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   <subfield code="a">Children with posterior reversible encephalopathy syndrome associated with atypical diffusion-weighted imaging and apparent diffusion coefficient</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Kenji Ishikura, Yuko Hamasaki, Tomoyuki Sakai, Hiroshi Hataya, Tomohide Goto, Sahoko Miyama, Tatsuo Kono, Masataka Honda]</subfield>
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   <subfield code="a">Posterior reversible encephalopathy syndrome (PRES) is a reversible, predominantly posterior, leukoencephalopathy associated with renal insufficiency, hypertension, or immunosuppressant drugs. We describe two children with PRES whose primary diagnoses were idiopathic nephrotic syndrome and lupus nephritis. Cranial magnetic resonance (MR) imaging at the onset of PRES showed strong hyperintense signals on diffusion-weighted imaging with restricted apparent diffusion coefficient values predominantly in the posterior region. Such findings have been rarely reported in children with PRES and initially suggested irreversible brain damage; however, both children fully recovered clinically as well as radiologically. Our findings suggest the limitations of cranial MR imaging for diagnosing PRES. Further experience with cranial MR imaging, including diffusion-weighted imaging with apparent diffusion coefficient mapping, is required to improve diagnostic accuracy and the ability to predict outcomes in patients with early-stage PRES. At present, initial imaging studies do not necessarily provide sufficient evidence for a firm diagnosis of PRES or the prediction of outcomes.</subfield>
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   <subfield code="a">Japanese Society of Nephrology, 2010</subfield>
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   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Apparent diffusion coefficient values</subfield>
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   <subfield code="a">Children</subfield>
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   <subfield code="a">Nephrotic syndrome</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Systemic lupus erythematosus</subfield>
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   <subfield code="a">Ishikura</subfield>
   <subfield code="D">Kenji</subfield>
   <subfield code="u">Department of Pediatric Nephrology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, 183-8561, Fuchu, Tokyo, Japan</subfield>
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   <subfield code="a">Hamasaki</subfield>
   <subfield code="D">Yuko</subfield>
   <subfield code="u">Department of Pediatric Nephrology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, 183-8561, Fuchu, Tokyo, Japan</subfield>
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   <subfield code="a">Sakai</subfield>
   <subfield code="D">Tomoyuki</subfield>
   <subfield code="u">Department of Pediatric Nephrology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, 183-8561, Fuchu, Tokyo, Japan</subfield>
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   <subfield code="a">Hataya</subfield>
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   <subfield code="u">Department of Pediatric Nephrology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, 183-8561, Fuchu, Tokyo, Japan</subfield>
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   <subfield code="a">Goto</subfield>
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   <subfield code="u">Department of Pediatric Neurology, Tokyo Metropolitan Children's Medical Center, Fuchu, Japan</subfield>
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   <subfield code="a">Miyama</subfield>
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   <subfield code="u">Department of Pediatric Neurology, Tokyo Metropolitan Children's Medical Center, Fuchu, Japan</subfield>
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   <subfield code="a">Kono</subfield>
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   <subfield code="u">Department of Pediatric Radiology, Tokyo Metropolitan Children's Medical Center, Fuchu, Japan</subfield>
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   <subfield code="a">Honda</subfield>
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   <subfield code="u">Department of Pediatric Nephrology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, 183-8561, Fuchu, Tokyo, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="t">Clinical and Experimental Nephrology</subfield>
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   <subfield code="B">NATIONALLICENCE</subfield>
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