CUTANEOUS GRANULOMATOUS LESIONS IN PATIENTS WITH ATAXIA-TELANGIECTASIA

被引:50
作者
PALLER, AS
MASSEY, RB
CURTIS, MA
PELACHYK, JM
DOMBROWSKI, HC
LEICKLY, FE
SWIFT, M
机构
[1] NORTHWESTERN UNIV, SCH MED, DEPT PEDIAT, CHICAGO, IL 60611 USA
[2] NORTHWESTERN UNIV, SCH MED, DEPT DERMATOL, CHICAGO, IL 60611 USA
[3] HOSP SICK CHILDREN, DEPT DERMATOL, TORONTO M5G 1X8, ONTARIO, CANADA
[4] HENRY FORD HOSP, DEPT DERMATOL, DETROIT, MI 48202 USA
[5] HENRY FORD HOSP, DEPT PEDIAT ALLERGY IMMUNOL, DETROIT, MI 48202 USA
[6] UNIV N CAROLINA, BIOL SCI RES CTR, DEPT MED, CHAPEL HILL, NC 27514 USA
[7] UNIV N CAROLINA, DEPT EPIDEMIOL, CHAPEL HILL, NC 27514 USA
关键词
D O I
10.1016/S0022-3476(05)83043-4
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
Ataxia-telangiectasia is a genetic syndrome with progressive cerebellar ataxia, oculocutaneous telangiectasias and other skin manifestations, variable immune system defects, chronic progressive sinopulmonary disease, and a high incidence of cancer. Cutaneous granulomas developed and persisted in eight patients with ataxia-telangiectasia, despite treatment with intravenously administered immune globulin, topical antibiotic therapy, and potent topical corticosteroid therapy. We were unable to identify an infectious agent; the granulomas may develop in an attempt to localize antigen in the presence of a dysfunctional immune system.
引用
收藏
页码:917 / 922
页数:6
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