Zámecník M, Michal M, Simpson R H, Lamovec J, Hlavcák P, Kinkor Z, Mukensnábl P, Matĕjovský Z, Betlach J
Department of Pathology, Postgraduate Medical School, Bratislava, Slovak Republic.
Ann Diagn Pathol. 1997 Dec;1(2):73-81. doi: 10.1016/s1092-9134(97)80011-1.
Ossifying fibromyxoid tumor of soft parts is an unusual benign neoplasm, with a tendency for local recurrence. Its typical microscopic appearance is that of a multinodular proliferation of round to spindle shaped cells separated by fibrous bands in which bone formation is often seen. Herein, we present the clinicopathologic features of 17 examples of this tumor with particular emphasis on some unusual histopathologic features that may place pitfalls in the diagnosis of this tumor, including satellite micronodules, mucinous microcysts, absence of myxoid areas, crush artifact, multiple microcalcifications, epidermoid cysts, atypical chondroid differentiation with binucleate lacunar cells, pericytic growth pattern, and malignant change. Awareness of these unusual morphologic features should lead to a search for areas displaying the more typical features of ossifying fibromyxoid tumor to arrive at a correct diagnosis.
软组织骨化性纤维黏液样肿瘤是一种罕见的良性肿瘤,有局部复发倾向。其典型的镜下表现为圆形至梭形细胞呈多结节状增生,被纤维带分隔,纤维带中常可见骨形成。在此,我们呈现17例该肿瘤的临床病理特征,特别强调一些可能在该肿瘤诊断中造成误诊的不寻常组织病理学特征,包括卫星微结节、黏液性微囊肿、无黏液样区域、挤压假象、多发微钙化、表皮样囊肿、具有双核陷窝细胞的非典型软骨样分化、周细胞生长模式以及恶变。认识到这些不寻常的形态学特征应促使寻找显示骨化性纤维黏液样肿瘤更典型特征的区域,以得出正确诊断。