Madana J, Yolmo Deeke, Gopalakrishnan S, Saxena Sunil Kumar
Department of Otorhinolaryngology-Head and Neck Surgery, National University Health System, Republic of Singapore 119228.
Ear Nose Throat J. 2011 Oct;90(10):E4-7. doi: 10.1177/014556131109001016.
Paranasal sinus carcinoma is rare, with an estimated annual incidence of less than 1 per 100,000 population. Primary frontal sinus involvement is extremely rare, accounting for only 0.3% of all paranasal sinus malignancies. A frontal sinus cancer may be mistaken for a mucocele, pyocele, or osteomyelitis. We report the case of a 48-year-old woman with a carcinoma that originated in the frontal sinus. Computed tomography and magnetic resonance imaging demonstrated bony destruction with intracranial extension but no involvement of the bulbus. The patient underwent a frontal craniotomy, tumor excision, and postoperative radiotherapy. One year later, she remained symptom-free.
鼻窦癌较为罕见,估计年发病率低于十万分之一。原发性额窦受累极为罕见,仅占所有鼻窦恶性肿瘤的0.3%。额窦癌可能被误诊为黏液囊肿、脓性囊肿或骨髓炎。我们报告一例起源于额窦的48岁女性癌症病例。计算机断层扫描和磁共振成像显示骨质破坏并向颅内扩展,但眼球未受累。该患者接受了额部开颅手术、肿瘤切除及术后放疗。一年后,她仍无症状。