دوره 7، شماره 3 - ( 4-1398 )                   جلد 7 شماره 3 صفحات 180-177 | برگشت به فهرست نسخه ها


XML English Abstract 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-fa.html
A Patient With Common Variable Immunodeficiency and Pericardial Effusion: A Case Report and Review of Literature. Journal of Pediatrics Review. 1398; 7 (3) :177-180

URL: http://jpr.mazums.ac.ir/article-1-182-fa.html


چکیده:   (5226 مشاهده)
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.
متن کامل [PDF 375 kb]   (2070 دریافت)    
نوع مطالعه: Case & Review |
دریافت: 1397/2/23 | پذیرش: 1397/5/27 | انتشار: 1398/4/10

ارسال نظر درباره این مقاله : نام کاربری یا پست الکترونیک شما:
CAPTCHA

بازنشر اطلاعات
Creative Commons License این مقاله تحت شرایط Creative Commons Attribution-NonCommercial 4.0 International License قابل بازنشر است.

کلیه حقوق این وب سایت متعلق به Journal of Pediatrics Review می باشد.

طراحی و برنامه نویسی : یکتاوب افزار شرق

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

Designed & Developed by : Yektaweb