Objective
Idiopathic granulomatous mastitis (IGM) is a rare benign chronic inflammatory breast disease. Although the etiology is unknown, some conditions such as autoimmune diseases, infectious causes, hormonal disorders and pregnancy are blamed. Cellular or humoral immune system disorders may be seen in patients. Cytokines are proteins involved in immune function, inflammation and wound healing. Interleukin (IL) −4; is released from T cells and mast cells and is the most important stimulant of immunoglobulin E production. IL-8; is released from macrophages and is responsible for chemotaxis. IL-10 acts as an inhibitor in the control of the immune response. IL-17 plays a proinflammatory role. TNF-α is the most important mediator of acute inflammatory response. The aim of this study was to evaluate the levels of IL-4, IL-8, IL-10, IL-17 and TNF-alpha in patients diagnosed with IGM.
Materials and Methods
47 patients with pathologic diagnosis of IGM and 30 healthy volunteers were included in the study. Patients were divided into two groups as “active” and “in remission. Serum IL-4, IL-8, IL-10, IL-17 and TNF-α levels were measured by ELISA.
Results
Of 47 patients diagnosed with idiopathic granulomatous mastitis, 21 had active lesions. There was no difference in IL-4 levels between the patient and control groups. IL-8, IL-10, IL-17 levels were significantly higher in the patient group compared to the control group. IL-8 levels were significantly higher in patients with active disease than those in remission; IL-10 levels were higher in patients in remission and the difference was statistically significant. Serum TNF-α levels were higher in the control group but not statistically significant.
Conclusion
The association of idiopathic granulomatous mastitis with rheumatologic symptoms and diseases suggests immune dysregulation and autoimmunity in the etiology. In this study, we investigated IL-4, IL-8, IL-10, IL-17 and TNF-α levels in order to shed light on etiopathogenesis. The results show that immune dysregulation has an effect on the development and control of the disease. Further studies are needed to determine the effect of these markers on prognosis. In addition, this study will shed light on the use of monoclonal antibodies against cytokines in the treatment of resistant patients.
