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一家三级医疗医院原发性免疫缺陷的谱系

Spectrum of primary immune deficiency at a tertiary care hospital.

作者信息

Verma Sumit, Sharma Pradeep Kumar, Sivanandan Sindhu, Rana Nidhi, Saini Savita, Lodha Rakesh, Kabra S K

机构信息

Department of Pediatrics, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.

出版信息

Indian J Pediatr. 2008 Feb;75(2):143-8. doi: 10.1007/s12098-008-0022-9.

Abstract

OBJECTIVE

To report various primary immune deficiencies diagnosed in children at a tertiary care hospital, their clinical manifestations and laboratory profile.

METHODS

Case records of children diagnosed to have primary immunodeficiency disorders over a period of 24 months at a tertiary care hospital in northern India were evaluated.

RESULTS

Twenty-seven children (M: F=3.5: 1) with mean age of 5.4 +/- 4.6 yrs (2 mo-16 yr) were diagnosed to have primary immunodeficiency. Thirteen children had chronic granulomatous disease (CGD), 4 had severe combined immunodeficiency (SCID), 4 had hypogammaglobulinemia, 2 had Ataxia telangiectasia, and one each had DiGeorge syndrome, Wiskott Aldrich syndrome, hyper IgM syndrome and leukocyte adhesion defect. Common mode of presentation were recurrent/ persistent pneumonia in 19, recurrent/ persistent diarrhea in 10, deep seated abscesses in 8, allergy in 3, disseminated tuberculosis infection in 2, extensive fungal infections in 2 and 1 each of disseminated cytomegalovirus (CMV) infection, disseminated BCG disease, otitis media and meningitis. Family history of sibling deaths was elicited in 2 families. Infectious agents were isolated in 16 cases.

CONCLUSION

From a single center 27 patients with primary immune deficiency could be identified by chart review, suggesting need for high index of suspicion for diagnosis of primary immune deficiency in India. Though the exact prevalence is not known there is need to make a registry to document the magnitude of problem of these disorders.

摘要

目的

报告在一家三级医疗医院诊断出的儿童各种原发性免疫缺陷病、其临床表现及实验室检查结果。

方法

对印度北部一家三级医疗医院在24个月期间诊断为原发性免疫缺陷病的儿童病历进行评估。

结果

27名儿童(男:女 = 3.5:1)被诊断为原发性免疫缺陷病,平均年龄为5.4±4.6岁(2个月至16岁)。13名儿童患有慢性肉芽肿病(CGD),4名患有严重联合免疫缺陷病(SCID),4名患有低丙种球蛋白血症,2名患有共济失调毛细血管扩张症,各有1名患有迪格奥尔格综合征、维斯科特-奥尔德里奇综合征、高IgM综合征和白细胞黏附缺陷。常见的表现形式为:19例反复/持续肺炎,10例反复/持续腹泻,8例深部脓肿,3例过敏,2例播散性结核感染,2例广泛真菌感染,各1例播散性巨细胞病毒(CMV)感染、播散性卡介苗病、中耳炎和脑膜炎。2个家庭有同胞死亡的家族史。16例分离出感染病原体。

结论

通过病历审查,从一个单一中心可识别出27例原发性免疫缺陷患者,这表明在印度诊断原发性免疫缺陷需要高度怀疑。尽管确切患病率尚不清楚,但需要建立登记制度以记录这些疾病问题的严重程度。

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