:  Jun Sawada; Naoki Nakagawa; Kohei Kano; Tsukasa Saito; Takayuki Katayama; Takaaki Sawada; Ken Momosaki; Kimitoshi Nakamura; Naoyuki Hasebe
Journal:  Intern Med       Date:  2021-01-15       Impact factor: 1.271

5.  Neuroradiological differentiation of white matter lesions in patients with multiple sclerosis and Fabry disease.

Authors:  Jakob Rath; Olivia Foesleitner; Lukas Haider; Hubert Bickel; Fritz Leutmezer; Stephan Polanec; Michael A Arnoldner; Gere Sunder-Plassmann; Daniela Prayer; Thomas Berger; Paulus Rommer; Gregor Kasprian
Journal:  Orphanet J Rare Dis       Date:  2022-02-05       Impact factor: 4.123

6.  Neuropsychiatric Symptoms and Their Association With Sex, Age, and Enzyme Replacement Therapy in Fabry Disease: A Systematic Review.

Authors:  Magdalena Mroczek; Ignazio Maniscalco; Manon Sendel; Ralf Baron; Erich Seifritz; Albina Nowak
Journal:  Front Psychiatry       Date:  2022-03-16       Impact factor: 4.157

7.  RESUME: Turning an SWI acquisition into a fast qMRI protocol.

Authors:  Serena Monti; Pasquale Borrelli; Enrico Tedeschi; Sirio Cocozza; Giuseppe Palma
Journal:  PLoS One       Date:  2017-12-20       Impact factor: 3.240

8.  Absence of infratentorial lesions in Fabry disease contributes to differential diagnosis with multiple sclerosis.

Authors:  Lorenzo Ugga; Sirio Cocozza; Giuseppe Pontillo; Camilla Russo; Vincenzo Brescia Morra; Roberta Lanzillo; Eleonora Riccio; Antonio Pisani; Arturo Brunetti
Journal:  Brain Behav       Date:  2018-10-02       Impact factor: 2.708

  8 in total

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