FRI0500 Idiopathic Granulomatous Mastitis: A Single Center Experience. (15th July 2016)
- Record Type:
- Journal Article
- Title:
- FRI0500 Idiopathic Granulomatous Mastitis: A Single Center Experience. (15th July 2016)
- Main Title:
- FRI0500 Idiopathic Granulomatous Mastitis: A Single Center Experience
- Authors:
- Cinar, M.
Yilmaz, S.
Cakar, M.
Pay, S. - Abstract:
- Abstract : Background: Idiopathic granulomatous mastitis (IGM) is a rare benign inflammatory disease of the breast. Difficulties can be experienced in the treatment of IGM due to the lack of a common consensus in the literature. Treatment options include corticosteroids, surgical treatment, immunosuppressive drugs and conservative treatment with antibiotics. Objectives: To present our experience about patients with IGM on immunosuppressive therapy. Methods: The data of patients with a diagnosis of IGM under immunosuppressive therapy followed in the rheumatology outpatient clinic of a tertiary center enrolled between September 2010 and August 2015 were evaluated retrospectively. 16 histopathologically diagnosed patients receiving immunosuppressive therapy were evaluated for their treatments and treatment responses. Results: The mean age of the patients, the average duration of immunosuppressive therapy and the average follow-up period were 35.9±6.5 years, 19.6±14.1 months and 28.3±17.8 months, respectively. Initially, 15 patients received (93.8%) steroids and methotrexate, and 1 patient (6.2%) was treated only with steroids. All patients responded well to initial therapy. Eight (53.3%) patients achieved remission with steroid + methotrexate. 2 of the other 7 patients relapsed after discontinuation of steroids and 1 after discontinuation of steroid + methotrexate. A positive response was obtained after the restart of treatment with steroids and methotrexate in these patients.Abstract : Background: Idiopathic granulomatous mastitis (IGM) is a rare benign inflammatory disease of the breast. Difficulties can be experienced in the treatment of IGM due to the lack of a common consensus in the literature. Treatment options include corticosteroids, surgical treatment, immunosuppressive drugs and conservative treatment with antibiotics. Objectives: To present our experience about patients with IGM on immunosuppressive therapy. Methods: The data of patients with a diagnosis of IGM under immunosuppressive therapy followed in the rheumatology outpatient clinic of a tertiary center enrolled between September 2010 and August 2015 were evaluated retrospectively. 16 histopathologically diagnosed patients receiving immunosuppressive therapy were evaluated for their treatments and treatment responses. Results: The mean age of the patients, the average duration of immunosuppressive therapy and the average follow-up period were 35.9±6.5 years, 19.6±14.1 months and 28.3±17.8 months, respectively. Initially, 15 patients received (93.8%) steroids and methotrexate, and 1 patient (6.2%) was treated only with steroids. All patients responded well to initial therapy. Eight (53.3%) patients achieved remission with steroid + methotrexate. 2 of the other 7 patients relapsed after discontinuation of steroids and 1 after discontinuation of steroid + methotrexate. A positive response was obtained after the restart of treatment with steroids and methotrexate in these patients. Of these 7 patients, no recurrence was observed in 3 (42.9%) patients with only methotrexate and in 4 (57.1%) patients in the maintenance treatment with steroids and methotrexate. Lowered dose of steroid was associated with recurrence during follow-up of the patient taking only steroids as the initial treatment. 5 patients (33.3%) taking methotrexate had drug side effects, not necessitate stopping the treatment. Conclusions: Systemic immunosuppressive therapy is safe and effective in IGM. Azathioprine and methotrexate have been the most frequently used immunosuppressive drugs in the literature. Our experience with methotrexate-based regimen allows the rapid reduction of the steroid dose and leads to remission. References: Konan A, Kalyoncu U, Dogan I, Kiliç YA, Karakoç D, Akdogan A, Kiraz S, Kaynaro Lu V, Onat D. Combined long-term steroid and immunosuppressive treatment regimen in granulomatous mastitis. Breast Care (Basel). 2012 Aug;7(4):297–301. Sheybani F, Sarvghad M, Naderi HR, Gharib M. Treatment for and clinical characteristics of granulomatous mastitis.Obstet Gynecol. 2015 Apr;125(4):801–7. Disclosure of Interest: None declared … (more)
- Is Part Of:
- Annals of the rheumatic diseases. Volume 75(2016)Supplement 2
- Journal:
- Annals of the rheumatic diseases
- Issue:
- Volume 75(2016)Supplement 2
- Issue Display:
- Volume 75, Issue 2 (2016)
- Year:
- 2016
- Volume:
- 75
- Issue:
- 2
- Issue Sort Value:
- 2016-0075-0002-0000
- Page Start:
- 619
- Page End:
- 619
- Publication Date:
- 2016-07-15
- Subjects:
- Rheumatism -- Periodicals
616.723005 - Journal URLs:
- http://ard.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=149&action=archive ↗
http://www.bmj.com/archive ↗
http://gateway.ovid.com/server3/ovidweb.cgi?T=JS&MODE=ovid&D=ovft&PAGE=titles&SEARCH=annals+of+the+rheumatic+diseases.tj&NEWS=N ↗ - DOI:
- 10.1136/annrheumdis-2016-eular.5289 ↗
- Languages:
- English
- ISSNs:
- 0003-4967
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 18012.xml