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Malignant transformation in craniopharyngioma after radiation therapy: a case report and review of the literature.

机译:放射治疗后颅咽管瘤的恶性转化:1例病例并文献复习。

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OBJECTIVE: Craniopharyngioma is a benign epithelial tumor that is thought to arise from the remnant of the Rathke pouch. Malignant transformation in craniopharyngioma is extremely rare. Herein, we report a case of malignant transformation in craniopharyngioma after radiation therapy. MATERIALS AND METHODS: Histopathological and immunohistochemical analyses were carried out for specimens of the suprasellar tumor (from three resections, with the third surgery performed after radiation therapy). RESULTS: The resected tumors from the first and second surgeries comprised islands of loosely cohesive aggregates of epithelial cells, so-called stellate reticulum. At the periphery of the nests, palisaded columnar epithelium was observed. Wet keratins were scattered, and few mitotic figures were seen. The third surgical specimen was composed of irregular large nests of basaloid cells that had large, round to oval nuclei with prominent nucleoli, and mitotic figures were frequently seen (21/10 high power fields). In the center of the nests, eosinophilic ghost cells, resembling wet keratin, were observed. Accordingly, the diagnosis of malignant transformation in craniopharyngioma was made. Immunohistochemical studies revealed that the p53 protein was over-expressed in the malignant component, whereas its expression was much lower in the benign component. CONCLUSIONS: Similar to the ten previously reported cases of malignant transformation in craniopharyngioma, the present case occurred after radiation therapy. p53 protein overexpression was also observed in the earlier cases of malignant craniopharyngioma as well as in the present case (6/6 cases). We concluded that radiation therapy and p53 mutations could be involved in malignant transformation in craniopharyngioma.
机译:目的:颅咽管瘤是一种良性上皮性肿瘤,被认为是由Rathke囊的残余引起的。颅咽管瘤的恶性转化极为罕见。在此,我们报道了放疗后颅咽管瘤的恶变。材料与方法:对鞍上肿瘤标本进行了组织病理学和免疫组化分析(来自三个切除,放射治疗后进行了第三次手术)。结果:第一次和第二次手术切除的肿瘤包括上皮细胞疏松凝聚的聚集体岛,即所谓的星状网状组织。在巢的外围,观察到栅栏状的柱状上皮。湿的角蛋白散在,几乎看不到有丝分裂的数字。第三个外科手术标本由基底细胞的不规则大巢组成,基底细胞具有从核仁突出的大的,圆形到椭圆形的核,并且经常看到有丝分裂图(21/10高倍视野)。在巢的中心,观察到嗜酸性的鬼细胞,类似于湿的角蛋白。因此,诊断为颅咽管瘤的恶性转化。免疫组织化学研究表明,p53蛋白在恶性成分中过表达,而其表达在良性成分中低得多。结论:与先前报道的十例颅咽管瘤恶性转化病例相似,本病例发生在放射治疗后。在较早的恶性颅咽管瘤病例和本病例(6/6例)中也观察到了p53蛋白的过表达。我们得出的结论是,放射治疗和p53突变可能与颅咽管瘤的恶性转化有关。

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