Key result
Appropriate therapy resolves rare pericardial effusion in a teen with common variable immunodeficiency.
Case Report (n=1)
Highlights that pericardial effusion can occur as a rare cardiac complication in patients with Common Variable Immunodeficiency even in the absence of autoimmune disease.
Clinicians may consider pericardial effusion in CVID without autoimmunity; single case leaves association and prevalence hypothesis-generating.
A Patient With Common Variable Immunodeficiency and Pericardial EffusionIntroduction: 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.
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Payandeh et al. (2019) conducted a case report in Common Variable Immunodeficiency (CVID) and Pericardial Effusion (n=1). Intravenous immunoglobulin and prophylactic antibiotics was evaluated on Clinical, radiographic and physiological improvements. A 17-year-old girl with common variable immunodeficiency developed a rare pericardial effusion in the absence of autoimmune disease, which resolved with appropriate therapy.
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