Lupus erythematosus-like lesions in a carrier of X-linked chronic granulomatous disease

被引:20
作者
Córdoba-Guijarro, S
Feal, C
Daudén, E
Fraga, J
García-Díez, A
机构
[1] Hosp Univ Princesa, Dept Dermatol, Madrid 28006, Spain
[2] Hosp Univ Princesa, Dept Pathol, Madrid 28006, Spain
关键词
lupus erythematosus; chronic granulomatous disease; immunodeficiency;
D O I
10.1046/j.1468-3083.2000.00113.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Chronic granulomatous disease (CGD) is an inherited immunodeficiency disease. Carrier status of CGD has been reported in association with lupus erythematosus-type lesions. A 35-year-old woman, mother of a child with X-linked CGD presented an 8-year history of erythematous plaques with an arciform pattern on the upper trunk, back and arms. The nitroblue tetrazolium test revealed the carrier status of the patient. Haematological, biochemical and immunological tests (including ANA, DNA, SSA-Ro, SSB-La, RNP, SM and Jol antibodies) were normal or negative except for a polyclonal hypergammaglobulinaemia with high serum IgA. Histological examination showed a papillary and perifollicular lymphohistiocytic infiltrate. Direct immunofluorescence was negative. We report a female carrier of X-linked CGD who developed clinical subacute lupus erythematosus-like lesions. We review the literature and discuss the pathogenetic mechanisms involved in the condition.
引用
收藏
页码:409 / 411
页数:3
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