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乳腺包涵体性纤维瘤病。两例的免疫组化和超微结构研究结果

Inclusion body fibromatosis of the breast. Two cases with immunohistochemical and ultrastructural findings.

作者信息

Pettinato G, Manivel J C, Gould E W, Albores-Saavedra J

机构信息

Department of Pathology, University of Naples Federico II, Italy.

出版信息

Am J Clin Pathol. 1994 Jun;101(6):714-8. doi: 10.1093/ajcp/101.6.714.

DOI:10.1093/ajcp/101.6.714
PMID:8209857
Abstract

Two cases of fibromatosis of the breast, characterized by a proliferation of spindle cells containing intracytoplasmic, spherical, eosinophilic inclusion bodies, are reported. The light and electron microscopic features, as well as the immunohistochemical features, are indistinguishable from those found in infantile digital fibromatosis. The proliferating spindle cells are characterized as myofibroblasts, whereas the inclusion bodies show an immunohistochemically nonreactive, hollow-like pattern with peripheral reactivity for actin filaments. This lesion, observed for the first time in the breast, expands the number of extradigital inclusion body fibromatoses.

摘要

本文报告了两例乳腺纤维瘤病,其特征为含有胞浆内球形嗜酸性包涵体的梭形细胞增生。光镜、电镜及免疫组化特征与婴儿指部纤维瘤病所见难以区分。增生的梭形细胞被鉴定为肌成纤维细胞,而包涵体显示免疫组化无反应性的中空样模式,周边有肌动蛋白丝反应性。此病变首次在乳腺中观察到,增加了指外包涵体纤维瘤病的病例数。

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Inclusion body fibromatosis of the breast. Two cases with immunohistochemical and ultrastructural findings.乳腺包涵体性纤维瘤病。两例的免疫组化和超微结构研究结果
Am J Clin Pathol. 1994 Jun;101(6):714-8. doi: 10.1093/ajcp/101.6.714.
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引用本文的文献

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Congenital infantile digital fibromatosis: a case report and review of the literature.先天性婴儿指纤维瘤病:一例病例报告及文献复习
Afr Health Sci. 2020 Dec;20(4):1865-1869. doi: 10.4314/ahs.v20i4.42.
2
Infantile digital fibromatosis (inclusion body fibromatosis) observed in a baby without finger involvement.婴儿指部纤维瘤病(包涵体纤维瘤病),见于一名未累及手指的婴儿。
Indian J Dermatol. 2013 Mar;58(2):160. doi: 10.4103/0019-5154.108085.