Volume 7, Issue 3 (7-2019)                   J. Pediatr. Rev 2019, 7(3): 177-180 | Back to browse issues page


XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Payandeh P, Khoshkhui M, Jabbari Azad F, Farid Hosseini R. A Patient With Common Variable Immunodeficiency and Pericardial Effusion: A Case Report and Review of Literature. J. Pediatr. Rev 2019; 7 (3) :177-180
URL: http://jpr.mazums.ac.ir/article-1-182-en.html
1- Department of Immunology and Allergy, School of Medicine, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.
2- Allergy Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. , arc@mums.ac.ir
3- Allergy Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Abstract:   (5597 Views)
Introduction: Common Variable Immunodeficiency (CVID) is one of the primary immunodeficiencies that its patients can develop its symptoms since infancy till senility; however, it usually manifests between the age of 15 and 40 years. It is characterized by low antibody levels and recurrent infections.  Individuals with CVID are more prone to autoimmune diseases and malignancy.
Case presentation: We presented a 17-year-old girl with a documented CVID, who was treated with intravenous immunoglobulin and prophylactic antibiotics.  She suffered from CVID from the age of 13 to the study time. She was hospitalized due to illness, fever, and severe dyspnea. Her chest X-ray revealed cardiomegaly; thus, high-resolution thorax CT scan and echocardiography were performed which revealed pericardial effusion. No underlying autoimmune diseases were detected in our assessments. Significant clinical, radiographic and physiological improvements were achieved after conducting an appropriate therapy. The patient was followed for two years and showed no clinical and laboratory findings in respect to autoimmune diseases. In our case, the pericardial effusion was present without any evidence of autoimmunity.
Conclusions: Cardiac manifestation and complications are rare in CVID patients in the absence of an autoimmune disease; however, they should be considered.
Full-Text [PDF 375 kb]   (2193 Downloads) |   |   Full-Text (HTML)  (1633 Views)  
Type of Study: Case & Review | Subject: Immunology
Received: 2018/05/13 | Accepted: 2018/08/18 | Published: 2019/07/1

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 CC BY-NC 4.0 | Journal of Pediatrics Review

Designed & Developed by : Yektaweb