[1]王娈,崔丽霞,刘鹏月,等.先天性毛细血管扩张性大理石样皮肤1例[J].中国皮肤性病学杂志,2019,(06):701-703.[doi:10.13735/j.cjdv.1001-7089.201809150]
 WANG Luan,CUI Lixia,LIU Pengyue,et al.A Case of Cutis Marmorata Telangiectatica Congenita[J].The Chinese Journal of Dermatovenereology,2019,(06):701-703.[doi:10.13735/j.cjdv.1001-7089.201809150]
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先天性毛细血管扩张性大理石样皮肤1例
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《中国皮肤性病学杂志》[ISSN:1001-7089/CN:61-1197/R]

卷:
期数:
2019年06期
页码:
701-703
栏目:
病例报告
出版日期:
2019-05-16

文章信息/Info

Title:
A Case of Cutis Marmorata Telangiectatica Congenita
文章编号:
1001-7089(2019)06-0701-03
作者:
王娈1崔丽霞2刘鹏月1韩秀萍1
1.中国医科大学附属盛京医院皮肤科,辽宁 沈阳 110004; 2.海南医学院第二附属医院皮肤科,海南 海口 570100
Author(s):
WANG Luan1CUI Lixia2LIU Pengyue1HAN Xiuping1
(1.Department of Dermatology,Shengjing Hospital of China Medical University,Shenyang 110004,China; 2.Department of Dermatology,the Second Affiliated Hospital of Hainan Medical University,Haikou 570100,China)
关键词:
先天性毛细血管扩张性大理石样皮肤
Keywords:
Cutis marmorata telangiectatica congenita
分类号:
R 758.57
DOI:
10.13735/j.cjdv.1001-7089.201809150
文献标志码:
B
摘要:
患儿男,生后1 d,自出生时发现全身皮肤呈紫红色网状花纹样改变。内科系统检查未见明显异常。皮肤科情况:面部见少量淡红色网状斑,躯干下部、四肢广泛分布紫红色血管扩张,呈网状及树枝状分布,部分皮疹处皮肤及皮下组织萎缩,双下肢粗细不同。诊断:先天性毛细血管扩张性大理石样皮肤。随访3个月,患儿皮疹颜色较生时浅淡,仍有双下肢粗细差异与局部皮肤及皮下组织萎缩。
Abstract:
A one-day-old boy presented with a red-purple reticular pattern from birth.No obvious abnormalities were found in the medical examination.Dermatologic examination revealed reddish reticular macules on the face,red-purple reticular vasodilatation on the limbs and lower part of the trunk.The skin and subcutaneous tissue of some rashes were atrophied and the thickness of the legs was different.He was diagnosed as cutis marmorata telangiectatica congenita.During the follow-up of three months,the color of the rashes became lighter.Still,there was difference in the thickness of legs.Atrophy of the local skin and subcutaneous tissue still existed.

参考文献/References:


[1] Deshpande AJ.Cutis marmorata telangiectatica congenita successfully treated with intense pulsed light therapy:A case report[J].Cosmet Laser Ther,2018,20(3):145-147.
[2] Wollina U,França K,Lotti T,et al.Van Lohuizen syndrome-a case report with a diagnostic delay of four years[J].Open Access Maced J Med Sci,2018,6(1):74-75.
[3] Happle R.Capillary malformations:a classification using specific names for specific skin disorders[J].Eur Acad Dermatol Venereol,2015,29(12):2295-2305.
[4] Matic A,Pricic S,Matic M,et al.Cutis marmorata telangiectatica congenita in a preterm newborn:case report and literature review[J].Iran Red Crescent Med,2012,14(9):578-583.
[5] Ponnurangam VN,Paramasivam V.Cutis marmorata telangiectatica congenita[J].Indian Dermatol Online,2014,5(1):80-82.
[6] Kienast AK,Hoeger PH.Cutis marmorata telangiectatica congenita:a prospective study of 27 cases and review of the literature with proposal of diagnostic criteria[J].Clin Exp Dermatol,2009,34(3):319-323.
[7] Garzon MC,Schweiger E.Cutis marmorata telangiectatica congenita[J].Semin Cutan Med Surg,2004,23(2):99-106.
[8] Levy R,Lam JM.Cutis marmorata telangiectatica congenita:a mimicker of a common disorder[J].Can Med Assoc J,2011,183(4):249-251.
[9] Ilhan O,Ozer EA,Ozdemir SA,et al.Congenital cutis marmorata telangiectatica and syndactyly in a preterm:case report[J].Arch Argent Pediatr,2016,114(2):111-113.
[10] 李波,谭军.先天性面部毛细血管扩张大理石样皮肤及其治疗一例[J].中国美容医学,2011,20(8):1278.

备注/Memo

备注/Memo:
[基金项目] 辽宁省重点研发计划项目(2017225026); 沈阳市科学与技术项目(17-230-9-25)
[作者单位] 1.中国医科大学附属盛京医院皮肤科,辽宁 沈阳 110004; 2.海南医学院第二附属医院皮肤科,海南 海口 570100
[通讯作者] 韩秀萍,E-mail:hanxiuping66@126.com
更新日期/Last Update: 2019-05-16