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CTNNB1 somatic mutations drive Wnt pathway activation in a case of incidental intranodal palisaded myofibroblastoma.

Abstract
Intranodal palisaded myofibroblastoma (IPM) is a rare stroma-derived spindle-cell neoplasm of the lymph node with myofibroblastic differentiation and CTNNB1 (β-catenin gene) somatic mutations. We present a case of IPM found incidentally in the staging of lung adenocarcinoma. We describe the major histopathological and phenotypic features, including a palisaded bland spindle cell proliferation with myofibroblastic differentiation and Wnt pathway activation by immunohistochemistry, including β-catenin expression. Production of osteoid-like collagen directly from tumor cells was observed. We confirmed p.Gly34Arg CTNNB1 mutation by direct sequencing. We also reviewed the literature for similar cases.
AuthorsGermán Moreno de Juan, Santiago Montes Moreno
JournalRevista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia (Rev Esp Patol) 2023 Oct-Dec Vol. 56 Issue 4 Pg. 279-283 ISSN: 1988-561X [Electronic] Spain
PMID37879826 (Publication Type: Case Reports)
CopyrightCopyright © 2023 Sociedad Española de Anatomía Patológica. Publicado por Elsevier España, S.L.U. All rights reserved.
Chemical References
  • beta Catenin
  • CTNNB1 protein, human
Topics
  • Humans
  • beta Catenin (genetics, metabolism)
  • Wnt Signaling Pathway (genetics)
  • Lymph Nodes (pathology)
  • Neoplasms, Muscle Tissue (genetics, metabolism, pathology)
  • Mutation

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