Brain Pathol. 2012 May;22(3):429-32. doi: 10.1111/j.1750-3639.2012.00590.x.
A 23-year-old male presented with a tonic-clonic generalized seizure. Neuroradiological examination revealed a superficial cystic mass with a mural nodule in the right fronto-parietal lobe. Histological and immunohistochemical examination were consistent with a pigmented (melanin producing) desmoplastic ganglioglioma.These tumors have been first described in childhood, one of them displaying melanin deposits. Only twenty cases of non-infantile desmoplastic gangliogliomas have been reported in the literature, none of them pigmented. According to the clinical and histomorphology (including the desmoplastic component) features, the differential diagnosis should include the ganglioglioma, the xanthoastrocytoma pleomorphic (both tumors also with pigmented forms) and the superficial desmoplastic infantile astrocytoma.
一位 23 岁男性出现强直阵挛性全面性发作。神经影像学检查显示右额顶叶有一个伴有壁结节的浅表囊性肿块。组织学和免疫组织化学检查符合色素性(产生黑色素)促结缔组织增生性神经节细胞瘤。这些肿瘤最初在儿童中描述,其中一个有黑色素沉积。文献中仅报道了 20 例非婴儿期促结缔组织增生性神经节细胞瘤,均无色素沉着。根据临床和组织形态学(包括促结缔组织增生成分)特征,鉴别诊断应包括神经节细胞瘤、黄色星形细胞瘤多形性(这两种肿瘤也有色素性形式)和浅表促结缔组织增生性婴儿型星形细胞瘤。