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巴基斯坦一家三级医疗中心原发性免疫缺陷患者的临床和实验室特征

Clinical and Laboratory Characteristics of Primary Immunodeficiency Patients from a Tertiary Care Center in Pakistan.

作者信息

Tipu Hamid Nawaz, Ahmed Dawood

机构信息

Department of Immunology, Armed Forces Institute of Pathology, Rawalpindi, Pakistan.

出版信息

J Pak Med Assoc. 2020 Dec;70(12(B)):2403-2407. doi: 10.47391/JPMA.512.

Abstract

OBJECTIVE

The aim of this study was to describe and identify clinical presentation of primary immunodeficiency disorders (PIDs). Characteristic quantitative and qualitative immunological abnormalities have been described which help in establishing a definitive PID diagnosis.

METHODS

This was a cross sectional study conducted in the Immunology department of the Armed Forces Institute of Pathology, Rawalpindi, Pakistan, from Jan 2016 to Dec 2018. Sixty patients of different PIDs including humoral defects, combined immunodeficiency, phagocytic defects and other miscellaneous disorders, were diagnosed over a period of 3 years in our institute. Their clinical presentation and laboratory data are presented in this study.

RESULTS

In 3 years, 40 (66%) males and 20 (33%) females were diagnosed, with 13 (21.6%) patients of humoral deficiency, 22 (36.6%) of severe combined immunodeficiency, 18 (30%) of phagocytic defects and 7 (11.6%) of other miscellaneous disorders. Maximum patients belonged to Punjab province, i.e., 23 (38.3%). Their mean age for initiation of symptoms was 7±12.6 months, while diagnosis was made at mean age of 26±39.28 months, in all groups combined. Respiratory infections were commonest presentation, in 46 (76.6%) patients. Also 46 (76.6%) patients had consanguineous parents. Presence of family history of PID in 27 (45%) patients was not associated with an earlier diagnosis (p 0.955). Each group of patients carried characteristic laboratory findings.

CONCLUSIONS

PIDs should be suspected in offsprings with warning signs coming from consanguineous parents. There is a need to introduce genetic diagnosis of PIDs in order to timely diagnose less characteristic PID presentations.

摘要

目的

本研究旨在描述和识别原发性免疫缺陷病(PID)的临床表现。已描述了有助于明确PID诊断的特征性定量和定性免疫异常。

方法

这是一项横断面研究,于2016年1月至2018年12月在巴基斯坦拉瓦尔品第武装部队病理研究所免疫科进行。在我们研究所的3年时间里,诊断出60例不同类型的PID患者,包括体液免疫缺陷、联合免疫缺陷、吞噬细胞缺陷和其他杂类疾病。本研究展示了他们的临床表现和实验室数据。

结果

3年间,共诊断出40名男性(66%)和20名女性(33%),其中体液免疫缺陷患者13名(21.6%),严重联合免疫缺陷患者22名(36.6%),吞噬细胞缺陷患者18名(30%),其他杂类疾病患者7名(11.6%)。患者最多的是旁遮普省,即23名(38.3%)。所有组综合起来,症状开始出现的平均年龄为7±12.6个月,而诊断时的平均年龄为26±39.28个月。呼吸道感染是最常见的表现,有46名(76.6%)患者出现。此外,46名(76.6%)患者的父母为近亲。27名(45%)患者有PID家族史,但这与更早诊断无关(p = 0.955)。每组患者都有特征性的实验室检查结果。

结论

对于有来自近亲父母的警示信号的后代,应怀疑患有PID。有必要引入PID的基因诊断,以便及时诊断出特征性不明显的PID表现。

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