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REVERSIBLE POSTERIOR LEUCOENCEPHALOPATHY IN AN 11 YEAR-OLD MALE CHILD

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dc.contributor.author Tabel, Y
dc.contributor.author Akin, IM
dc.contributor.author Gungor, S
dc.contributor.author Karakurt, C
dc.contributor.author Ozgen, U
dc.date.accessioned 2022-10-19T08:16:14Z
dc.date.available 2022-10-19T08:16:14Z
dc.date.issued 2010
dc.identifier.uri http://hdl.handle.net/11616/81829
dc.description.abstract Systemic lupus erythematosus is a chronic inflammatory disease characterized by highly diverse clinical manifestations. The major organ system involvements in childhood systemic lupus erythematosus are similar to those found in adults. Recognizing and reversing secondary causes of central nervous system abnormalities in patients with systemic lupus erythematosus are essential for preventing long-term neurologic disability or death.
dc.description.abstract In this manuscript, we present an 11 year-old male followed up in our clinic, who had the very rare involvement and complications of systemic lupus erythematosus in childhood. He developed a reversible posterior leucoencephalopathy after the first dose of cyclophosphamide, but cyclophosphamide therapy was not stopped as there was no clear evidence in the literature related to the role of this drug in reversible posterior leucoencephalopathy. The patient has now recovered.
dc.description.abstract C1 [Tabel, Yilmaz; Akin, Ilke Mungan; Gungor, Serdal; Karakurt, Cemsit; Ozgen, Unsal] Inonu Univ, Tip Fak, Pediat Anabilim Dali, Malatya, Turkey.
dc.source MARMARA MEDICAL JOURNAL
dc.title REVERSIBLE POSTERIOR LEUCOENCEPHALOPATHY IN AN 11 YEAR-OLD MALE CHILD


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