Ong Seeu Si, Sim Jean Xiang Ying, Chan Ching-Wan, Ho Peh Joo, Lim Zi Lin, Hartman Mikael, Li Jingmei
Genome Institute of Singapore (GIS), Agency for Science, Technology and Research (A∗STAR), Singapore, 138672, Singapore.
Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore and National University Health System, Singapore, 119228, Singapore.
Heliyon. 2024 Sep 24;10(19):e38345. doi: 10.1016/j.heliyon.2024.e38345. eCollection 2024 Oct 15.
Idiopathic granulomatous mastitis (IGM) is a rare, chronic inflammatory breast condition primarily affecting women of reproductive age. Its diagnosis is challenging due to similarities with other breast disorders, necessitating exclusion of other granulomatous diseases. The management of IGM remains inconsistent and unclear, with high recurrence rates and varying practices.
This qualitative study involved semi-structured interviews with nine clinicians from Singapore, Malaysia, and Egypt to examine current diagnostic and therapeutic approaches for IGM. Transcripts were analysed using NVivo software for coding and summarisation.
Clinicians predominantly used imaging and histopathology for diagnosis. Treatment commonly involved corticosteroids, though dosages and tapering regimens varied widely. Methotrexate was used sparingly for refractory cases due to associated risks. Surgical interventions were infrequent, reflecting a preference for medical management. There was a consensus on the need for randomised controlled trials (RCTs) to establish standardised treatment protocols.
This study reveals the complex nature of IGM diagnosis and treatment from clinicians in Singapore, Malaysia and Egypt. This underscores the need for more specific and definitive diagnostic tests, rather than relying on exclusionary methods, and standardised treatment guidelines. Multi-centre RCTs are essential for developing evidence-based protocols to improve patient outcomes and address regional differences effectively.
特发性肉芽肿性乳腺炎(IGM)是一种罕见的慢性炎症性乳腺疾病,主要影响育龄女性。由于与其他乳腺疾病相似,其诊断具有挑战性,需要排除其他肉芽肿性疾病。IGM的治疗仍然不一致且不明确,复发率高且治疗方法各异。
这项定性研究对来自新加坡、马来西亚和埃及的9名临床医生进行了半结构化访谈,以研究IGM目前的诊断和治疗方法。使用NVivo软件对访谈记录进行编码和总结分析。
临床医生主要使用影像学和组织病理学进行诊断。治疗通常涉及使用皮质类固醇,尽管剂量和逐渐减量方案差异很大。由于相关风险,甲氨蝶呤仅用于难治性病例。手术干预很少,这反映出对药物治疗的偏好。对于需要进行随机对照试验(RCT)以建立标准化治疗方案已达成共识。
本研究揭示了新加坡、马来西亚和埃及临床医生对IGM诊断和治疗的复杂性。这强调了需要更具体、明确的诊断测试,而不是依赖排除性方法,以及标准化治疗指南。多中心RCT对于制定基于证据的方案以改善患者预后并有效解决地区差异至关重要。