Özet:

Common variable immunodeficiency (CVID) is a primary immunodeficiency syndrome characterized by recurring bacterial infections and hypogammaglobulinemia that can occur at any age. Our first phenomenon;27 years old lady sick.Psöriasis present patient for 1 week with continued fever,diarrheal cough,sickness,sickness complaints.In his examination splenomegali was found.In the liver graph and in HRCT bilateral alveoler consolidation and pleural fusion was detected.Torasentez was detected and torace tube drainage was applied.Inmunoglobulin(IgG,IgM,IgA) levels were advance low in patients with CVID diagnosis and intravenous Ig(IV) treatment was applied. The second phenomenon is a 57-year-old male. For the first time in 2010 the pleural biopsy resulted in non-necrotizan granulomatosis disease resulted in 9 months of antibacterial treatment due to repeated hemopathy 2 times in our clinic due to malignity taken in the PET-CT in the left lungs lower lobby inflammation was identified in harmful attitude.Broncoscopic and laboratory examinations were not detected malignity,vascillitis and tuberculosis.In the 7th month of 2012 the patient reinserted due to pleural erection was in harmful with the pleural amphemy taken with torasenthes, the ultrasonic torasenthes were detected and the drug was detected.Immggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggggg The patient was diagnosed with CVID and IVIG was applied after toracoscopy and followed. CVID should be taken into account in repeated, complicated community-based pneumons accompanied by autoimmune diseases such as psoriasis, splenomegali and sarkoid-like granulomatosis diseases.

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