Naito Shoji, Yokoi Hidenori, Matsumoto Yuma, Kawada Michitsugu, Inomata Kohei, Fujiwara Masachika, Ohara Arisa, Saito Koichiro
Department of Otolaryngology-Head and Neck Surgery, Kyorin University School of Medicine, Tokyo 181-8611, Japan.
Department of Pathology, Kyorin University School of Medicine, Tokyo 181-8611, Japan.
Case Rep Otolaryngol. 2020 Sep 30;2020:8897868. doi: 10.1155/2020/8897868. eCollection 2020.
Primary solitary sphenoid sinus mucocele is rare, generally presenting with headaches or eye symptoms at the anatomical site. We report the case of a 39-year-old woman incidentally diagnosed with sphenoid sinus mucocele during a complete medical checkup. Imaging revealed that the cystic wall had developed from the rear sphenoid sinus and had spread expansively to diminish the clivus; however, no symptoms were reported, and the patient was managed with close observation. During the follow-up period, diplopia developed suddenly due to isolated left-sided abducens nerve paralysis. An endoscopic endonasal approach was used to open the frontal cystic wall, and fascia lata and fat were used for cranial base reinforcement to avoid future cerebrospinal fluid leakage, resulting in improvement during the early stages of follow-up. Treatment options for sphenoid sinus mucoceles include close observation or surgery. In our case, we chose surgery because of an acute symptomatic manifestation during observation.
原发性孤立性蝶窦黏液囊肿罕见,通常在解剖部位出现头痛或眼部症状。我们报告了一例39岁女性在全面体检时偶然诊断为蝶窦黏液囊肿的病例。影像学检查显示,囊肿壁由后蝶窦发展而来,并呈膨胀性扩展,致使斜坡骨质吸收;然而,患者并无症状报告,遂对其进行密切观察。在随访期间,患者突然因孤立性左侧展神经麻痹出现复视。采用鼻内镜经鼻入路打开额部囊肿壁,并使用阔筋膜和脂肪进行颅底加固,以避免未来脑脊液漏,在随访早期病情有所改善。蝶窦黏液囊肿的治疗选择包括密切观察或手术。在我们的病例中,由于观察期间出现急性症状表现,我们选择了手术治疗。