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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Authors | Germán Moreno de Juan, Santiago Montes Moreno |
Journal | Revista 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 |
PMID | 37879826
(Publication Type: Case Reports)
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Copyright | Copyright © 2023 Sociedad Española de Anatomía Patológica. Publicado por Elsevier España, S.L.U. All rights reserved. |
Chemical References |
- beta Catenin
- CTNNB1 protein, human
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Topics |
- Humans
- beta Catenin
(genetics, metabolism)
- Wnt Signaling Pathway
(genetics)
- Lymph Nodes
(pathology)
- Neoplasms, Muscle Tissue
(genetics, metabolism, pathology)
- Mutation
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