Spindle Cell Lesions with Oncogenic EGFR Kinase Domain Aberrations: Expanding the Spectrum of Protein Kinase-Related Mesenchymal Tumors.
Silvia ValleseSabina BarresiLaura Hiemcke-JiwaSara PatriziLennart KesterIsabella GiovannoniAntonello CardoniLucia PedaceClaudia NardiniChantal TancrediMartina DesideriAndreas von DeimlingRosa M MuraMichela PigaMaria E ErricoAlessandra StracuzziRita AlaggioEvelina MieleUta FluckePublished in: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc (2024)
EGFR aberrations are reported in a subset of myofibroblastic lesions with kinase domain duplication (EGFR-KDD) and exon 20 mutations being assigned to infantile fibrosarcomas (IFS), mesoblastic nephroma, and fibrous hamartoma of infancy (FHI), respectively. In this retrospective study, we correlated molecular findings with the histomorphology of 14 myofibroblastic lesions harboring such genetic changes identified by NGS. We additionally performed DNA methylation profiling (DNAmp) and immunohistochemistry. Lesions were from 10 males and 4 females with a mean age of 3 years (range, 0.3-14) and occurred subcutaneously in the upper limbs (n = 5), lower limbs (n = 3), back/thorax (n = 5), and the nasal cavity (n = 1). Eleven were cured by surgery, including 1 relapsed case. Two patients were lost to follow-up. One case was very recent, and the patient was biopsied. Histologically, the lesions showed a wide spectrum varying from classic FHI (n = 9) to IFS (n = 1) or lipofibromatosis-like tumors (LFT-like) (n = 2) or dermatofibrosarcoma protuberans-like (DFSP-like) (n = 1) to a predominantly myxoid spindle cell lesion (n = 1). Immunohistochemically, all neoplasms stained with CD34, whereas S100 was positive in 2/14. EGFR expression was observed in 9/10 cases. Molecularly, the IFS and 1 LFT-like harbored EGFR-KDD, whereas an exon 20 mutation was identified in all FHI, 1 LFT-like, the DFSP-like, and in predominant myxoid spindle cell lesion. By DNAmp, all but 2 cases formed a well-defined cluster, demonstrating that these lesions are also epigenetically related. In conclusion, EGFR kinase domain aberrations found in FHI, IFS, LFT-like, DFSP-like, and a spindle cell lesion with a predominant myxoid stroma of children and adolescents showed that these neoplasms with a broad morphologic spectrum belong to the group of protein kinase-related lesions with a distinct epigenetic signature. Molecular analyses, including DNAmp, help to identify and characterize this emerging category and become mandatory when targeted treatment is considered.
Keyphrases
- tyrosine kinase
- small cell lung cancer
- epidermal growth factor receptor
- protein kinase
- single cell
- dna methylation
- cell therapy
- copy number
- gene expression
- stem cells
- genome wide
- newly diagnosed
- ejection fraction
- end stage renal disease
- bone marrow
- case report
- drug delivery
- peritoneal dialysis
- multiple myeloma
- atrial fibrillation
- replacement therapy
- coronary artery disease
- single molecule
- smoking cessation
- patient reported outcomes
- long non coding rna
- prognostic factors
- weight loss
- combination therapy