Literature DB >> 12963929

Scleroderma en coup de sabre with central nervous system and ophthalmologic involvement: treatment of ocular symptoms with interferon gamma.

Gerlinde Obermoser1, Bettina E Pfausler, Dennis M Linder, Norbert T Sepp.   

Abstract

Scleroderma en coup de sabre, a variant of localized scleroderma, is a disorder of unknown origin characterized by fibrosis of connective tissue. Rare complications of scleroderma en coup de sabre are orbital and intracerebral involvement. We describe a patient with scleroderma en coup de sabre in whom intracerebral and orbital lesions developed after 2 decades of disease duration. Clinically, she had epilepsy, impaired vision, and retro-ocular pain of the affected eye. A 12-month course of interferon-gamma stopped progression of visual symptoms caused by orbital fibrous tissue. To our knowledge, this is the first patient with scleroderma en coup de sabre complicated by orbital involvement who was successfully treated with interferon-gamma.

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Year:  2003        PMID: 12963929     DOI: 10.1067/s0190-9622(03)00901-0

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  10 in total

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2.  Frontal linear scleroderma en coup de sabre associated with epileptic seizure.

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3.  Difficulties in differentiation of Parry-Romberg syndrome, unilateral facial sclerodermia, and Rasmussen syndrome.

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4.  Ocular involvement in children with localised scleroderma: a multi-centre study.

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6.  CNS imaging findings associated with Parry-Romberg syndrome and en coup de sabre: correlation to dermatologic and neurologic abnormalities.

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7.  Neurologic involvement in scleroderma en coup de sabre.

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Review 9.  Localized scleroderma: clinical spectrum and therapeutic update.

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10.  Neuroimaging findings of linear scleroderma of the head and face: a case report.

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  10 in total

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