Literature DB >> 18830119

Silent white matter lesion in linear scleroderma en coup de sabre.

Mio Sakai1, Shigeki Aoki, Yusuke Inoue, Ryuichi Ashida, Haruyasu Yamada, Shigeru Kiryu, Sachiko Inano, Harushi Mori, Yoshitaka Masutani, Osamu Abe, Kuni Ohtomo, Hironobu Nakamura.   

Abstract

We report a patient with linear scleroderma en coup de sabre without neurological symptoms despite the presence of large white matter lesions. The patient underwent 3.0-T magnetic resonance (MR) examinations including diffusion tensor imaging, time-resolved contrast-enhanced MR angiography, susceptibility-weighted imaging, and proton MR spectroscopy. These imaging findings suggested increased vascular permeability and microbleeding without abnormalities of metabolites. Our observation is consistent with vasculopathy and may be helpful in the proper diagnosis and treatment of linear scleroderma en coup de sabre.

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Year:  2008        PMID: 18830119     DOI: 10.1097/RCT.0b013e318153fd60

Source DB:  PubMed          Journal:  J Comput Assist Tomogr        ISSN: 0363-8715            Impact factor:   1.826


  3 in total

Review 1.  The central nervous system manifestations of localized craniofacial scleroderma: a study of 10 cases and literature review.

Authors:  Ezekiel Maloney; Sarah J Menashe; Ramesh S Iyer; Sarah Ringold; Amit K Chakraborty; Gisele E Ishak
Journal:  Pediatr Radiol       Date:  2018-07-03

2.  A significant proportion of children with morphea en coup de sabre and Parry-Romberg syndrome have neuroimaging findings.

Authors:  Yvonne E Chiu; Sheetal Vora; Eun-Kyung M Kwon; Mohit Maheshwari
Journal:  Pediatr Dermatol       Date:  2012 Nov-Dec       Impact factor: 1.588

3.  Imaging and clinical findings in a case of linear scleroderma en coup de sabre.

Authors:  Conal M Corbally; Andrew Breckenridge; Ravi Jampana
Journal:  BJR Case Rep       Date:  2016-11-02
  3 in total

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