摘要
报告皮肤弹性过度伴细胞免疫缺陷1例。患儿女,13岁。出生后即有皮肤弹性过度,脓疱疮反复发作4年。实验室检查发现有缺铁性贫血,皮损组织病理检查无特异性,脓液细菌培养出金黄色葡萄球菌,淋巴细胞亚群检查示CD332%,CD427%,CD820%,CD4/CD81.35。先后给予免疫调节剂、系统及外用抗生素、抗贫血药等治疗。患儿细胞免疫缺陷得到纠正,深脓疱疮及缺铁性贫血治愈。
A case of cutis hyperelastica complicated by the abnormity in immunoassay is reported. The 13-year-old girl had cutis hyperelastica for 13 years, with ecthyma on the face and extremities for 4 years. The lab examination showed an iron deficiency anemia. S.aureus was detected from ecthyma by bacteria culture. The histological features of skin lesions were normal. The detection of T lymphocyte subtype wes shown as: CD3 (32%), CD4 (27%), CD8 (20%). The ratio of CD4/CD8 was 1.35. She was treated with systemic and topical antibiotics, immunoloregulation medicine, antianemia drugs, et al. Then the abnormity in immunoassay and the ecthyma were disappeared. The iron deficiency anemia was cured.
出处
《临床皮肤科杂志》
CAS
CSCD
北大核心
2003年第12期720-721,共2页
Journal of Clinical Dermatology
关键词
皮肤弹性过度
细胞免疫缺陷
cutis hyperelastica
cellular immunodeficiency
