中华皮肤科杂志 ›› 2011, Vol. 44 ›› Issue (9): 615-617.

• 论著 • 上一篇    下一篇

母女同患Olmsted综合征

陈龙1,贺美林1,覃莉2,孔庆云3,4   

  1. 1. 武汉市一医院皮肤科
    2. 武汉市第一医院皮肤科
    3. 武汉市一医院
    4.
  • 收稿日期:2010-11-30 修回日期:2011-04-14 出版日期:2011-09-15 发布日期:2011-08-31
  • 通讯作者: 陈龙 E-mail:chenlong71@hotmail.com

Olmsted syndrome in a baby girl and her mother

  • Received:2010-11-30 Revised:2011-04-14 Online:2011-09-15 Published:2011-08-31

摘要:

例1女,2月龄,全身起角化性斑块近2个月。体检:眶周、口周、外阴、肛周可见片状境界较清楚角化性暗红色斑块,厚层鳞屑,局部见轻度浸渍,双足及双手掌可见黄色厚痂、皲裂。例2女,例1的母亲,24岁,口周、肛周角化性斑块,先天性普秃,双手足指(趾)残毁至指(趾)末端,残毁端见大量黄色肥厚性、角化性痂屑。例1臀部皮损组织病理检查:表皮呈银屑病样增生,真皮乳头及浅层血管周围可见不等量炎性细胞浸润。免疫组化:AE1在表皮棘层颗粒层染色阳性,CK10在棘层上部和颗粒层阳性。电镜检查:细胞间距增大,张力丝减少。诊断:母女同患Olmsted综合征。

关键词: 掌跖角皮症

Abstract:

A 2-month-old baby girl developed universal keratotic plaques soon after birth. Physical examination revealed well-defined, dark erythematous, keratotic plaques with thick scales and mild infiltration at the periorbital, perioral, perianal and vulvar regions, as well as deep fissures of both hands and feet covered with thick yellowish crusts. Another case was a 24-year-old female, the mother of the baby, who presented with hyperkeratotic plaques at perioral and perianal regions, congenital alopecia universalis, mutilation of fingers and toes with massive thick keratotic yellow crusts and scales. Histopathology of skin lesions from the gluteal region of the baby showed psoriasiform hyperplasia of the epidermis, slight inflammatory infiltration of dermal papillae and superficial dermal perivascular regions. Immunohistochemistry demonstrated the positive staining for acidic keratin (AE1) in the prickle cell layer and granular layer and for CK10 in the upper prickle cell layer and granular layer. Electron microscopy showed increased cell space and decreased tonofilament. Both the baby girl and her mother were diagnosed with Olmsted syndrome.

Key words: Palmoplantar keratoderma