Yaghan Rami J, Ayoub Nehad M, Hamouri Shadi, Al-Mohtaseb Alia, Gharaibeh Maha, Yaghan Lamees, Al-Dari Mahmoud, Al-Kaff Hiba, Al-Zoubi Nabil A
Department of Surgery, College of Medicine and Medical Sciences, Arabian Gulf University, Manama, Bahrain.
Department of Surgery and Urology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
Int J Breast Cancer. 2020 Jan 27;2020:5243958. doi: 10.1155/2020/5243958. eCollection 2020.
Iidiopathic granulomatous mastitis (IGM) is stereotypically described as a mysterious entity that mimics breast carcinoma imposing management challenges. In 2002, we established a multidisciplinary team to treat patients with IGM. This study aimed to evaluate the role of this team in improving patient outcomes. Also, a review of literature is provided to highlight recent disease trends. . Pertinent data for 44 patients treated for IGM from 2002 to 2018 were analyzed and compared to data prior to 2002.
Mean age at diagnosis was 37.9 years ± 6.4. The diagnosis of IGM was confirmed by True-cut biopsy (TCB), Frozen section (FS), and surgical biopsy in 70.5%, 25%, and 4.5% of patients, respectively. FS was used to assess the resection margins in three patients. Suspicion for malignancy was raised in one out of 39 ultrasound reports, and one out of 20 mammography reports. Wide local excision was the main treatment modality (95.5%). 19 patients (43.2%) received corticosteroids. Prior to 2002, IGM was only recognized after surgical resection with a 71% initial false impression of carcinoma. After 2002, the initial false clinical impression of carcinoma dropped to 29.5%. Recurrence rate was 31.82%. Younger age at diagnosis was significantly associated with recurrence ( = 5.598; = 0.018). Chi-square analysis showed no significant association between BMI and recurrence ( = 0.776; = 0.678).
The establishment of a multidisciplinary team for IGM was associated with a reduced erroneous impression of breast cancer, and a reduced false positive radiological diagnosis of breast carcinoma. FS was a useful confirmatory procedure. Our series included the first case of a diffuse papular rash as a systemic manifestation of IGM. Recent literature indicates that IGM is changing its face. IGM is being reported in all age groups, and even in males. The clinical manifestations have markedly expanded. Diagnosis by TCB has replaced blind surgical excision. More data regarding predictors of recurrence is accumulating.
特发性肉芽肿性乳腺炎(IGM)通常被描述为一种神秘的疾病,它类似于乳腺癌,给治疗带来了挑战。2002年,我们成立了一个多学科团队来治疗IGM患者。本研究旨在评估该团队在改善患者治疗效果方面的作用。此外,还对文献进行了综述,以突出近期的疾病趋势。分析了2002年至2018年期间接受IGM治疗的44例患者的相关数据,并与2002年之前的数据进行了比较。
诊断时的平均年龄为37.9岁±6.4岁。分别有70.5%、25%和4.5%的患者通过粗针活检(TCB)、冰冻切片(FS)和手术活检确诊为IGM。3例患者使用FS评估切除边缘。39份超声报告中有1份、20份乳腺X线摄影报告中有1份怀疑为恶性肿瘤。广泛局部切除是主要的治疗方式(95.5%)。19例患者(43.2%)接受了皮质类固醇治疗。2002年之前,IGM只有在手术切除后才被认识到,最初误诊为癌的比例为71%。2002年之后,最初误诊为癌的临床假象降至29.5%。复发率为31.82%。诊断时年龄较小与复发显著相关(χ²=5.598;P=0.018)。卡方分析显示BMI与复发之间无显著相关性(χ²=0.776;P=0.678)。
IGM多学科团队的建立与乳腺癌错误印象的减少以及乳腺癌放射学假阳性诊断的减少有关。FS是一种有用的确诊方法。我们的系列病例包括第一例弥漫性丘疹性皮疹作为IGM全身表现的病例。近期文献表明IGM正在改变其面貌。各年龄组甚至男性中都有IGM的报道。临床表现明显扩大。TCB诊断已取代盲目手术切除。关于复发预测因素的更多数据正在积累。