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Primary Oropharyngeal SMARCA4-Deficient Carcinoma: Expanding the Diagnostic Spectrum in Head and Neck Cancer
Sunil Pasricha1, Sumit Goyal2, Meenakshi Kamboj1
1Department of Histopathology and Cytopathology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, 110085, India.
Abstract:
With the advent of molecular immunohistochemistry and next generation sequencing, Switch/sucrose non-fermentable (SWI/SNF) chromatin remodeling complex altered tumors have gained recognition recently. SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily B member 1 (SMARCB1) and SMARCA4 are the primary SWI/SNF components altered in several recently described undifferentiated malignancies in head and neck region with predilection for paranasal sinuses in SMARCB1-deficient tumors and nasal cavity in SMARCA4-deficient tumors. However, to the best of our knowledge, SMARCA4-deficient tumors of the oropharynx have not been described. We present an unusual case of SMARCA4-deficient carcinoma of the oropharynx (palatine tonsil) which is the first case in the literature, expanding the topographic distribution of SMARCA4-deficient tumors in the head and neck region and emphasizing the importance of BRG1 as an essential immunohistochemical marker for the diagnosis of this distinct entity.
Insights
This study identifies the first known case of SMARCA4-deficient carcinoma in the oropharynx. This finding expands the known locations of Switch/sucrose non-fermentable (SWI/SNF) chromatin remodeling complex related tumors.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Alterations in the Switch/sucrose non-fermentable (SWI/SNF) chromatin remodeling complex are increasingly recognized in various cancers.
- SMARCB1 and SMARCA4 are key SWI/SNF components frequently altered in undifferentiated head and neck malignancies.
- SMARCB1-deficient tumors often occur in the paranasal sinuses, while SMARCA4-deficient tumors typically affect the nasal cavity.
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