Yan Mingfei, Bomeisl Phillip, Gilmore Hannah, Sieck Leah, Kuchta Zachariah, Harbhajanka Aparna
Department of Pathology, University Hospitals Cleveland Medical Center, Cleveland, OH, USA; Case Western Reserve University, Cleveland, OH, USA.
Department of Pathology, University Hospitals Cleveland Medical Center, Cleveland, OH, USA; Case Western Reserve University, Cleveland, OH, USA.
Ann Diagn Pathol. 2020 Oct;48:151591. doi: 10.1016/j.anndiagpath.2020.151591. Epub 2020 Aug 15.
Myofibroblastoma is a rare type of benign myofibroblastic neoplasm in the breast. It is clinically presented as a well-circumscribed mass, usually small in size (usually less than 4.0 cm), and can mostly be cured by local excision. Rare cases of giant myofibroblastoma greater than 10 cm have been reported, but also follow a benign clinical course. Histologically, breast myofibroblastoma is featured by bland fascicles of spindle cells intermixed with thick hyalinized collagen bundles. Mast cells are frequently found within the stroma. However, a wide spectrum of morphological variants can occur in myofibroblatoma, making its diagnosis challenging sometimes. Differential diagnosis of myofibroblastoma with other spindle cell lesions in the breast, either benign or malignant, is also important in practice. In this study, we collected 15 cases of breast myofibroblastoma diagnosed in our institution during a 20 year period. The sizes of these cases range from 0.4 cm to 35.2 cm (mean is 3.7 cm). To our knowledge, the case of giant breast myofibroblastoma we presented here is the largest one reported to date. The histological examination of the cases show great morphological variations. Besides the classical type, features of cellular, collagenized, palisading, epithelioid, myxoid, myoid, solitary fibrous tumor-like are also identified in the case series. Immunohistochemical staining patterns as well as clinical features of the cases are also summarized and compared. All cases in this study show no recurrence on follow-up. In addition, cases that are important differential diagnosis for breast myofibroblastoma are also studied. Their key histological characteristics are compared with myofibroblastoma, and their immunohistochemical and molecular features are discussed.
肌纤维母细胞瘤是乳腺中一种罕见的良性肌纤维母细胞性肿瘤。临床上表现为边界清楚的肿块,通常体积较小(通常小于4.0厘米),大多可通过局部切除治愈。有报道称罕见的巨大肌纤维母细胞瘤(大于10厘米),但其临床过程也为良性。组织学上,乳腺肌纤维母细胞瘤的特征是梭形细胞呈温和的束状排列,夹杂着粗大的玻璃样变胶原束。间质中常可见肥大细胞。然而,肌纤维母细胞瘤可出现多种形态学变异,有时使其诊断具有挑战性。在实践中,将肌纤维母细胞瘤与乳腺其他梭形细胞病变(良性或恶性)进行鉴别诊断也很重要。在本研究中,我们收集了本机构在20年期间诊断的15例乳腺肌纤维母细胞瘤病例。这些病例的大小从0.4厘米到35.2厘米不等(平均为3.7厘米)。据我们所知,我们在此呈现的巨大乳腺肌纤维母细胞瘤病例是迄今为止报道的最大病例。这些病例的组织学检查显示出很大的形态学差异。除了经典类型外,在病例系列中还发现了细胞型、胶原化型、栅栏状型、上皮样型、黏液样型、肌样型、孤立性纤维瘤样型等特征。还总结并比较了这些病例的免疫组化染色模式以及临床特征。本研究中的所有病例随访均无复发。此外,还研究了对乳腺肌纤维母细胞瘤重要的鉴别诊断病例。将它们的关键组织学特征与肌纤维母细胞瘤进行了比较,并讨论了它们的免疫组化和分子特征。