Publication:
Nephroblastomatosis or Wilms Tumor in a Fourth Patient With a Somatic PIK3CA Mutation

dc.contributor.other Integrated Molecular Plant physiology Research (IMPRES)
dc.date.accessioned 2019-04-26T08:57:26Z
dc.date.available 2019-04-26T08:57:26Z
dc.date.issued 18/05/16
dc.description Wilms tumor and nephroblastomatosis are associated with syndromic conditions including hemihyperplasia. Hemihyperplasia is genetically heterogeneous and may be the result of genomic abnormalities seen in Beckwith–Wiedemann syndrome, mosaic chromosome or genomic abnormalities, or somatic point mutations. Somatic missense mutations affecting the PI3K-AKT-MTOR pathway result in segmental overgrowth and are present in numerous benign and malignant tumors. Here, we report a fourth patient with asymmetric overgrowth due to a somatic PIK3CA mutation who had nephroblastomatosis or Wilms tumor. Similar to two of three reported patients with a somatic PIK3CA mutation and renal tumors, he shared a PIK3CA mutation affecting codon 1047, presented at birth with asymmetric overgrowth, and had fibroadipose overgrowth. Codon 1047 is most commonly affected by somatic mutations in PIK3CA-related overgrowth spectrum (PROS). While the fibroadipose overgrowth phenotype appears to be common in individuals with PIK3CA mutations at codon 1047, individuals with a clinical diagnosis of Klippel–Trenaunay syndrome or isolated lymphatic malformation also had mutations affecting this amino acid. Screening for Wilms tumor in individuals with PROS-related hemihyperplasia may be considered and, until the natural history is fully elucidated in larger cohort studies, may follow guidelines for Beckwith–Wiedemann syndrome, or isolated hemihyperplasia. It is not known if the specific PIK3CA mutation, the mosaic distribution, or the clinical presentation affect the Wilms tumor or nephroblastomatosis risk in individuals with PROS.
dc.ejemplo3.0.ejem Gripp, Karen W
dc.ejemplo3.0.ejem Baker, Laura
dc.ejemplo3.0.ejem Kandula, Vinay
dc.ejemplo3.0.ejem Conard, Katrina
dc.ejemplo3.0.ejem Scavina, Mena
dc.ejemplo3.0.ejem Napoli, Joseph A
dc.ejemplo3.0.ejem Griffin, Gregory C
dc.ejemplo3.0.ejem Thacker, Mihir
dc.ejemplo3.0.ejem Knox, Rachel G
dc.ejemplo3.0.ejem Clark, Graeme
dc.ejemplo3.0.ejem Parker, Victoria ER
dc.ejemplo3.0.ejem Mirzaa, Ghayda
dc.ejemplo3.0.ejem Keppler-Noreuil, Kim M
dc.identifier.uri https://demo7.dspace.org/handle/10673/473
dc.language en
dc.publisher.program Wiley
dc.title Nephroblastomatosis or Wilms Tumor in a Fourth Patient With a Somatic PIK3CA Mutation
dspace.entity.type Publication
relation.isAuthorOfPublication 29d455df-34af-4e5d-abf7-305016ffcafe
relation.isOrgUnitOfPublication e367d914-4102-44d2-8346-4e08c0f08b5f
relation.isProjectOfPublication 5e983159-d5e9-4732-8a8c-e470a2057f71
relation.isProjectOfPublication 6b8acf78-6129-467b-a1bc-54862170c307
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