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Health-related quality of life, cognitive functioning and behaviour problems in children with Langerhans cell histiocytosis
Authors:Vrijmoet-Wiersma C M Jantien  Kooloos Vicky M  Koopman Hendrik M  Kolk Annemarie M  van der Laan Ingrid  Grootenhuis Martha A  Egeler R Maarten
Affiliation:Department of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands.
Abstract:Gastrointestinal malignancies are extremely rare in the pediatric population, and duodenal cancers represent an even more unusual entity. Intestinal cancers in young adults and children have been observed to be associated with functional deficiencies of the mismatch repair (MMR) system causing a cancer‐predisposition syndrome. We report the case of a 16‐year‐old female with duodenal adenocarcinoma and past history of medulloblastoma found to have a novel germline bialleleic truncating mutation (c.[949C>T]+[949C>T]) of the PMS2 gene. Pediatr Blood Cancer 2009;53:116–120. © 2009 Wiley‐Liss, Inc.
Keywords:biallelic  children and young adults  duodenal adenocarcinoma  mismatch repair
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