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原发性免疫缺陷病

Primary immunodeficiencies.

作者信息

Cooper Megan A, Pommering Thomas L, Korányi Katalin

机构信息

The Ohio State University College of Medicine and Public Health, Columbus, Ohio, USA.

出版信息

Am Fam Physician. 2003 Nov 15;68(10):2001-8.

Abstract

Primary immunodeficiencies include a variety of disorders that render patients more susceptible to infections. If left untreated, these infections may be fatal. The disorders constitute a spectrum of more than 80 innate defects in the body's immune system. Primary immunodeficiencies generally are considered to be relatively uncommon. There may be as many as 500,000 cases in the United States, of which about 50,000 cases are diagnosed each year. Common primary immunodeficiencies include disorders of humoral immunity (affecting B-cell differentiation or antibody production), T-cell defects and combined B- and T-cell defects, phagocytic disorders, and complement deficiencies. Major indications of these disorders include multiple infections despite aggressive treatment, infections with unusual or opportunistic organisms, failure to thrive or poor growth, and a positive family history. Early recognition and diagnosis can alter the course of primary immunodeficiencies significantly and have a positive effect on patient outcome.

摘要

原发性免疫缺陷包括多种使患者更易感染的病症。若不治疗,这些感染可能会致命。这些病症构成了人体免疫系统中80多种先天性缺陷的范围。原发性免疫缺陷通常被认为相对不常见。美国可能有多达50万例病例,其中每年约有5万例被诊断出来。常见的原发性免疫缺陷包括体液免疫障碍(影响B细胞分化或抗体产生)、T细胞缺陷以及B细胞和T细胞联合缺陷、吞噬细胞疾病和补体缺陷。这些病症的主要指征包括尽管积极治疗仍反复感染、感染不常见或机会性生物体、生长发育不良或生长缓慢以及家族史阳性。早期识别和诊断可显著改变原发性免疫缺陷的病程,并对患者的预后产生积极影响。

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