Cen Qingqing,Chen Xuanfeng,Lin Xiaoxi,et al.Advances in the diagnosis and treatment of midline facial capillary malformations in infants[J].Journal of Clinical Pediatric Surgery,,18():650-654.[doi:10.3969/j.issn.1671-6353.2019.08.007]
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Advances in the diagnosis and treatment of midline facial capillary malformations in infants

References:

1 Rozas-Munoz E,Frieden IJ,Roe E,et al.Vascular stains:proposal for a clinical classification to improve diagnosis and management[J].Pediatr Dermatol,2016,33(6):570-584.DOI:10.1111/pde.12939.
2 Dasgupta R,Fishman SJ.ISSVA classification[J].SeminPediatr Surg,2014,23(4):158-161.DOI:10.1053/j.sempedsurg.2014.06.016.
3 林晓曦.血管瘤和脉管畸形的新分类及诊疗进展(2015-2016年)[J].中国美容整形外科杂志,2016,27(6):321-325.DOI:10.3969/j.issn.1673-7040.2016.06.001.Lin XX.Advances in new classification,diagnosis and treatment of hemangiomas and vascular malformations(2015-2016)[J].Chin J Aesth Plast Surg,2016,27(6):321-325.DOI:10.3969/j.issn.1673-7040.2016.06.001.
4 Juern AM,Glick ZR,Drolet BA,et al.Nevus simplex:A reconsideration of nomenclature,sites of involvement,and disease associations[J].J Am Acad Dermatol,2010,63(5):805-814.DOI:10.1016/j.jaad.2009.08.066.
5 Shih IH,Jy L,Chen CH,et al.A birthmark survey in 500 newborns:clinicalobservation in two northern Taiwan medical center nurseries[J].Chang Gung Med J,2007,30(3):220-225.
6 Jacobs AH,Walton RG.The incidence of birthmarks in the neonate[J].Pediatrics,1976,58(2):218-222.
7 Van Drooge AM,Beek JF,Van Der Veen JP,et al.Hypertrophy in port-wine stains:prevalence and patient characteristics in a large patientcohort[J].J Am Acad Dermatol,2012,67(6):1214-1219.DOI:10.1016/j.jaad.2012.05.027.
8 王璐颖,霍然.Sturge-Weber综合征特点及诊断治疗研究进展[J].中国美容整形外科杂志,2016,27(6):329-333.DOI:10.3969/j.issn.1673-7040.2016.06.003.Wang LY,Huo R.Research advance of the characteristics,diagnosis and treatment of Sturge-Weber syndrome[J].Chin J Aesth Plastic Surg,2016,27(6):329-333.DOI:10.3969/j.issn.1673-7040.2016.06.003.
9 Comi AM.Sturge-Weber syndrome[J].Handb Clin Neurol,2015,132:157-168.DOI:10.1016/B978-0-444-62702-5.00011-1.
10 Dorairaj S,Ritch R.Eneephalotrigeminal angiomatosis(stu-rge-weber syndrome,klippel-lrenaunay-weber syndrome):a review[J].Asia Pac J Ophthalmol(Phila),2012,1(4):226-234.
11 Abdolrahimzadeh S,Scavella V,Felli LA,et al.Ophthalmic alterations in the Sturge-Weber syndrome,Klippel-Trenaunay syndrome,and the phakomatosis pigmentovascularis:an Independent group of conditions?[J].Biomed Res Int,2015,2015:786591.DOI:10.1155/2015/786519.
12 陈晓东,陈辉,马刚,等.新生儿红斑的自然病程及其与葡萄酒色斑的鉴别研究诊断[J].组织工程与重建外科杂志,2012,8(2):84-87.DOI:10.3969/j.issn.1673-0364.2012.02.006.Chen XD,Chen H,Ma G.,et al.The natural course of salmon patch and the identification between salmon patch and port wine stain[J].Journal of Tissue Engineering and Reconstructive Surgery,2012,08(2):84-87.DOI:10.3969/j.issn.1673-0364.2012.02.006.
13 Happle R.What is a capillary malformation?[J].J Am Acad Dermatol,2008,59(6):1077-1079.DOI:10.1016/j.jaad.2008.07.035.
14 Traupe H.A rose is a rose:naevoid manifestations blur the boundary between naevus and classical gene defect in focal dermal hypoplasia[J].Br J Dermatol,2019,180(3):461-462.DOI:10.1111/bjd.17185.
15 Happle R.Capillary malformations:a classification using specific names for specific skindisorders[J].J Eur Acad Dermatol Venereol,2015,29(12):2295-2305.
16 Piram M,Lorette G,Sirinelli D,et al.Sturge-Weber syndrome in patients with facial port-wine stain[J].Pediatr Dermatol,2012,29(1):32-37.
17 Mehta M,Salas AH,Fay A.Trigeminal dermatome distribution in patientswith glaucoma and facial port wine stain[J].Dermatology,2009,219(3):219-224.
18 Shirley MD,Tang H,Gallione CJ,et al.Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ[J].N Engl J Med,2013,368(21):1971-1979.
19 Waelchli R,Aylett SE,Robinson K,et al.New vascular classification of port-wine stains:improving prediction of Sturge-Weber risk[J].Br J Dermatol,2014,171(4):861-867.DOI:10.1111/bjd.13203.
20 Waner M,North PE,Scherer KA,et al.The nonrandom distribution of facial hemangiomas[J].Arch Dermatol,2003,139(7):869-875.DOI:10.1001/archderm.139.7.869.
21 Haggstrom AN,Lammer EJ,Schneider RA,et al.Patterns of infantilehemangiomas:new clues to hemangioma pathogenesis and embryonic facialdevelopment[J].Pediatrics,2006,117(3):698-703.DOI:10.1542/peds.2005-1092.
22 Dutkiewicz AS,Ezzedine K,Mazereeuw-Hautier J,et al.A prospective study of risk for Sturge-Weber syndrome in children with upper facial port-wine stain[J].J Am Acad Dermatol,2015,72(3):473-480.
23 Cai R,Liu F,Cen Q,et al.Capillary malformation in the midline of the face:Salmon patchor port-wine stain?[J].J Dermatol,2018,45(11):317-319.DOI:10.1111/1346-8138.14345.
24 Griffiths PD.Sturge-Weber syndrome revisited:the role of neuroradiology[J].Neuropediatrics,1996,27(6):284-294.DOI:10.1055/s-2007-973796.
25 Bar C,Pedespan JM,Boccara O,et al.Early magnetic resonance imaging to detect presymptomatic leptomeningeal angioma in children with suspected Sturge-Weber syndrome[J].Dev Med Child Neurol,2019,18(8):509-516.
26 Andica C,Hagiwara A,Hori M,et al.Aberrant myelination in patients with Sturge-Weber syndrome analyzed using synthetic quantitative magnetic resonance imaging[J].Neuroradiology,2019,14(2):409-415.DOI:10.1007/s00234-019-02250-9.
27 Adams ME,Aylett SE,Squier W,et al.A spectrum of unusual neuroimaging findingsin patients with suspected Sturge-Weber syndrome[J].AJNR Am J Neuroradiol,2009,30(2):276-281.DOI:10.3174/ajnr.A1350.
28 Piram M,Lorette G,Sirinelli DA,et al.Sturge-Weber syndrome in patients with facial Port-Wine stain[J].Pediatr Dermatol,2012,29(1):32-37.DOI:10.1111/j.1525-1470.2011.01485.x.
29 Zallmann M,Leventer RJ,Mackay MT,et al.Screening for Sturge-Weber syndrome:astate-of-the-art review[J].Pediatr Dermatol,2018,35(1):30-42.
30 吴越,虞茹静,林晓曦,等.葡萄酒色斑患者Sturge-Weber综合征继发性青光眼的临床特征分析[J].中华眼科杂志,2017,53(10):753-757.DOI:10.3760/cma.j.issn.0412-4081.2017.10.007.Wu Y,Yu RJ,Lin XX,et al. Sturge-Weber syndrome in port-wine stain patients:a retrospective study on the clinical features and screening strategy[J].Chin J Ophthalmol,2017,53(10):753-757.DOI:10.3760/cma.j.issn.0412-4081.2017.10.007.

Memo

收稿日期:2019-05-27。
基金项目:院内临床助力计划(编号:JYLJ001)
通讯作者:林晓曦,Email:linxiaoxi@126.com;蔡韧,Email:drrencai@gmail.com

Last Update: 1900-01-01