Infantile haemangioma

被引:320
|
作者
Leaute-Labreze, Christine [1 ]
Harper, John I. [2 ,3 ]
Hoeger, Peter H. [4 ,5 ]
机构
[1] Pellegrin Childrens Hosp, Dept Dematol, F-33076 Bordeaux, France
[2] Inst Child Hlth, Dept Paediat Dermatol, London, England
[3] Great Ormond St Hosp Sick Children, London, England
[4] Catholic Childrens Hosp, Dept Paediat, Hamburg, Germany
[5] Catholic Childrens Hosp, Dept Paediat Dermatol, Hamburg, Germany
来源
LANCET | 2017年 / 390卷 / 10089期
关键词
PULSED DYE-LASER; ULCERATED HEMANGIOMAS; ORAL PROPRANOLOL; PHACE SYNDROME; CASE-SERIES; KAPOSIFORM HEMANGIOENDOTHELIOMA; CLINICAL CHARACTERISTICS; SUBTYPE CLASSIFICATION; GROWTH; INFANCY;
D O I
10.1016/S0140-6736(16)00645-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
With a prevalence of 4.5%, infantile haemangiomas are the most common benign tumours of infancy, arising in the first few weeks of life and exhibiting a characteristic sequence of growth and spontaneous involution. Most infantile haemangiomas do not require therapy. However, to identify at-risk haemangiomas, close follow-up is crucial in the first weeks of life; 80% of all haemangiomas reach their final size by 3 months of age. The main indications for treatment are life-threatening infantile haemangioma (causing heart failure or respiratory distress), tumours posing functional risks (eg, visual obstruction, amblyopia, or feeding difficulties), ulceration, and severe anatomic distortion, especially on the face. Oral propranolol is now the first-line treatment, which should be administered as early as possible to avoid potential complications. Haemangioma shrinkage is rapidly observed with oral propranolol, but a minimum of 6 months of therapy is recommended.
引用
收藏
页码:85 / 94
页数:10
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