Yokoyama Nayu, Komori Manabu
Department of Otolaryngology, St. Marianna University School of Medicine, Kawasaki, JPN.
Cureus. 2025 May 27;17(5):e84878. doi: 10.7759/cureus.84878. eCollection 2025 May.
Pyriform sinus cysts are rare congenital anomalies originating from the third or fourth branchial pouch that can cause neonatal airway obstruction. We report the case of a male neonate born at 38 weeks of gestation who developed respiratory distress at birth. Physical exam revealed subcostal retractions and nasal flaring, but no stridor. Laryngoscopy on day 4 demonstrated a bulging posterior pharyngeal wall, and computed tomography (CT) identified an air-filled cyst extending into the left neck, suggestive of a pyriform sinus cyst. Ultrasound (US)-guided aspiration of 7 mL of fluid temporarily relieved symptoms; however, recurrence necessitated surgical excision on the seventh day of life. The cyst and two fibrous cords were removed. Histology analysis confirmed infection with chronic inflammation and granulation tissue. The patient developed transient left vocal cord paralysis, which resolved within three months. Follow-up magnetic resonance imaging (MRI) showed no recurrence. This case highlights the importance of early diagnosis and surgical intervention to prevent airway obstruction, while emphasizing the roles of imaging, nerve preservation, and postoperative monitoring. Further research into minimally invasive techniques and prenatal diagnosis is warranted.
梨状窦囊肿是一种罕见的先天性异常,起源于第三或第四鳃囊,可导致新生儿气道阻塞。我们报告一例妊娠38周出生的男婴,出生时出现呼吸窘迫。体格检查发现肋下凹陷和鼻翼扇动,但无喘鸣。出生后第4天行喉镜检查显示咽后壁膨出,计算机断层扫描(CT)发现一个充满气体的囊肿延伸至左颈部,提示梨状窦囊肿。超声(US)引导下抽出7 mL液体暂时缓解了症状;然而,复发后在出生后第7天需要进行手术切除。囊肿和两条纤维索被切除。组织学分析证实有慢性炎症和肉芽组织感染。患者出现短暂性左侧声带麻痹,在3个月内恢复。随访磁共振成像(MRI)显示无复发。该病例强调了早期诊断和手术干预以预防气道阻塞的重要性,同时强调了影像学、神经保护和术后监测的作用。有必要进一步研究微创技术和产前诊断。