Hiraoka N, Mukai M, Hosoda Y, Hata J
Department of Pathology, Keio University School of Medicine, Tokyo, Japan.
Am J Surg Pathol. 1994 May;18(5):506-11. doi: 10.1097/00000478-199405000-00011.
This report illustrates a case of the phyllodes tumor of the breast with intracytoplasmic inclusion bodies that are diffusely distributed over the tumor. The inclusion bodies were identified as aggregated actin filaments by modified immunohistochemical and ultrastructural analyses. These structures are thought to be identical to those of the characteristic intracytoplasmic inclusion bodies observed in the case of infantile digital fibromatosis. To date, tumors with such intracytoplasmic inclusion bodies have been recognized exclusively as infantile digital fibromatosis. Although a few rare cases in which the infantile digital fibromatosis-like tumor occurred outside the digit or in adulthood, all these cases were in the category of fibromatosis or fibroma. This case is the first instance of the tumor containing intracytoplasmic inclusion bodies identical with the infantile digital fibromatosis other than fibromatosis or fibroma.
本报告展示了一例乳腺叶状肿瘤,其胞质内包涵体弥漫分布于肿瘤中。通过改良的免疫组织化学和超微结构分析,这些包涵体被鉴定为聚集的肌动蛋白丝。这些结构被认为与婴儿指纤维瘤病病例中观察到的特征性胞质内包涵体相同。迄今为止,具有这种胞质内包涵体的肿瘤仅被认为是婴儿指纤维瘤病。尽管有少数罕见病例,其中婴儿指纤维瘤病样肿瘤发生在手指以外或成年期,但所有这些病例都属于纤维瘤病或纤维瘤类别。本病例是除纤维瘤病或纤维瘤外,首次出现含有与婴儿指纤维瘤病相同胞质内包涵体的肿瘤。