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男性色素失禁症1例

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摘要 1临床资料 患者男,10个月,因＂躯干四肢褐色沉着斑6个月＂于2010年5月15日到我科就诊。患者于出生后9d发现躯干四肢在红斑基础上出现条带状及网状绿豆至黄豆大小不等水疱,疱液澄清,不易破溃,黏膜无异常。实验室检查：血常规示白细胞总数为30.97×10^9/L（15.0-20.0×10^9/L）,
作者 郭波 宋为民 艾俊俊
机构地区 浙江中医药大学 浙江中医药大学附属杭州第三人民医院 安徽医科大学杭州临床学院
出处 《中国中西医结合皮肤性病学杂志》 CAS 2011年第1期48-49,共2页 Chinese Journal of Dermatovenereology of Integrated Traditional and Western Medicine
关键词 男性 婴儿 色素失禁症
分类号 R758.5 [医药卫生—皮肤病学与性病学]
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参考文献6

  • 1Mini(c) S,Novotnyt GE,Medenica L,et al.Two male patients with incontinentia pigmenti[J].Vojnosanit Pregl,2010,67:183-186.
  • 2Berlin AL,Paller AS,Chan LS.Incontinentia pigmenti:a review and update on the molecular basis of pathophysiology[J].J Am Acad Dermatol,2002,47:169-187.
  • 3Smahi A,Courtois G,Vabres P,et al.Genomic rearrangement in NEM0 impairs NF-kappaB activation and is a cause of incontinentia pigmenti.The International Incontinentia Pigmenti (IP)Consortium[J].Nature,2000,405:466-472.
  • 4周顺铭,张学军,杨森.色素失禁症的分子遗传学研究进展[J].国外医学（皮肤性病学分册）,2005,31(4):247-249. 被引量：4
  • 5Aradhya S,Courtois G,Rajkovic A,et al.Atypical forms of incontinentia pigrnenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma)[J].Am J Hum Genet,2001,68:765-771.
  • 6Arenas-sordo Mde L,Vallejo-Vega B,Hernández-Zamora E,et al.Incontinentia pigmenti (IP2):Familiar case report with affected men[J].Med Oral Patol Oral Cir Bucal,2005,10:E122-129.

二级参考文献23

  • 1Jean-Baptiste S, OToole EA, Chen M, et al. Expression of eotaxin,an eosinophil-selective chemokine, parallels eosinophil accumulation in the veslculobullous stage of incontinentia pigmenti. Clin Exp Immunol,2002,127:470-478.
  • 2Berlin AL, Paller AS, Chan LS. Incontinentia pigmenti: a review and update on the molecular basis of pathophysiology. J Am Acad Dermatol, 2002,47:169-187.
  • 3Topham E J, Simpson Dent SL, Child FJ. Case 1. Incontinentia pigmenti. Clin Exp Dermatol, 2003, 28:103-104.
  • 4Scardamaglia L, Howard A, Sinclair R. Twenty-nail dystrophy in a girl with incontinentia pigmenti. Australas J Dermatol, 2003, 44:71-73.
  • 5Mayer E J, Shuttleworth GN, Greenhalgh KL, et al. Novel corneal features in two males with incontinentia pigmenti. Br J Ophthalmol,2003, 87:554-556.
  • 6Cates CA, Dandekar SS, Flanagan DW, et al. Retinopathy of incontinentia pigmenti: a case report with thirteen years follow-up. Ophthalmic Genet, 2003, 24:247-252.
  • 7Porksen G, Pfeiffer C, Hahn G, et al. Neonatal seizures in two sisters with incontinentia pigmenti. Neuropediatrics, 2004, 35:139-142.
  • 8I Jewett T, Hart PS, Rao PN, et al. A case revisited: recent presentation of incontinentia pigmenti in association with a previously reported X;autosome translocation. Am J Med Genet, 1997, 69:96-97.
  • 9Smahi A, Hyden-Granskog C, Peterlin B, et al. The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28. Hum Mol Genet, 1994, 3:273-278.
  • 10Smahi A, Courtois G, Vabres P, et al. Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.Nature, 2000,405:466-472.

共引文献3

中国中西医结合皮肤性病学杂志
2011年 第1期

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