新生儿先天性双侧鼻泪管囊肿伴呼吸窘迫1例

IF 0.3 Q4 OTORHINOLARYNGOLOGY
Haruo Yoshida, Chiharu Kihara, Kyoko Kitaoka, Chisei Satoh, Y. Kumai
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引用次数: 0

摘要

摘要鼻泪管囊肿是一种罕见的泪囊囊肿合并症。我们描述了一个0天大的女婴新生儿呼吸窘迫综合征发展后立即出生的情况。鼻内窥镜和磁共振成像显示双侧下道NLD囊肿。急救时在右鼻腔内插入鼻咽导气管,有效改善了患者的呼吸状况。然而,她的呼吸状况在29日龄时迅速恶化。因此,在61日龄时进行了微清创辅助下的内镜有袋化手术。该手术不需要任何特殊技术,囊肿壁在全身麻醉下被充分切除。术后呼吸状况立即改善,无并发症或囊肿复发报告。先天性NLD囊肿引起的新生儿呼吸窘迫综合征可在眼周无异常表现,突出了将这种情况作为鉴别诊断的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital bilateral nasolacrimal duct cysts with respiratory distress in a newborn
Abstract Nasolacrimal duct (NLD) cysts are a rare comorbidity of dacryocystocele. We describe the case of a 0-day-old female infant with neonatal respiratory distress syndrome developing immediately after birth. Nasal endoscopy and magnetic resonance imaging revealed bilateral NLD cysts in the inferior meatus. A nasopharyngeal airway was inserted into the right nasal cavity as first aid, which effectively improved the patient’s respiratory condition. However, her respiratory condition deteriorated rapidly at 29 days of age. Hence, microdebrider-assisted endoscopic marsupialization was performed at 61 days of age. This procedure does not require any special techniques, and the cyst wall was adequately removed under general anesthesia. Her respiratory condition improved immediately postoperatively, and no complications or recurrence of the cyst have been reported to date. Neonatal respiratory distress syndrome due to congenital NLD cyst can present without abnormal findings around the eye, highlighting the importance of considering this condition as a differential diagnosis.
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