SMARCB1 (INI1)‐deficient sinonasal carcinoma manifesting as oral lesions: A report of two cases

上颌骨 医学 SMARCB1型 病理 头颈部 鉴别诊断 解剖 外科 生物 遗传学 染色质 染色质重塑 DNA
作者
Jessie Fuoco,Michelle Huang,Najmeh Esfandiari,Christina MacMillan,Aiman Ali,Kanan Dave,Marshall Freilich,Marco Magalhaes
出处
期刊:Head & neck [Wiley]
卷期号:46 (3): E32-E39 被引量:2
标识
DOI:10.1002/hed.27595
摘要

Abstract Background Sinonasal carcinomas represent a rare group of malignancies, accounting for less than 5% of all head and neck cancers and a worldwide incidence of less than 1 case per 100 000 inhabitants annually. Despite the restricted anatomical location, sinonasal carcinomas harbor some of the most histologically and molecularly diverse groups of tumors. SMARCB1 (INI1)‐deficient sinonasal carcinomas are locally aggressive tumors commonly detected late, leading to devastating morbidity and mortality. Case Report We present two cases of SMARCB1‐deficient sinonasal carcinoma involving the oral cavity and presenting as progressive radiolucent lesions with local swelling associated with maxillary dentition and alveolar bone. Both cases were initially considered odontogenic in origin and involved the destruction of the left anterior maxilla. Conclusion Given the rarity and the variable presentation of these tumors, they pose a challenge for head and neck surgeons, dentists, and pathologists due to the potential overlapping features with odontogenic and non‐odontogenic inflammatory and neoplastic lesions. These cases highlight the importance of a multidisciplinary team and include SMARCB1‐deficient sinonasal carcinomas in the differential diagnosis of destructive lesions of the maxilla.

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