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pubmed-article:17438222pubmed:abstractTextWe present one patient with Parry Romberg syndrome and another with linear scleroderma in coup de sabre, with focal neurologic deficits and intractable seizures arising from the hemisphere ipsilateral to the cutaneous lesion. Brain MRI showed progressive hemispheric atrophy. Pathology after functional hemispherectomy showed chronic inflammatory features suggestive of Rasmussen encephalitis.lld:pubmed
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pubmed-article:17438222pubmed:articleTitleParry Romberg syndrome and linear scleroderma in coup de sabre mimicking Rasmussen encephalitis.lld:pubmed
pubmed-article:17438222pubmed:affiliationDepartment of Neurology, Hospital Clínic, Barcelona, Spain. mcarreno@clinic.ub.eslld:pubmed
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