Georgetown University School of Medicine, Washington DC.
University of California, San Francisco, California.
J Am Acad Dermatol. 2019 Feb;80(2):493-499. doi: 10.1016/j.jaad.2018.07.061. Epub 2018 Oct 5.
The proliferative phase of infantile hemangiomas (IHs) is usually complete by 9 months of life. Late growth beyond age 3 years is rarely reported.
To describe the demographic and clinic characteristics of a cohort of patients with late growth of IH, defined as growth in a patient >3 years of age.
A multicenter, retrospective cohort study.
In total, 59 patients, 85% of which were female, met the inclusion criteria. The mean first episode of late growth was 4.3 (range 3-8.5) years. Head and neck location (55/59; 93%) and presence of deep hemangioma (52/59; 88%) were common characteristics. Posterior fossa malformations, hemangiomas, arterial anomalies, cardiac defects, eye abnormalities (PHACE) syndrome was noted in 20 of 38 (53%) children with segmental facial IH. Systemic therapy (corticosteroid or β-blocker) was given during infancy in 58 of 59 (98%) and 24 of 59 (41%) received systemic therapy (β-blockers) for late IH growth.
The retrospective nature and ascertainment by investigator recall are limitations of the study.
Late IH growth can occur in children after 3 years of age. Risk factors include head and neck location, segmental morphology, and involvement of deep dermal/subcutaneous tissues.
婴儿血管瘤(IHs)的增殖期通常在 9 个月大时完成。3 岁以后的晚期生长很少有报道。
描述一组晚期 IH 生长患者的人口统计学和临床特征,定义为年龄>3 岁的患者生长。
多中心回顾性队列研究。
共有 59 名患者符合纳入标准,其中 85%为女性。晚期生长的首次发作平均为 4.3 岁(范围 3-8.5 岁)。头颈部位置(55/59;93%)和深部血管瘤存在(52/59;88%)是常见的特征。38 例节段性面部 IH 患儿中有 20 例(53%)存在后颅窝畸形、血管瘤、动脉异常、心脏缺损、眼部异常(PHACE)综合征。59 例患儿中有 58 例(98%)在婴儿期接受全身治疗(皮质类固醇或β受体阻滞剂),24 例(41%)接受全身治疗(β受体阻滞剂)治疗晚期 IH 生长。
研究的局限性在于回顾性性质和研究者回忆的确定。
3 岁以后的儿童可能会发生晚期 IH 生长。危险因素包括头颈部位置、节段性形态和深真皮/皮下组织受累。