Cintorino M, Vindigni C, Del Vecchio M T, Tosi P, Frezzotti R, Hadjistilianou T, Leoncini P, Silvestri S, Skalli O, Gabbiani G
Department of Pathology, University of Siena, Italy.
J Submicrosc Cytol Pathol. 1989 Jul;21(3):409-19.
The diagnosis of orbital rhabdomyosarcoma (RMS) in childhood gives rise to several clinical and anatomo-pathological problems. Antibodies recognizing structural proteins and cytoskeletal components have been shown to increase the diagnostic accuracy of different neoplastic lesions. In this study we examined anatomo-clinically and, where possible, by means of immunohistochemistry and electron microscopy, a series of 14 cases of orbital RMS in childhood. In the 12 cases studied by immunohistochemistry, desmin was always present, although showing variable patterns, and alpha-sarcomeric actin was found in 10 cases. alpha-Smooth muscle actin was always absent. The other markers tested (myoglobin, polyclonal actin, vimentin and enolase) proved unreliable for several reasons. We conclude that antibodies against desmin and alpha-sarcomeric actin are useful for the diagnostic definition of RMS. In addition, immunohistochemical analysis supplies data regarding the degree of tumor differentiation and may be applied to monitor radio- and chemotherapy.
儿童眼眶横纹肌肉瘤(RMS)的诊断引发了若干临床和解剖病理学问题。已证实,识别结构蛋白和细胞骨架成分的抗体可提高不同肿瘤性病变的诊断准确性。在本研究中,我们对一系列14例儿童眼眶RMS进行了临床解剖学检查,并尽可能通过免疫组织化学和电子显微镜进行检查。在通过免疫组织化学研究的12例病例中,结蛋白始终存在,尽管表现出不同的模式,并且在10例病例中发现了α-肌节肌动蛋白。α-平滑肌肌动蛋白始终不存在。由于多种原因,所测试的其他标志物(肌红蛋白、多克隆肌动蛋白、波形蛋白和烯醇化酶)被证明不可靠。我们得出结论,抗结蛋白和α-肌节肌动蛋白的抗体对RMS的诊断定义有用。此外,免疫组织化学分析提供了有关肿瘤分化程度的数据,可用于监测放疗和化疗。