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一例色素失禁症伴多器官异常。

A case of incontinentia pigmenti associated with multiorgan abnormalities.

作者信息

Chung Woon-Kyong, Lee Deok-Woo, Chang Sung-Eun, Lee Mi-Woo, Choi Jee-Ho, Moon Kee-Chan

机构信息

Department of Dermatology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.

出版信息

Ann Dermatol. 2009 Feb;21(1):56-9. doi: 10.5021/ad.2009.21.1.56. Epub 2009 Feb 28.

Abstract

Incontinentia pigmenti is a systemic disorder affecting the skin, teeth, eyes, nervous tissue, hair, nails, musculoskeletal system, and heart. We describe an 11-month-old girl with incontinentia pigmenti associated with a ventricular septal defect, left hemiatrophy, hemangiomas, an abnormal labial frenum, and spastic cerebral palsy manifested as left hemiplegia and developmental delay. We believe this patient illustrates that incontinentia pigmenti is a systemic disorder necessitating a multidisciplinary approach to management.

摘要

色素失禁症是一种影响皮肤、牙齿、眼睛、神经组织、毛发、指甲、肌肉骨骼系统和心脏的全身性疾病。我们描述了一名11个月大的患有色素失禁症的女孩,她还伴有室间隔缺损、左侧半身萎缩、血管瘤、唇系带异常以及表现为左侧偏瘫和发育迟缓的痉挛性脑瘫。我们认为该患者表明色素失禁症是一种全身性疾病,需要多学科方法进行管理。

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引用本文的文献

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Incontinentia Pigmenti: A Case Report of a Complex Systemic Disease.色素失禁症:一例复杂系统性疾病的病例报告
Open Access Maced J Med Sci. 2017 Jul 23;5(4):501-505. doi: 10.3889/oamjms.2017.128. eCollection 2017 Jul 25.

本文引用的文献

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Incontinentia pigmenti in male patients.男性患者的色素失禁症
J Am Acad Dermatol. 2006 Aug;55(2):251-5. doi: 10.1016/j.jaad.2005.12.015. Epub 2006 May 15.
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Clinical study of 40 cases of incontinentia pigmenti.40例色素失禁症的临床研究
Arch Dermatol. 2003 Sep;139(9):1163-70. doi: 10.1001/archderm.139.9.1163.
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Incontinentia pigmenti associated with bilateral cleft lip and palate.色素失禁症伴双侧唇腭裂。
Clin Exp Dermatol. 1991 Jan;16(1):49-50. doi: 10.1111/j.1365-2230.1991.tb00296.x.
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Trisomy 14 mosaicism in a 5-year-old boy.一名5岁男孩的14号染色体三体嵌合体。
Am J Med Genet. 1991 Jul 1;40(1):80-3. doi: 10.1002/ajmg.1320400116.

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