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特发性肉芽肿性乳腺炎——一种新的诊断和治疗方法。

Idiopathic Granulomatous Mastitis - a new approach in diagnostics and treatment.

机构信息

2nd Radiology Department, Faculty of Medicine, Comenius University in Bratislava, Bratislava, Slovakia.

St. Elizabeth Cancer Institute, Bratislava, Slovakia.

出版信息

Neoplasma. 2019 Jul 23;66(4):661-668. doi: 10.4149/neo_2019_190201N100.

Abstract

Idiopathic granulomatous mastitis (IGM) is a rare inflammatory breast disease mimicking carcinoma and puerperal or non-puerperal mastitis. The primary purpose of this prospectively performed case control study was to compare clinical and imaging signs of IGM with the reference group of nonspecific, non- puerperal mastitis (NM) to identify the most typical clinical and imaging signs essential for a correct differential diagnosis. The secondary purpose was to present a new approach to non-invasive treatment. Thirty-nine women with histologically proven IGM and twenty-six patients with nonspecific mastitis underwent clinical examination, breast ultrasound (US), mammography (MG) and MRI examination. The most typical signs were selected for each group, and method and were statistically evaluated. The effectivity of colchicine, vitamin E and ribwort plantain tincture in treatment was assessed by clinical examination and imaging. Typical clinical signs of IGM included unilateral acute onset of breast edema, redness, palpable masses, missing fever, lymphadenopathy, no response to antibiotics or surgical interventions. Ultrasound revealed: "finger-like" structures (100%), ductectasias (76.9%), abscesses (76.9%), and lymphadenopathy (15.4%), while in MRI skin and tissue edema (100%), multicentric lesions (100%), abscesses (76.9%), ring enhancement (84.6%), lymphadenopathy (15.4%) and small enhancing lymph nodes (38.5%) were observed. Among the clinical signs, fistulas, hypoechoic mass, ductectasias and diffusion weighted images (DWI) restriction were significantly more frequent in patients with IGM than in those with NM. Treatment effectivity yielded 100% with a complete response between 6-19 months, depending on the disease extent. Targeted questions together with imaging can speed up selection for proper treatment with colchicine, vitamin E and local treatment. Long lasting use of antibiotics and repeated surgical interventions should be avoided.

摘要

特发性肉芽肿性乳腺炎(IGM)是一种罕见的炎性乳腺疾病,表现为癌性病变、产褥期或非产褥期乳腺炎,易误诊。本前瞻性病例对照研究旨在比较 IGM 与非特异性、非产褥期乳腺炎(NM)的临床和影像学表现,以确定对正确鉴别诊断至关重要的最典型的临床和影像学表现。次要目的是提出一种新的非侵入性治疗方法。39 例经组织学证实的 IGM 患者和 26 例非特异性乳腺炎患者接受了临床检查、乳腺超声(US)、乳房 X 线摄影(MG)和 MRI 检查。选择每个组的最典型的征象,然后进行统计学评估。通过临床检查和影像学评估来评估秋水仙碱、维生素 E 和筋骨草提取物在治疗中的效果。IGM 的典型临床特征包括单侧急性乳房肿胀、发红、可触及的肿块、无发热、无淋巴结病、对抗生素或手术干预无反应。超声显示:“手指状”结构(100%)、导管扩张(76.9%)、脓肿(76.9%)和淋巴结病(15.4%),而在 MRI 中皮肤和组织水肿(100%)、多中心病变(100%)、脓肿(76.9%)、环状强化(84.6%)、淋巴结病(15.4%)和小增强淋巴结(38.5%)。在临床征象中,瘘管、低回声肿块、导管扩张和弥散加权成像(DWI)受限在 IGM 患者中比 NM 患者更常见。根据疾病程度,治疗效果在 6-19 个月内完全缓解率为 100%。有针对性的问题加上影像学检查可以加快选择秋水仙碱、维生素 E 和局部治疗的适当治疗。应避免长期使用抗生素和反复手术干预。

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