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From the Departments of Neurology (M.C., A.D., M.F., R.A.), Pathology (T.R.), Neurosurgery (J.R.), Radiology (N.B.), Nuclear Medicine (X.S.), Neuropsychology (T.B., A.R.), and Psychiatry (L.P.), H. Clínic, Barcelona, Spain; and Department of Neurology (M.I.B.), Hospital Son Dureta, Palma de Mallorca, Spain.
Address correspondence and reprint requests to Dr. Mar Carreño, Department of Neurology, Hospital Clínic, Barcelona, Spain; e-mail: mcarreno{at}clinic.ub.es
We 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.
Disclosure: The authors report no conflicts of interest.
Received April 26, 2006. Accepted in final form December 11, 2006.
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