de Tella Oswaldo Ignácio, Herculano Marco Antonio, Prandini Mirto Nelso, Stavale João Norberto, Aguiar Paulo Henrique
Department of Neurosurgery, Federal University of São Paulo, Brazil.
Arq Neuropsiquiatr. 2003 Mar;61(1):104-6. doi: 10.1590/s0004-282x2003000100020. Epub 2003 Apr 16.
We report a case of a pleomorphic xantoastrocytoma which manifested itself as a cystic isodense lesion in the right fronto-temporal lobe in a 26 year-old woman. It appeared as a soft yellow tumor with cystic cavities on surgery. Five months after this surgery, the patient was submitted to a new operation, which revealed a friable tumor, easily differentiated from the normal parenchyma, with cystic components. The histopathological examination demonstrated pleomorphic xanthoastrocytoma with malignant transformation. Histologically, the tumor at first procedure was composed of pleomorphic astrocytes with multinucleated and foamy cells. A rare case of malignant transformation in pleomorphic xanthoastrocytoma is presented, discussed and illustrated in this paper.
我们报告了一例多形性黄色星形细胞瘤病例,该病例发生在一名26岁女性身上,表现为右侧额颞叶的囊性等密度病变。手术中可见一个柔软的黄色肿瘤,伴有囊腔。此次手术后五个月,患者接受了再次手术,发现肿瘤质地脆,易于与正常实质区分,伴有囊性成分。组织病理学检查显示多形性黄色星形细胞瘤伴恶性转化。组织学上,首次手术时的肿瘤由具有多核和泡沫细胞的多形性星形胶质细胞组成。本文呈现、讨论并举例说明了多形性黄色星形细胞瘤罕见的恶性转化病例。