Thomas T M, Myint A, Mak C K, Chan J K
Department of Pathology, Kwong Wah Hospital, Hong Kong.
Am J Clin Pathol. 1997 Jan;107(1):52-5. doi: 10.1093/ajcp/107.1.52.
An unusual example of mammary myofibroblastoma in a 36-year-old woman was reported. The central portion resembled mammary myofibroblastoma or solitary fibrous tumor of other sites and showed reactivity for CD34 and muscle-specific actin, with few cells staining for desmin. The peripheral portion resembled leiomyoma and showed strong reactivity for actin and desmin but only focal staining for CD34. We interpret this tumor as mammary myofibroblastoma showing frank peripheral leiomyomatous differentiation. Although closely related to solitary fibrous tumor, mammary myofibroblastoma appears slightly different because of its consistent slant toward myoid differentiation in the form of actin and variable desmin reactivity as opposed to the rare and sparse immunohistochemical expression of myoid features by solitary fibrous tumors of other sites. This case demonstrates this phenomenon carried to an extreme, a feature not previously documented in mammary myofibroblastoma. It is of interest to note the modulation of the antigenic profile with the differentiation process, that is, loss of CD34 and gain of desmin accompanying the myoid differentiation.
报道了一例36岁女性乳腺肌纤维母细胞瘤的罕见病例。肿瘤中央部分类似乳腺肌纤维母细胞瘤或其他部位的孤立性纤维瘤,CD34和肌特异性肌动蛋白呈阳性反应,仅少数细胞结蛋白染色阳性。外周部分类似平滑肌瘤,肌动蛋白和结蛋白呈强阳性反应,但CD34仅局灶性染色。我们将此肿瘤解释为显示明显外周平滑肌瘤样分化的乳腺肌纤维母细胞瘤。尽管乳腺肌纤维母细胞瘤与孤立性纤维瘤密切相关,但由于其始终倾向于以肌动蛋白形式出现的肌样分化以及结蛋白反应性可变,而其他部位的孤立性纤维瘤肌样特征的免疫组化表达罕见且稀少,因此乳腺肌纤维母细胞瘤似乎略有不同。该病例展示了这一现象的极端情况,这一特征此前在乳腺肌纤维母细胞瘤中未见报道。值得注意的是,随着分化过程抗原谱的变化,即随着肌样分化CD34丢失而结蛋白增加。