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儿童横纹肌肉瘤。肌红蛋白、结蛋白和波形蛋白的免疫组织学分析。

Rhabdomyosarcoma in childhood. An immunohistological analysis with myoglobin, desmin and vimentin.

作者信息

Kodet R

机构信息

Department of Pathology, Faculty of Pediatric Medicine, Charles' University, Prague, CSSR.

出版信息

Pathol Res Pract. 1989 Aug;185(2):207-13. doi: 10.1016/S0344-0338(89)80253-5.

Abstract

A retrospective immunohistological analysis of 64 rhabdomyosarcomas in children was performed using antibodies against desmin and in 35 cases against myoglobin. In addition a group of 12 undifferentiated tumours in which the differential diagnosis included rhabdomyosarcomas was studied. Rhabdomyosarcomas were desmin positive in 57 cases (89%), 28 cases of which showed positivity of undifferentiated small cells (44%). Myoglobin was positive in 23 cases (66%), but only one case showed positivity of undifferentiated small cells. The results show the limited use of myoglobin in the diagnosis of rhabdomyosarcoma, especially of cases with a low degree of differentiation. Three out of 12 undifferentiated tumours were desmin positive and were reclassified as rhabdomyosarcomas. In 49 rhabdomyosarcomas the investigation was complemented by the demonstration of vimentin. Vimentin was shown to be present in 27 cases in tumour cells (55%). Undifferentiated cells were positive in 26 tumours (53%) and rhabdomyoblasts reacted in 9 cases (18%). Coexpression of vimentin and desmin in some cases reflects a situation in rhabdomyosarcomas that aberrantly mimics skeletal muscle embryogenesis. In three cases desmin and vimentin positive globular inclusions were observed. It is suggested that their formation is related to dystrophic changes of contractile and cytoskeletal filaments. From the diagnostic point of view a high percentage of desmin positive cases makes desmin a successful marker for rhabdomyoblastic tumours. It is pointed out, however, that even immunohistochemistry may not contribute to solving the problem of undifferentiated tumours and that each case must be evaluated comprehensively.

摘要

对64例儿童横纹肌肉瘤进行了回顾性免疫组织学分析,使用抗结蛋白抗体检测,35例还使用了抗肌红蛋白抗体检测。此外,对一组12例未分化肿瘤进行了研究,其鉴别诊断包括横纹肌肉瘤。横纹肌肉瘤中57例(89%)结蛋白呈阳性,其中28例(44%)未分化小细胞呈阳性。肌红蛋白23例(66%)呈阳性,但仅1例未分化小细胞呈阳性。结果表明肌红蛋白在横纹肌肉瘤诊断中的应用有限,尤其是在低分化病例中。12例未分化肿瘤中有3例结蛋白呈阳性,重新分类为横纹肌肉瘤。对49例横纹肌肉瘤进行波形蛋白检测作为补充。结果显示27例(55%)肿瘤细胞中存在波形蛋白。26例(53%)未分化细胞呈阳性,9例(18%)成肌细胞呈阳性。波形蛋白和结蛋白在某些病例中的共表达反映了横纹肌肉瘤中异常模拟骨骼肌胚胎发生的情况。3例观察到结蛋白和波形蛋白阳性的球状包涵体。提示其形成与收缩和细胞骨架细丝的营养不良性改变有关。从诊断角度看,结蛋白阳性病例比例高,使其成为成肌细胞瘤的成功标志物。然而,需要指出的是,即使免疫组织化学也可能无助于解决未分化肿瘤的问题,每个病例都必须进行全面评估。

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