Literature DB >> 33969305

Imaging Features of Primary Immunodeficiency Disorders.

Jose A Rodriguez1, Tami J Bang1, Carlos S Restrepo1, Daniel B Green1, Lorna P Browne1, Daniel Vargas1.   

Abstract

Primary immunodeficiency disorders (PIDs), which are humoral, combined, and innate defects of the immune system, are relatively uncommon and may go undiagnosed in patients experiencing recurrent infections, resulting in increased morbidity and mortality. PIDs are clinically characterized by a broad spectrum of disorders, including repeated infections, autoimmune disorders, lymphoproliferative diseases, congenital anomalies, and increased risk of malignancy. Cardiothoracic imaging plays a crucial role in the diagnosis of PIDs owing to the high rates of repeated respiratory infections leading to bronchiectasis and other forms of chronic lung disease. Although PIDs as a group may seem similar in terms of radiologic features and clinical manifestations, there are specific entities that are pertinent to each PID on an individual level. For example, patients with common variable immunodeficiency may develop a unique granulomatous lymphocytic interstitial lung disease, and Good syndrome is associated with thymoma. Familiarity with the imaging characteristics of these disorders may expedite diagnosis and prognostication, and better direct therapy. Reviewing the thoracic manifestations of all PIDs is beyond the scope of this article; thus, the focus herein is on discussing the thoracic manifestations of the most common PIDs and their imaging features. © RSNA, 2021An earlier incorrect version appeared online. This article was corrected on March 25, 2021. 2021 by the Radiological Society of North America, Inc.

Entities:  

Year:  2021        PMID: 33969305      PMCID: PMC8098094          DOI: 10.1148/ryct.2021200418

Source DB:  PubMed          Journal:  Radiol Cardiothorac Imaging        ISSN: 2638-6135


  46 in total

Review 1.  The immune deficiency of chromosome 22q11.2 deletion syndrome.

Authors:  Megan Morsheimer; Terri F Brown Whitehorn; Jennifer Heimall; Kathleen E Sullivan
Journal:  Am J Med Genet A       Date:  2017-06-19       Impact factor: 2.802

2.  [Clinical phenotypes associated with selective IgA deficiency: a review of 330 cases and a proposed follow-up protocol].

Authors:  O Domínguez; M T Giner; L Alsina; M A Martín; J Lozano; A M Plaza
Journal:  An Pediatr (Barc)       Date:  2012-01-11       Impact factor: 1.500

3.  Respiratory Complications in Patients with Hyper IgM Syndrome.

Authors:  Bobak Moazzami; Reza Yazdani; Gholamreza Azizi; Fatemeh Kiaei; Mitra Tafakori; Mohammadreza Modaresi; Rohola Shirzadi; Seyed Alireza Mahdaviani; Mahsa Sohani; Hassan Abolhassani; Asghar Aghamohammadi
Journal:  J Clin Immunol       Date:  2019-06-11       Impact factor: 8.317

4.  Evaluation of respiratory complications in patients with X-linked and autosomal recessive agammaglobulinemia.

Authors:  Saba Fekrvand; Reza Yazdani; Peter Olbrich; Gholamreza Azizi; Rohola Shirzadi; Mohammadreza Modaresi; Mahsa Sohani; Samaneh Delavari; Arash Kalantari; Mansoureh Shariat; Alireza Shafiei; Na Lu; Gholamreza Hassanpour; Maziar Rahimi Hajiabadi; Parisa Ashournia; Anahita Razaghian; Marzieh Asgharyan; Zahra Shahraki-Ghadimi; Roja Rouhani; Fatemeh Hoda Fallah; Nima Rezaei; Hassan Abolhassani; Asghar Aghamohammadi
Journal:  Pediatr Allergy Immunol       Date:  2020-03-06       Impact factor: 6.377

Review 5.  Spectrum of imaging findings of chronic granulomatous disease: a single center experience.

Authors:  Minah Lee; Mu Sook Lee; Jeong Sub Lee; Su Yeon Ko; Sun Young Jeong
Journal:  Diagn Interv Radiol       Date:  2017 Nov-Dec       Impact factor: 2.630

6.  Autosomal Dominant Hyper-IgE Syndrome in the USIDNET Registry.

Authors:  Yael Gernez; Alexandra F Freeman; Steven M Holland; Elizabeth Garabedian; Niraj C Patel; Jennifer M Puck; Kathleen E Sullivan; Javeed Akhter; Elizabeth Secord; Karin Chen; Rebecca Buckley; Elie Haddad; Hans D Ochs; Ramsay Fuleihan; John Routes; Mica Muskat; Patricia Lugar; Julien Mancini; Charlotte Cunningham-Rundles
Journal:  J Allergy Clin Immunol Pract       Date:  2017-09-19

7.  A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing.

Authors:  Cheng-Yu Liao; Hui-Wen Yu; Chao-Neng Cheng; Jiann-Shiuh Chen; Ching-Wei Lin; Peng-Chieh Chen; Chi-Chang Shieh
Journal:  J Microbiol Immunol Infect       Date:  2018-03-02       Impact factor: 4.399

8.  Combined immunodeficiencies: twenty years experience from a single center in Turkey.

Authors:  H Haluk Akar; Turkan Patiroglu; Michael Hershfield; Mirjam van der Burg
Journal:  Cent Eur J Immunol       Date:  2016-01-20       Impact factor: 2.085

9.  Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia: Report from Shanghai, China (2000-2015).

Authors:  Xia-Fang Chen; Wei-Fan Wang; Yi-Dan Zhang; Wei Zhao; Jing Wu; Tong-Xin Chen
Journal:  Medicine (Baltimore)       Date:  2016-08       Impact factor: 1.889

10.  Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification.

Authors:  Aziz Bousfiha; Leila Jeddane; Capucine Picard; Waleed Al-Herz; Fatima Ailal; Talal Chatila; Charlotte Cunningham-Rundles; Amos Etzioni; Jose Luis Franco; Steven M Holland; Christoph Klein; Tomohiro Morio; Hans D Ochs; Eric Oksenhendler; Jennifer Puck; Troy R Torgerson; Jean-Laurent Casanova; Kathleen E Sullivan; Stuart G Tangye
Journal:  J Clin Immunol       Date:  2020-02-11       Impact factor: 8.317

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.