Beckerman R C, Taussig L M, Froede R C, Coulthard S W, Firor H, Tonkin I
Am J Dis Child. 1980 Feb;134(2):153-5. doi: 10.1001/archpedi.1980.02130140027008.
An 11-month-old infant had a history of dysphagia and continuous drooling without evidence for airway obstruction. A biopsy specimen of a neck mass on the left side adherent to the larynx and esophagus demonstrated pathologic features characteristic of a fibromuscular hamartoma. Upper airway obstruction subsequently ensued and the patient was managed for 16 months with a tracheostomy and feeding gastrostomy. Although posing an extremely difficult management problem, this benign tumor was surgically removed without damage to the larynx when the patient was 28 months old. The differential diagnosis of this unusual lesion must consider congenital fibromatosis and fetal rhabdomyoma.
一名11个月大的婴儿有吞咽困难和持续流口水的病史,无气道梗阻迹象。左侧颈部肿物的活检标本附着于喉和食管,显示出纤维肌性错构瘤的病理特征。随后出现上气道梗阻,患者通过气管造口术和胃造口术喂养管理了16个月。尽管这是一个极其棘手的管理问题,但当患者28个月大时,这个良性肿瘤被手术切除,未损伤喉部。这种不寻常病变的鉴别诊断必须考虑先天性纤维瘤病和胎儿横纹肌瘤。