原发性孤立性蝶窦黏液囊肿伴颅底广泛骨变薄所致展外神经麻痹。

IF 0.4 Q4 OTORHINOLARYNGOLOGY Case Reports in Otolaryngology Pub Date : 2020-09-30 eCollection Date: 2020-01-01 DOI:10.1155/2020/8897868
Shoji Naito, Hidenori Yokoi, Yuma Matsumoto, Michitsugu Kawada, Kohei Inomata, Masachika Fujiwara, Arisa Ohara, Koichiro Saito
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引用次数: 1

摘要

原发性孤立性蝶窦黏液囊肿是罕见的,通常在解剖部位表现为头痛或眼部症状。我们报告的情况下,39岁的妇女偶然诊断为蝶窦粘液囊肿在一个完整的医疗检查。影像学显示囊壁从后蝶窦开始发育,并扩张性扩散,使斜坡缩小;然而,未报告任何症状,并对患者进行了密切观察。随访期间,因孤立性左侧外展神经麻痹,突然出现复视。内镜下鼻内入路打开额囊壁,颅底阔筋膜和脂肪加固,避免脑脊液再次漏出,随访早期情况有所改善。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,我们选择手术是因为在观察期间出现了急性症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Abducens Nerve Paralysis Induced by a Primary Solitary Sphenoid Sinus Mucocele with Broad Osseous Thinning at the Cranial Base.

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.

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来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
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发文量
20
审稿时长
13 weeks
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