Fritzsche Florian Rudolf, Pahl Stefan, Petersen Iver, Burkhardt Mick, Dankof Anja, Dietel Manfred, Kristiansen Glen
Institute of Pathology, Charité Universitätsmedizin Berlin, Schumannstr. 20/21, 10117 Berlin, Germany.
Virchows Arch. 2006 Nov;449(5):561-4. doi: 10.1007/s00428-006-0287-1. Epub 2006 Sep 16.
Primary, as well as secondary, lymphomas of the breast are rare diseases and might, in some cases, be misdiagnosed as breast cancer on routine hematoxylin/eosin stainings. We report a case of an anaplastic large cell lymphoma in a 72-year-old woman with a history of breast cancer treated with breast-ablative surgery and a subsequent silicon implant 32 years ago. Clinically, she presented with an ulceration of the skin, which had developed within a few months. On conventional histology, the tumor cells were mimicking poorly differentiated invasive ductal carcinoma with a prominent leukocytic infiltrate. The immunoprofile of the tumor showed negativity for cytokeratins and led to the diagnosis of a CD30-positive anaplastic large cell lymphoma.
原发性以及继发性乳腺淋巴瘤均为罕见疾病,在某些情况下,常规苏木精/伊红染色可能会将其误诊为乳腺癌。我们报告一例72岁女性的间变性大细胞淋巴瘤病例,该患者32年前有乳腺癌病史,接受了乳房切除手术并随后植入了硅胶假体。临床上,她出现了皮肤溃疡,在几个月内形成。在传统组织学检查中,肿瘤细胞类似低分化浸润性导管癌,伴有明显的白细胞浸润。肿瘤的免疫表型显示细胞角蛋白阴性,从而诊断为CD30阳性间变性大细胞淋巴瘤。