Patnaik Suprabha Kumari, Sondhi Vishal
Military Hospital, Pediatrics, Cantt, Saugor, Madhya Pradesh, 470001, India.
BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.11.2008.1214. Epub 2009 Apr 7.
Subglottic haemangiomas are benign vascular malformations presenting in early infancy with respiratory distress due to progressive airway obstruction. The lesion, after undergoing proliferation during the first few months, naturally involutes by an age of 2-3 years. Due to high incidence of mortality, therapy should be initiated immediately. Multiple therapeutic options, such as steroids, interferon, surgery and laser ablation, are available but the best treatment is controversial. This report describes an infant presenting with respiratory distress and cutaneous haemangioma who was detected to have airway obstructive haemangioma from the subglottis to the carina. Due to the massive size, surgical and laser ablation could not be exercised. Also, the infant showed no response to dexamethasone, prednisolone or interferon. Following failure of these modalities, the infant was successfully managed with concurrent administration of daily interferon and pulse methylprednisolone. The regime resulted in rapid shrinkage of the haemangioma and resolution of symptoms, with no recurrence up to 24 months of age.
声门下血管瘤是一种良性血管畸形,在婴儿早期出现,由于进行性气道阻塞而导致呼吸窘迫。该病变在最初几个月增殖后,在2至3岁时自然消退。由于死亡率高,应立即开始治疗。有多种治疗选择,如类固醇、干扰素、手术和激光消融,但最佳治疗方法存在争议。本报告描述了一名患有呼吸窘迫和皮肤血管瘤的婴儿,该婴儿被检测出从声门下到隆突存在气道阻塞性血管瘤。由于血管瘤体积巨大,无法进行手术和激光消融。此外,该婴儿对地塞米松、泼尼松龙或干扰素无反应。在这些治疗方法失败后,通过同时每日给予干扰素和脉冲甲基泼尼松龙,该婴儿成功得到治疗。该治疗方案导致血管瘤迅速缩小,症状缓解,至24个月龄时无复发。