Clinicopathological Evaluation of Idiopathic Granulomatous Mastitis: A Retrospective Analysis of Sixty Women at Shohada-e-Tajrish Hospital from 2010 to 2019

IF 0.4 Q4 ONCOLOGY
Azadeh Rakhshan, Atieh Akbari, Mahsa Ahadi, Hanieh Zham, Afshin Moradi, Kimia Karimi Toudeshki, Soroor Bashiri
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Abstract

Background: Idiopathic granulomatous mastitis (IGM) is an uncommon inflammatory disorder, which tends to occur in childbearing women. Although IGM has a benign nature, it can mimic a vast spectrum of diseases and may lead to an erroneous diagnosis of carcinoma. Also, the patients usually experience a prolonged course of the disease, which is distressing. But, the clinicopathological of IGM is nonspecific and not clear enough. Objectives: This study aims at evaluating the clinicopathological aspects of IGM. Methods: This cross-sectional retrospective study was performed in Shohada-e-Tajrish Hospital, Tehran, Iran on patients between 20 to 50 years old, preliminary diagnosed with IGM from 2010 to 2019. Then, the demographic, clinical, ultrasound, and histopathologic features of patients enrolled were evaluated. Results: A total number of 60 women aged 20 to 50 years old and initially diagnosed with IGM were enrolled in this study. Their mean age was 34.5 ± 6.73. Among all participants, 38.3% of patients had a family history of breast cancer. The most common location of the lesion was the upper outer quadrant (UOQ) with the predominance of the left side (36.6%). They were more likely to present with pain, erythema, swelling, and warmth (51.6%) of the breast followed by palpable mass (38.3%). With ultrasound assessment, the results were matched with a tubular hypoechoic mass in 43.3% of the patients, while the remainder showed a tumor-like lesion (21.6%) and abscess formation (15%). Histologically, non-caseating granulomas associated with mixed inflammatory cells (70%) and cystic space formations surrounded by neutrophil aggregations (15%) composed the dominant features. Conclusions: Despite the rarity of the disease, IGM is a diagnostic challenge as it can masquerade various breast conditions. A definite diagnosis needs collaboration of clinical, radiological, and histopathological findings.
特发性肉芽肿性乳腺炎的临床病理评价:2010 - 2019年Shohada-e-Tajrish医院60例妇女回顾性分析
背景:特发性肉芽肿性乳腺炎(IGM)是一种罕见的炎症性疾病,多见于育龄妇女。虽然IGM具有良性的性质,但它可以模拟广泛的疾病,并可能导致错误的癌症诊断。此外,患者通常经历一个漫长的病程,这是令人痛苦的。但IGM的临床病理表现不明确,不具有特异性。目的:本研究旨在评估IGM的临床病理方面。方法:对2010年至2019年在伊朗德黑兰Shohada-e-Tajrish医院初步诊断为IGM的20 - 50岁患者进行横断面回顾性研究。然后,对入组患者的人口统计学、临床、超声和组织病理学特征进行评估。结果:本研究共纳入60名年龄在20 - 50岁之间且最初诊断为IGM的女性。平均年龄34.5±6.73岁。在所有参与者中,38.3%的患者有乳腺癌家族史。病变最常见的部位为上外象限(UOQ),以左侧为主(36.6%)。她们更有可能出现乳房疼痛、红斑、肿胀和发热(51.6%),其次是可触及的肿块(38.3%)。超声检查结果显示43.3%的患者为管状低回声肿块,其余患者为肿瘤样病变(21.6%)和脓肿形成(15%)。组织学上,非干酪化肉芽肿伴混合炎症细胞(70%)和被中性粒细胞聚集包围的囊性空腔形成(15%)是主要特征。结论:尽管罕见的疾病,IGM是一个诊断挑战,因为它可以伪装各种乳腺疾病。明确的诊断需要临床、放射学和组织病理学结果的合作。
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
67
期刊介绍: International Journal of Cancer Management (IJCM) publishes peer-reviewed original studies and reviews on cancer etiology, epidemiology and risk factors, novel approach to cancer management including prevention, diagnosis, surgery, radiotherapy, medical oncology, and issues regarding cancer survivorship and palliative care. The scope spans the spectrum of cancer research from the laboratory to the clinic, with special emphasis on translational cancer research that bridge the laboratory and clinic. We also consider original case reports that expand clinical cancer knowledge and convey important best practice messages.
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