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乳腺栅栏状肌纤维母细胞瘤:一种酷似神经鞘瘤的肿瘤:2 例报告。

Palisaded myofibroblastoma of the breast: a tumor closely mimicking schwannoma: Report of 2 cases.

机构信息

Department G.F. Ingrassia, Azienda Ospedaliero-Universitaria Policlinico-Vittorio Emanuele Anatomic Pathology, University of Catania, 95123 Catania, Italy.

出版信息

Hum Pathol. 2013 Sep;44(9):1941-6. doi: 10.1016/j.humpath.2013.01.018. Epub 2013 Apr 8.

Abstract

Myofibroblastoma is a relatively rare, benign mesenchymal tumor that typically occurs in the breast parenchyma. Unlike mammary-type myofibroblastoma, myofibroblastoma that primarily arises in the lymph nodes exhibits nuclear palisading, and the term palisaded myofibroblastoma has been proposed, accordingly. We report 2 unusual cases of myofibroblastoma of the male breast, which showed a predominant (>90% of the entire tumor) nuclear palisading and Verocay-like bodies. The present cases represent a hitherto unreported variant of mammary-type myofibroblastoma closely mimicking schwannoma. The diagnosis of myofibroblastoma was supported by immunohistochemical analyses showing a diffuse staining for desmin and CD34. In addition, the diagnosis of myofibroblastoma was confirmed in 1 case cytogenetically by the demonstration of the monoallelic loss of the FOXO1/13q14 locus by fluorescence in situ hybridization. Pathologists should be aware of this unusual variant of mammary myofibroblastoma to assure a correct diagnosis.

摘要

肌纤维母细胞瘤是一种相对罕见的良性间叶性肿瘤,通常发生在乳腺实质中。与乳腺型肌纤维母细胞瘤不同,主要发生在淋巴结的肌纤维母细胞瘤表现为核栅状排列,因此提出了栅状肌纤维母细胞瘤这一术语。我们报告了 2 例男性乳腺肌纤维母细胞瘤的不典型病例,这些肿瘤表现为明显的(> 整个肿瘤的 90%)核栅状排列和 Verocay 样小体。目前这些病例代表了一种以前未报道的乳腺型肌纤维母细胞瘤变体,与神经鞘瘤非常相似。免疫组织化学分析显示弥漫性 desmin 和 CD34 染色支持肌纤维母细胞瘤的诊断。此外,通过荧光原位杂交显示 FOXO1/13q14 位点单等位基因缺失,在 1 例病例中通过细胞遗传学证实了肌纤维母细胞瘤的诊断。病理学家应该意识到这种不典型的乳腺肌纤维母细胞瘤变体,以确保正确诊断。

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