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Journal Article
Review
Top IHC/ISH Hacks for and Molecular Surrogates of Poorly Differentiated Sinonasal Small Round Cell Tumors.
Head and Neck Pathology 2024 Februrary 6
BACKGROUND: Poorly differentiated sinonasal small round cell tumors (SRCTs) are rare and heterogeneous, posing challenges in diagnosis and treatment.
METHODS: Recent advances in molecular findings and diagnostic refinement have promoted better understanding and management of these tumors.
RESULTS: The newly defined and emerging sinonasal entities demonstrate diverse morphologies, specific genomic signatures, and clinical behavior from conventional counterparts. In this review of SRCTs, emphasis is placed on the diagnostic approach with the employment of a pertinent panel of immunohistochemistry studies and/or molecular tests, fine-tuned to the latest WHO 5 classification of sinonasal/paranasal tumors and personalized treatment.
CONCLUSION: Specifically, this review focuses on tumors with epithelial and neuroectodermal derivation.
METHODS: Recent advances in molecular findings and diagnostic refinement have promoted better understanding and management of these tumors.
RESULTS: The newly defined and emerging sinonasal entities demonstrate diverse morphologies, specific genomic signatures, and clinical behavior from conventional counterparts. In this review of SRCTs, emphasis is placed on the diagnostic approach with the employment of a pertinent panel of immunohistochemistry studies and/or molecular tests, fine-tuned to the latest WHO 5 classification of sinonasal/paranasal tumors and personalized treatment.
CONCLUSION: Specifically, this review focuses on tumors with epithelial and neuroectodermal derivation.
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