Congenital laryngocele is an uncommon cause of neonatal stridor. There are only a few cases reported in the literature. The authors present a successfully treated case of an infant, whose life could only be saved by urgent tracheostomy. On the 5th postoperative day endoscopic excision and marsupialization provided patent airway. The patient could be decannulated. During follow-up no recurrence was observed.
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http://dx.doi.org/10.1186/s40463-020-00430-9 | DOI Listing |
Cureus
November 2024
Otolaryngology - Head and Neck Surgery, Hospital Tuanku Ampuan Najihah, Kuala Pilah, MYS.
Laryngocele is a rare condition marked by an abnormal enlargement of the air-filled saccule of the laryngeal ventricle. This case report showcases a distinctive presentation of external laryngocele to assist clinicians in its diagnosis and management. A 43-year-old male, with a 20-year history of painless swelling on the right side of his neck, likened to the size of an orange, presented with a recent increment in size.
View Article and Find Full Text PDFIndian J Otolaryngol Head Neck Surg
August 2024
Department of ENT, Mahatma Gandhi University of Medical Sciences and Technology (MGUMST), Sitapura, Jaipur, Rajasthan 302022 India.
Ear Nose Throat J
June 2024
Department of Otorhinolaryngology, Al Mouwasat University Hospital, Faculty of Medicine, Damascus University, Damascus, Syria.
Vestn Otorinolaringol
May 2024
Kuban State Medical University, Krasnodar, Russia.
Laryngeal air cyst (laryngocele) is a rare disease that is an abnormal cystic expansion of the deep structures of the laryngeal ventricle. They can be accompanied by serious complaints, such as shortness of breath, difficulty breathing during exercise, as well as at rest with large cysts. Computed tomography is the most effective method for determining the type, localization and degree of laryngocele.
View Article and Find Full Text PDFEur Arch Otorhinolaryngol
August 2024
Faculty of Medicine of Sfax, Otolaryngology- Head and Neck Surgery Department and Research Laboratory LR23ES01, Habib Bourguiba Hospital, 3029, Sfax, Tunisia.
Introduction: We describe a first case of human congenital crico-thyroid dysplasia associated to a right sided aortic arch and an aberrant subclavian artery.
Case Presentation: Our patient presented with a two-weeks history of acute dyspnea, and reported hoarseness since his childhood. An urgent tracheotomy was performed, followed by direct laryngoscopy.
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