Anila K R, Ginju V, Vishnu V L, Kumar Rejnish, Jayasree K
Department of Pathology, Regional Cancer Centre, Thiruvananthapuram, Kerala, India.
Department of Radiation Oncology, Regional Cancer Centre, Thiruvananthapuram, Kerala, India.
Indian J Pathol Microbiol. 2023 Jan-Mar;66(1):159-161. doi: 10.4103/ijpm.ijpm_77_22.
SMARCB1 deficient sinonasal carcinomas are rare neoplasms, classified under sinonasal undifferentiated carcinomas by the fourth edition of the World Health Organization (WHO) classification of head and neck tumors. It is characterized immunohistochemically by loss of SMARCB1(INI1) expression. We are reporting the case of a 63-year-old man who was evaluated for nasal stuffiness of 3 months duration in another hospital where a radiological evaluation showed a polypoidal soft tissue lesion in the right maxillary sinus extending to the right nasal cavity and spheno-ethmoidal sinus. He underwent excision biopsy which was reported as non- keratinizing nasopharyngeal carcinoma. He was referred to our center with residual disease in spheno-ethmoidal recess for which radiotherapy was given. After completion of radiotherapy, the primary site had no residual disease, but while on follow-up he developed left sided neck nodes within 4 months of completion of treatment. Excision of the lesion was done and histopathological and immunohistochemical analysis revealed it to be metastasis from SMARCB1 deficient sinonasal carcinoma and not nasopharyngeal carcinoma as diagnosed from the other center. This case is being reported to highlight the diagnostic challenge associated with this rare entity.
SMARCB1缺陷型鼻窦癌是罕见肿瘤,在世界卫生组织(WHO)头颈部肿瘤分类第四版中归类于鼻窦未分化癌。其免疫组化特征为SMARCB1(INI1)表达缺失。我们报告一例63岁男性病例,该患者因持续3个月的鼻塞在另一家医院接受评估,放射学检查显示右侧上颌窦有息肉样软组织病变,延伸至右侧鼻腔和蝶筛窦。他接受了切除活检,报告为非角化性鼻咽癌。因蝶筛隐窝残留病灶,他被转诊至我们中心并接受了放疗。放疗结束后,原发部位无残留病灶,但在随访期间,治疗结束后4个月内他出现了左侧颈部淋巴结肿大。对病灶进行了切除,组织病理学和免疫组化分析显示其为SMARCB1缺陷型鼻窦癌转移灶,而非另一家中心诊断的鼻咽癌。报告该病例是为了突出与这种罕见实体相关的诊断挑战。