未经授权:先天性喉网是一种罕见的疾病,可引起喘鸣,呼吸困难,声音嘶哑,和其他症状。患有这种疾病的儿童通常患有喘鸣,虚弱的哭泣,出生时声音嘶哑,但是这些症状也可能在白天发生,周,月,甚至出生后几年。呼吸道感染会明显加重这些表现,对症治疗后恢复缓慢。颈部CT和喉镜检查可以检测和诊断这种疾病。重要的是,可以在出生后复发性喘鸣和持续声音嘶哑的婴儿中考虑和检查该疾病。
未经评估:我们报告了一个23个月大的男孩,他出生后因喘鸣和声音嘶哑入院。结合喉镜检查的结果,他被诊断出患有先天性喉网,并通过支气管镜进行二氧化碳(CO2)激光治疗和冷冻治疗。预后良好。
未经授权:先天性喉网是一种罕见但具有挑战性的喉部病变。对于出生后复发性喘鸣和持续性声音嘶哑的婴儿,可以考虑和检查该疾病非常重要。诊断后应根据喉网的分类和儿童症状的严重程度确定治疗策略。
UNASSIGNED: Congenital laryngeal web is a rare disease that can cause
stridor, dyspnea, hoarseness, and other symptoms. Children with this disease generally have
stridor, weak crying, and hoarseness at birth, but these symptoms can also occur during the days, weeks, months, and even years after birth. Respiratory tract infection will obviously aggravate these manifestations, and recovery is slow after symptomatic treatment. Neck CT and laryngoscopy can detect and diagnose this disease. It is important that the disease can be considered and examined in infants with recurrent
stridor and persistent hoarseness after birth.
UNASSIGNED: We report a 23-month-old boy who was admitted to hospital due to
stridor and hoarseness after birth. Combined with the results of laryngoscopy, he was diagnosed with congenital laryngeal web, and was treated with carbon dioxide (CO2) laser and cryotherapy by bronchoscope. The prognosis was good.
UNASSIGNED: Congenital laryngeal web is a rare but challenging laryngeal lesion. It is very important that the disease can be considered and examined for infants with recurrent
stridor and persistent hoarseness after birth. The treatment strategy after diagnosis should be determined according to the classification of laryngeal web and the severity of children\'s symptoms.