Bauman N M, Burke D K, Smith R J
Department of Otolaryngology-Head and Neck Surgery, University of Iowa College of Medicine, Iowa City 52242, USA.
Otolaryngol Head Neck Surg. 1997 Jul;117(1):99-110. doi: 10.1016/S0194-59989770215-8.
To assess the response of massive, life-threatening, or function-impairing hemangiomas in pediatric patients receiving daily alpha(2a)-interferon subcutaneously.
The effect of 3 or more months of subcutaneous alpha(2a)-interferon (3 mU/m2) was prospectively evaluated in 10 patients with hemangiomas necessitating medical intervention. Hemangioma characteristics and extent were initially assessed by radiographic imaging in all but one patient. alpha(2a)-Interferon tolerance was monitored, and reduction in hemangioma size was recorded as marked (>50%), moderate (25% to 50%), or minimal (<25%).
Hemangiomas were apparent at birth in 8 of 10 patients, and alpha(2a)-interferon was initiated at a median age of 4.5 months. Symptoms necessitating therapeutic intervention included congestive heart failure, airway obstruction, dysphagia, infection, failure to thrive, external auditory canal occlusion, visual axis impairment, and severe facial deformity. Four patients received treatment before referral that included systemic steroids (n = 2), intralesional steroids (n = 1), or surgical/laser excision (n = 2). alpha(2a)-Interferon therapy was well tolerated. Most patients had a temporary elevation in body temperature during the first month of therapy. One patient with anorexia required nasogastric feedings and a temporary reduction in her alpha(2a)-interferon dose. An additional patient with irritability was withdrawn from the study at his parents' request even though this symptom persisted after drug cessation. Hemangioma response to alpha(2a)-interferon was marked in six patients, moderate in two, and minimal in one whose lesion had features suggestive of a vascular malformation. Early signs of involution were usually evident within 6 weeks and often heralded by cutaneous blanching. alpha(2a)-interferon therapy was concluded in four patients after a mean duration of 20 months.
Daily subcutaneous alpha(2a)-interferon is well tolerated in pediatric patients and appears effective in hastening involution of symptomatic hemangiomas. A significant response is unlikely in lesions with features suggestive of a vascular malformation.
评估皮下每日注射α(2a)干扰素对患有大面积、危及生命或功能受损血管瘤的儿科患者的疗效。
对10例需要药物干预的血管瘤患者进行了前瞻性评估,观察皮下注射α(2a)干扰素(3百万单位/平方米)3个月或更长时间的效果。除1例患者外,所有患者最初均通过影像学检查评估血管瘤的特征和范围。监测α(2a)干扰素的耐受性,并将血管瘤大小的缩小记录为显著(>50%)、中度(25%至50%)或轻度(<25%)。
10例患者中有8例在出生时即有明显血管瘤,开始使用α(2a)干扰素的中位年龄为4.5个月。需要治疗干预的症状包括充血性心力衰竭、气道阻塞、吞咽困难、感染、生长发育迟缓、外耳道阻塞、视轴受损和严重面部畸形。4例患者在转诊前接受过治疗,包括全身用类固醇(n = 2)、瘤内注射类固醇(n = 1)或手术/激光切除(n = 2)。α(2a)干扰素治疗耐受性良好。大多数患者在治疗的第一个月体温暂时升高。1例厌食患者需要鼻饲,并暂时减少其α(2a)干扰素剂量。另1例烦躁不安的患者应其父母要求退出研究,尽管停药后该症状仍持续存在。6例患者的血管瘤对α(2a)干扰素反应显著,2例中度反应,1例轻度反应,其病变具有血管畸形特征。消退的早期迹象通常在6周内明显,常以皮肤变白为先兆。4例患者平均治疗20个月后结束α(2a)干扰素治疗。
每日皮下注射α(2a)干扰素在儿科患者中耐受性良好,似乎对加速有症状血管瘤的消退有效。具有血管畸形特征的病变不太可能有显著反应。