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Abstract Idiopathic granulomatous mastitis is a rare benign breast disease. The prevalence of Granulomatous Mastitis is generally reported at less than 1% worldwide among women presenting with breast problems however, reports vary greatly by country and ethnic group and a study of granulomatous mastitis (GM) in the United States demonstrated a prevalence of less than 1% among women who underwent biopsy for breast diseases. In the UK, it was found in 0.98% of patients presenting at the breast unit. IGLM is a rare chronic non-specific inflammatory disease of the breast that mimics cancer both clinically and mammographically. Originally described by Kessler and Wolloch in 1972. The etiology of idiopathic granulomatous mastitis is still obscure.The cause may be the autoimmune process, infection, a chemical reaction associated with oral contraceptive pills, or even lactation. Various factors, including hormonal imbalance, autoimmunity, unknown microbiological agents, smoking and α 1-antitrypsin deficiency have been suggested to play a role in disease aetiology.It has been considered as rare, chronic, nonspecific granulomatous process, affecting the breast in relatively young patients, especially parous women as a tender, unilateral, firm, discrete extra-areolar breast lump in a lobular distribution, often associated with inflammation of the overlying skin. Patients are almost always afebrile and might present with multiple areas of simultaneous peripheral infection with abscesses and or inflammation of the skin overlying the region and ulceration or sinus formation. The granulomas in granulomatous mastitis have been described as noncaseating granulomas,consisting of epithelioid histiocytes and multinucleated giant cells that are surrounded by lymphocytes and plasma cells. Frequently, the granulomas became confluent with central suppuration and liquefaction necrosis. Granulomatous mastitis can mimic breast carcinoma clinically and mammographically, thus making an accurate preoperative diagnosis difficult. However, the sonographic appearance of multiple clustered, often contiguous tubular hypoechoic lesions that are sometimes associated with a large hypoechoic mass should suggest the possibility of granulomatous mastitis.Clinical and radiological findings are insufficient for diagnosis of IGLM as they are not disease specific and so the diagnosis of IGM requires a multidisciplinary approach, incorporating clinical, radiological, microbiological and pathological findings. Lesions identified clinically and radiologically could easily be misdiagnosed as carcinoma. Therefore, histopathological evaluation plays a very important role in differentiating these lesions from other granulomatous conditions, inflammatory changes, and carcinoma. A definitive diagnosis of IGLM can be made by FNAC, core biopsy or incisional and excisional biopsy. Although IGM as a disease has been known for nearly four decades, there is no consensus regarding the first-line treatment modality. Several treatment options have been described (antibiotics with repeated drainage, wide surgical excision or mastectomy, oral steroids, immunosuppression with methotrexate, and close follow-up), and successful results have been reported for each of these options. Currently, the most frequently employed treatment options are surgical treatment and systemic steroid treatment. Wide surgical excision is more beneficial than limited excision in patients with localized disease as limited excision alone is associated with a strong tendency for persistence or recurrence.A course of oral steroids, nonsteroidal anti‐ inflammatory drugs, or colchicine can be used in order to shrink the breast mass, allowing more conservative surgery. On the other hand, the initiation of steroids is often limited by concerns related to the presence of an infectious etiology.The role of incision&drainage is controversial because it may lead to increased scarring and nonhealing of incision tracks, which subsequently leads to formation of sinus tracks. |