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LetterLetter

Cerebellar Atrophy in Craniofacial Morphea: A Report of 2 Cases with 1-year Neuroimaging Followup

RYAN T. LEWINSON, VIMAL H. PRAJAPATI and NADIA J. LUCA
The Journal of Rheumatology September 2020, 47 (9) 1452-1453; DOI: https://doi.org/10.3899/jrheum.190808
RYAN T. LEWINSON
Division of Dermatology, Department of Medicine, University of Calgary;
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VIMAL H. PRAJAPATI
Division of Dermatology, Department of Medicine, Section of Community Pediatrics, Section of Pediatric Rheumatology, Department of Pediatrics, University of Calgary, Dermatology Research Institute;
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NADIA J. LUCA
Section of Pediatric Rheumatology, Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.
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  • For correspondence: nadia.luca@ahs.ca
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    Figure 1.

    Case 1. A. Clinical image showing atrophic, indurated, hyperpigmented, and slightly erythematous plaques involving the scalp and face, consistent with en coup de sabre scleroderma subtype of linear morphea. B. Axial T2-weighted post-gadolinium MRI image showing subtle right cerebellar hemisphere atrophy compared to the left cerebellar hemisphere, with associated parenchymal enhancement in the right cerebellar hemisphere. MRI: magnetic resonance imaging.

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    Figure 2.

    Case 2. A. Clinical image showing subtle right facial asymmetry and significant right tongue atrophy, consistent with Parry-Romberg syndrome subtype of linear morphea. B. Sagittal T1-weighted MRI showing significant vermian atrophy. MRI: magnetic resonance imaging.

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The Journal of Rheumatology
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1 Sep 2020
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Cerebellar Atrophy in Craniofacial Morphea: A Report of 2 Cases with 1-year Neuroimaging Followup
RYAN T. LEWINSON, VIMAL H. PRAJAPATI, NADIA J. LUCA
The Journal of Rheumatology Sep 2020, 47 (9) 1452-1453; DOI: 10.3899/jrheum.190808

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Cerebellar Atrophy in Craniofacial Morphea: A Report of 2 Cases with 1-year Neuroimaging Followup
RYAN T. LEWINSON, VIMAL H. PRAJAPATI, NADIA J. LUCA
The Journal of Rheumatology Sep 2020, 47 (9) 1452-1453; DOI: 10.3899/jrheum.190808
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