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Idiopathic granulomatous mastitis - a new approach in diagnostics and treatment

机译:特发性肉芽肿的乳腺炎 - 一种诊断与治疗的新方法

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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; followed by a statistical evaluation. 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.
机译:特发性肉芽肿乳腺炎(IgM)是一种稀有的炎症性乳腺疾病,模仿癌和呕吐物或非赋乳腺炎。该前瞻性表现对照研究的主要目的是将IgM的临床和成像与非特异性非赋乳腺炎(NM)的参考组进行比较,以确定对正确鉴别诊断的最典型的临床和成像标志。次要目的是提出一种新的非侵入性治疗方法。组织学证明IGM和二十六名患有非特异性乳腺炎的二十九名妇女接受临床检查,乳房超声(美国),乳房X线照相术(MG)和MRI检查。为每个组和方法选择最典型的迹象;其次是统计评估。通过临床检查和成像评估了秋水仙碱,维生素E和Ribwort植物酊治疗的效果。 IGM的典型临床迹象包括单侧急性发作的乳腺水肿,发红,可触及的肿块,缺失发烧,淋巴结病,对抗生素或外科干预不反应。超声波透露:“指状”结构(100%),再生联酶(76.9%),脓肿(76.9%)和淋巴结病(15.4%),而在MRI皮肤和组织水肿(100%),多元病灶(100%) ,脓肿(76.9%),环增强(84.6%),淋巴结病(15.4%)和小增强淋巴结(38.5%)。在IgM的患者中,临床症状,瘘管,低压杂种物质,DWISECTASIAS和扩散加权图像(DWI)限制显着更频繁频繁。根据疾病程度,治疗效果在6-19个月之间完全反应,得到了100%。有针对性的问题与成像一起加速选择,以便使用血清曲霉,维生素E和局部治疗进行适当的治疗方法。应避免持久使用抗生素和反复外科干预措施。

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