Artikel ; Online: CTNNB1 somatic mutations drive Wnt pathway activation in a case of incidental intranodal palisaded myofibroblastoma.
2023 Band 56, Heft 4, Seite(n) 279–283
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 ...
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. |
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Mesh-Begriff(e) | Humans ; beta Catenin/genetics ; beta Catenin/metabolism ; Wnt Signaling Pathway/genetics ; Lymph Nodes/pathology ; Neoplasms, Muscle Tissue/genetics ; Neoplasms, Muscle Tissue/metabolism ; Neoplasms, Muscle Tissue/pathology ; Mutation |
Chemische Substanzen | beta Catenin ; CTNNB1 protein, human |
Sprache | Englisch |
Erscheinungsdatum | 2023-05-01 |
Erscheinungsland | Spain |
Dokumenttyp | Case Reports |
ZDB-ID | 2463888-2 |
ISSN | 1988-561X ; 1988-561X |
ISSN (online) | 1988-561X |
ISSN | 1988-561X |
DOI | 10.1016/j.patol.2023.02.003 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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