1. Plexiform Fibromyxoma in the Stomach: Immunohistochemical Profile and Comprehensive Genetic Characterization.
- Author
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Di Mauro A, Rega RA, Leongito M, Albino V, Palaia R, Gualandi A, Belli A, D'Arbitrio I, Moccia P, Tafuto S, De Chiara A, Ottaiano A, and Ferrara G
- Subjects
- Humans, Male, Aged, Immunohistochemistry, Mutation, Biomarkers, Tumor genetics, Gastrectomy, Stomach Neoplasms genetics, Stomach Neoplasms pathology, Stomach Neoplasms surgery, Stomach Neoplasms metabolism, Fibroma genetics, Fibroma pathology, Fibroma metabolism
- Abstract
Plexiform fibromyxoma (PF), also referred to as plexiform angiomyxoid myofibroblast tumor, is an exceedingly rare mesenchymal neoplasm primarily affecting the stomach. Herein, we present a case of PF diagnosed in a 71-year-old male with a history of lung cancer, initially suspected to have a gastrointestinal stromal tumor (GIST) of the stomach, who subsequently underwent subtotal gastrectomy. The histopathological and molecular features of the tumor, including mutations in ABL1 , CCND1 , CSF1R , FGFR4 , KDR , and MALAT1-GLI1 fusion, are elucidated and discussed in the context of diagnostic, prognostic, and therapeutic considerations.
- Published
- 2024
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