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J Clin Pathol ; 76(12): 802-812, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37550012

ABSTRACT

New tumour types are being described at increasing frequency, and most new tumour types are now identified via retrospective review of next-generation sequencing data. This contrasts with the traditional, morphology-based method of identifying new tumour types, and while the sequencing-based approach has accelerated progress in the field, it has also introduced novel and under-recognised biases. Here, we discuss tumour types identified based on morphology, including superficial CD34-positive fibroblastic tumour, pseudoendocrine sarcoma and cutaneous clear cell tumour with melanocytic differentiation and ACTIN::MITF fusion. We also describe tumour types identified primarily by next-generation sequencing, including epithelioid and spindle cell rhabdomyosarcoma, round cell neoplasms with EWSR1::PATZ1 fusion, cutaneous melanocytic tumour with CRTC1::TRIM11 fusion, clear cell tumour with melanocytic differentiation and MITF::CREM fusion and GLI1-altered mesenchymal neoplasms, including nested glomoid neoplasm.


Subject(s)
Sarcoma , Skin Neoplasms , Soft Tissue Neoplasms , Adult , Humans , Child , Skin Neoplasms/pathology , Soft Tissue Neoplasms/pathology , Transcription Factors/genetics , Transcription Factors/metabolism , Sarcoma/genetics , Sarcoma/pathology , Bias , Biomarkers, Tumor/genetics , Repressor Proteins , Kruppel-Like Transcription Factors , Tripartite Motif Proteins/metabolism , Ubiquitin-Protein Ligases/metabolism
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