Nielsen B B
University Institute of Pathology, Kommunehospitalet, Aarhus, Denmark.
Histopathology. 1987 Dec;11(12):1259-75. doi: 10.1111/j.1365-2559.1987.tb01871.x.
Twenty-seven cases of palpable and/or tumour-forming adenosis in the female breast, called adenosis tumour, have been investigated. It is a rare lesion, which most often presents as a breast mass that clinically and histologically is sometimes misinterpreted as carcinoma. The majority of patients were under the age of 45 years. Grossly, most tumours were firm or elastic and showed a grey or greyish-white cut surface. Furthermore, seven (26%) were granular and nine (34%) were microcystic, whereas none showed chalky streaks. Microscopically, 20 cases were poorly circumscribed and seven cases were well circumscribed. In contradistinction to the often uniform growth pattern of tubular carcinoma, the adenosis tumours characteristically showed adenosis arranged in a mixture of eight different growth patterns. The most frequent and also most extensive growth pattern was classical sclerosing adenosis and the least frequent was tubular adenosis. Another conspicuous feature in adenosis tumours was patchy growth in contrast to the stellate configuration of tubular carcinoma which is the most likely differential diagnosis. Other findings separating adenosis tumours from carcinomas were microcysts (93%), apocrine metaplasia (63%), luminal histiocytes (52%) and pseudopapillomas, called glomeruloid structures (48%). Epithelial changes that could cause anxiety about malignancy were frequently found and comprised epithelial hyperplasia (44%), epithelial atypia (26%) and fat or nerve infiltration (30%). Three patients were subjected to unnecessary mastectomy because of incorrectly diagnosed adenosis tumours. Adenosis tumours and non-infiltrating carcinoma were found together in five cases, but their association is probably over represented due to selection. None of 18 pure adenosis tumours solely treated by excision had recurred at follow-up 1-9 years later (mean 3.75 years).
对27例女性乳腺中可触及和/或形成肿瘤的腺病(称为腺病瘤)进行了研究。这是一种罕见的病变,最常表现为乳腺肿块,在临床和组织学上有时会被误诊为癌。大多数患者年龄在45岁以下。大体上,大多数肿瘤质地硬或有弹性,切面呈灰色或灰白色。此外,7例(26%)为颗粒状,9例(34%)为微囊状,而无一例有白垩样条纹。显微镜下,20例边界不清,7例边界清楚。与管状癌通常均匀的生长模式不同,腺病瘤的特征是腺病以8种不同生长模式混合排列。最常见且最广泛的生长模式是经典的硬化性腺病,最不常见的是管状腺病。腺病瘤的另一个显著特征是呈斑片状生长,这与最可能的鉴别诊断——管状癌的星状结构形成对比。将腺病瘤与癌区分开来的其他发现包括微囊肿(93%)、大汗腺化生(63%)、管腔内组织细胞(52%)和假乳头状瘤(称为肾小球样结构,48%)。经常发现可引起恶性肿瘤担忧的上皮改变,包括上皮增生(44%)、上皮异型性(26%)和脂肪或神经浸润(30%)。3例患者因腺病瘤诊断错误而接受了不必要的乳房切除术。5例同时发现腺病瘤和非浸润性癌,但由于选择因素,它们的关联可能被高估了。18例仅接受切除治疗的单纯腺病瘤在1 - 9年(平均3.75年)的随访中均未复发。