Your browser doesn't support javascript.
loading
Intestinal duplication revealed by posterior reversible encephalopathy syndrome / 소아과
Article in En | WPRIM | ID: wpr-714072
Responsible library: WPRO
ABSTRACT
We report a unique case of intestinal duplication detected on posterior reversible encephalopathy syndrome (PRES) in a 13-year-old girl. She was admitted to the pediatric Emergency Department because of generalized seizures. Radiological assessment revealed a large, well-defined, thick-walled cystic lesion in the mid abdomen, suggestive of duplication cyst associated to a PRES. Exploration confirmed the diagnosis of ileal duplication cyst, and the mass was resected. The postoperative course was uneventful. Both hypertension and neurological dysfunction resolved after the mass resection. A followup brain magnetic resonance imaging was performed 9 months later and showed complete resolution of the cerebellar changes. Although extrinsic compression of the retroperitoneal structures has not been reported in the literature as a complication of duplication cyst, we strongly believe that this is the most logical and plausible hypothesis that would explain the pathogenesis of PRES in our patient.
Subject(s)
Key words
Full text: 1 Index: WPRIM Main subject: Seizures / Brain / Magnetic Resonance Imaging / Follow-Up Studies / Diagnosis / Emergency Service, Hospital / Abdomen / Posterior Leukoencephalopathy Syndrome / Hypertension / Ileum Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Korean Journal of Pediatrics Year: 2018 Type: Article
Full text: 1 Index: WPRIM Main subject: Seizures / Brain / Magnetic Resonance Imaging / Follow-Up Studies / Diagnosis / Emergency Service, Hospital / Abdomen / Posterior Leukoencephalopathy Syndrome / Hypertension / Ileum Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Korean Journal of Pediatrics Year: 2018 Type: Article