Seidal T, Kindblom L G, Angervall L
Department of Pathology, Sahlgren Hospital, Göteborg, Sweden.
Appl Pathol. 1987;5(4):201-19.
The present study is an immunohistochemical analysis utilizing a series of mono- and polyclonal antibodies to myoglobin, desmin and vimentin in smooth and striated control muscle tissues, 7 alveolar and 7 embryonal rhabdomyosarcomas and 1 adult and 1 fetal rhabdomyoma with ultrastructurally proven rhabdomyoblastic differentiation in all the tumors. Formaldehyde-fixed and paraffin-embedded tissue was used for the immunohistochemical analysis of all the tumors, while ethanol fixation was also used for the analysis of the control tissues. The staining for myoglobin with the poly- and monoclonal antibody used was positive in both formaldehyde- and ethanol-fixed skeletal and cardiac control muscle. Trypsin treatment abolished the positive staining when the monoclonal antibody was used. Both the striated and smooth control muscle tissues were positively stained by the antidesmin antibodies. The influence of the fixative that was used and the trypsin treatment depended on the antibody used and the type and origin of the muscle tissue. All the tumors were positively stained with the polyclonal antimyoglobin and 8/14 rhabdomyosarcomas and the 2 rhabdomyomas were positively stained with the monoclonal antimyoglobin. All the tumors were positively stained with the polyclonal and 3 of the 5 monoclonal antidesmin antibodies used. Well-differentiated tumor cells were usually positively stained for both myoglobin and desmin. There were small, poorly differentiated tumor cells in the rhabdomyosarcomas and the fetal rhabdomyoma which were positively stained for desmin, whereas very few or no such cells were positively stained for myoglobin. A varying number of mostly small, poorly differentiated tumor cells were positively stained for vimentin in 12 of 14 rhabdomyosarcomas and in the fetal rhabdomyoma. The study showed that one of the monoclonal antidesmin antibodies produced the most consistent result with a positive staining in all cases. The monoclonal antimyoglobin antibody, which is a specific marker of rhabdomyoblastic differentiation, is also considered to be of value, although it did not produce positivity in all cases. It remains to be shown whether desmin can help in the diagnosis of poorly or undifferentiated rhabdomyosarcomas without light- or electron-microscopic evidence of rhabdomyoblastic differentiation.
本研究是一项免疫组织化学分析,使用了一系列针对肌红蛋白、结蛋白和波形蛋白的单克隆及多克隆抗体,对平滑肌和横纹肌对照组织、7例肺泡型和7例胚胎型横纹肌肉瘤以及1例成人横纹肌瘤和1例胎儿横纹肌瘤进行检测,所有肿瘤均经超微结构证实具有横纹肌母细胞分化。所有肿瘤均采用甲醛固定、石蜡包埋组织进行免疫组织化学分析,对照组织则同时采用乙醇固定进行分析。所使用的多克隆和单克隆抗体对肌红蛋白的染色在甲醛固定和乙醇固定的骨骼肌及心肌对照组织中均呈阳性。使用单克隆抗体时,胰蛋白酶处理可消除阳性染色。抗结蛋白抗体对横纹肌和平滑肌对照组织均呈阳性染色。所使用的固定剂和胰蛋白酶处理的影响取决于所使用的抗体以及肌肉组织的类型和来源。所有肿瘤用多克隆抗肌红蛋白抗体染色均呈阳性,8/14例横纹肌肉瘤和2例横纹肌瘤用单克隆抗肌红蛋白抗体染色呈阳性。所有肿瘤用所使用的多克隆和5种单克隆抗结蛋白抗体中的3种染色均呈阳性。分化良好的肿瘤细胞通常肌红蛋白和结蛋白染色均呈阳性。横纹肌肉瘤和胎儿横纹肌瘤中有小的、分化差的肿瘤细胞,结蛋白染色呈阳性,而肌红蛋白染色呈阳性的此类细胞极少或没有。14例横纹肌肉瘤中的12例以及胎儿横纹肌瘤中有数量不等的大多为小的、分化差的肿瘤细胞波形蛋白染色呈阳性。研究表明,所产生的一种单克隆抗结蛋白抗体在所有病例中染色结果最一致且呈阳性。单克隆抗肌红蛋白抗体作为横纹肌母细胞分化的特异性标志物,尽管并非在所有病例中都呈阳性,但也被认为具有价值。在没有光镜或电镜下横纹肌母细胞分化证据的情况下,结蛋白是否有助于诊断低分化或未分化横纹肌肉瘤仍有待证实。