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Evaluation of Pulmonary Complications in Patients With Primary Immunodeficiency Disorders Pubmed



Reisi M1 ; Azizi G2, 3 ; Kiaee F3 ; Masiha F4 ; Shirzadi R4 ; Momen T5 ; Rafiemanesh H6 ; Tavakolinia N3 ; Modaresi M4 ; Aghamohammadi A3
Authors
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Authors Affiliations
  1. 1. Pediatric Pulmonology Department, Child Growth and Development Research Center, Research Institute of Primordial Prevention of non-communable Disease, Isfahan University of medical sciences, Isfahan, Iran
  2. 2. Department of Laboratory Medicine, Imam Hassan Mojtaba Hospital, Alborz University of Medical Sciences, Karaj, Iran
  3. 3. Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Pediatric Pulmonary Department, Pediatrics Center of Excellence, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Pediatric Immunology, Allergy and Asthma Department, Child Growth and Development Research Center, Research Institute of Primordial Prevention of Non-Communable Disease, Isfahan University of Medical Sciences, Isfahan, Iran
  6. 6. Department of Epidemiology, School of Public Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Source: European Annals of Allergy and Clinical Immunology Published:2017


Abstract

Background. Primary immunodeficiencies (PIDs) are inherited disorders in which one or several components of immune system are defected. Moreover, affected patients are at high risk for developing recurrent infections, particularly pulmonary infections. The spectrum of pulmonary manifestations in PIDs is broad, and includes acute and chronic infection, structural abnormalities (eg, bronchiectasis), malignancy and dysregulated inflammation resulting in tissue damage. In this study, our aims are to evaluate pulmonary complications in PID patients. Patients and Methods. We studied 204 cases with confirmed PID. To evaluate pulmonary complications in these patients, we used pulmonary function test (PFT), high resolution computed tomography (HRCT) scan and bronchoalveolar lavage (BAL). Results. Our results showed that pneumonia was the most frequent clinical manifestations in all PID patients. There were significantly greater numbers of episodes of pneumonia in HIgM, XLA and CVID patients with delayed diagnoses < 6 years. Moreover, of 57.4% CVID patients, 55% XLA patients and 33.3% HIgM patients had abnormal PFT results, and bronchiectasis was showed in 9 (42.9%) of XLA, 6 (11.8%) of HIES, 3 (21.4%) of HIgM and 38 (62.3%) of CVID patients. Conclusion. Pulmonary complications should be considered in cases with PIDs especially in CVID cases. © 2017, EDRA LSWR. All rights reserved.
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6. The Use of Immunoglobulin Therapy in Primary Immunodeficiency Diseases, Endocrine# Metabolic and Immune Disorders - Drug Targets (2016)
7. Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment, Journal of Investigational Allergology and Clinical Immunology (2015)
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