肉芽肿性乳腺炎:临床和诊断的困境。

IF 1.1 Q4 PATHOLOGY
Emel Ebru Pala, Sumeyye Ekmekci, Melis Kilic, Ayberk Dursun, Gul Colakoglu, Cem Karaali, Mumin Emiroglu, Mustafa Emiroglu
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引用次数: 6

摘要

目的:肉芽肿性乳腺炎(GM)是一种具有挑战性的乳腺炎性疾病。在这项研究中,我们旨在介绍GM病例的详细临床和形态学特征,特定和特发性病因的诊断线索,评估肿瘤活检的困难,以及不同治疗方法的结果。材料和方法:我们回顾性分析114例经细针穿刺诊断的GM病例的临床、放射学和形态学特征。结果:平均年龄35.8岁。年龄在45岁以上的只有8例。双侧受累4例(3.5%)。最常见的临床症状是乳房肿块/脓肿、压痛和皮肤变化。微生物培养革兰氏阳性菌4例。仅有3例结核杆菌素/PCR检测阳性。USG的主要发现是低回声、清晰或不明确的肿块/脓肿;MRI表现为非肿块增强。细胞学诊断的病例(35例)在病史或临床随访期间均无乳腺恶性肿瘤。细针吸细胞学检查显示上皮肉芽肿伴中性粒细胞,淋巴细胞伴巨细胞,化脓性坏死。对65例肿瘤活检进行组织病理学重新评估,发现肉芽肿65例(100%),朗汉斯巨细胞59例(90.7%),微脓肿41例(63%),干酪样坏死1例(1.5%),嗜中性粒细胞囊肿30例(46.1%),嗜酸性粒细胞浸润48例(73.8%),小叶间炎症14例(21.5%),脂肪坏死5例(7.6%),导管扩张6例(9.2%),泌乳改变4例(6.1%)。肉芽肿以小叶为中心58例,异物型/脂肪坏死相关6例,管周1例。囊性中性粒细胞肉芽肿性乳腺炎1例。我们还评估了这65例活检的组织化学染色。EZN法检测耐酸杆菌阳性1例,革兰氏染色检测革兰氏阳性杆菌阳性1例。结论:肉芽肿性乳腺炎的小的、浅表的组织活检可能给确定病因和鉴别诊断带来困难。对于最佳的管理和适当的治疗时机,理想的活检程序,特殊的染色,以及由外科医生,病理学家和放射科医生组成的多学科团队是最重要的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Granulomatous Mastitis: A Clinical and Diagnostic Dilemma.

Granulomatous Mastitis: A Clinical and Diagnostic Dilemma.

Granulomatous Mastitis: A Clinical and Diagnostic Dilemma.

Granulomatous Mastitis: A Clinical and Diagnostic Dilemma.

Objective: Granulomatous mastitis (GM) is a challenging inflammatory disorder of the breast. In this study we aimed to present the detailed clinical and morphological features of GM cases, diagnostic clues for specific and idiopathic etiologies, the difficulties in evaluating trucut biopsies, and the results of different therapeutic approaches.

Material and method: We retrospectively analysed the clinical, radiological and morphological features of 114 GM cases diagnosed with fine needle aspiration, and trucut, incisional, and excisional biopsy.

Results: The mean age was 35.8. Only eight cases were older than 45 years. Bilateral involvement was observed in 4 (3.5%) cases. The most common clinical symptoms were breast mass/abscesses, tenderness, and skin changes. Microbiological culture was positive in 4 cases for gram-positive bacteria. Only 3 cases showed a positive tuberculin/PCR test for tuberculosis. The major USG finding was a hypoechoic well-defined or ill-defined mass/abscess; MRI finding was heterogeneous non-mass contrast enhancement. Cases diagnosed with cytology (35 cases) did not have breast malignancy either in their history or clinical follow up period. Fine needle aspiration cytology materials revealed epitheloid granulomas mixed with neutrophils, lymphocytes accompanied by giant cells, and suppurative necrosis. Histopathological reevaluation of 65 trucut/incisional/ excisional biopsies revealed granuloma formation in 65 (100%), Langhans type giant cells in 59 (90.7%), microabscess formation in 41 (63%), caseous necrosis in 1 (1.5%), neutrophilic cysts in 30 (46.1%), eosinophilic infiltration in 48 (73.8%), interlobular inflammation in 14 (21.5%), fat necrosis in 5 (7.6%), ductal ectasia in 6 (9.2%), and lactational changes in 4 (6.1%) cases. Granulomas were lobulocentric in 58 cases, foreign body type/fat necrosis-related in 6 case, and periductular in 1 case. Cystic neutrophilic granulomatous mastitis was observed in one case. We also evaluated the histochemical stains of these 65 biopsies. Only one sample was positive for acido-resistant bacilli (ARB) by the EZN method and one sample was positive for gram-positive bacilli by gram stain.

Conclusion: Small, superficial trucut biopsies may cause difficulties in determining the etiology and differential diagnosis of granulomatous mastitis. For optimal management and timing the appropriate therapy, the ideal biopsy procedure, special stains, and a multidisciplinary team consisting of the surgeon, pathologist, and radiologist are the most important issues.

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来源期刊
CiteScore
1.90
自引率
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