Nanassis K, Tsitsopoulos P P, Marinopoulos D, Venizelos I, Tsitsopoulos P D
Deparment of Neurosurgery, Hippokration General Hospital, Aristotle University, Thessaloniki, Greece.
Cent Eur Neurosurg. 2010 Feb;71(1):50-3. doi: 10.1055/s-0029-1241180. Epub 2009 Dec 18.
Desmoplastic gangliogliomas are mixed cerebral tumors traditionally reported in infants. However, a few non-infantile cases have been documented. A case of a desmoplastic ganglioglioma in a 16-year male is presented. The patient reported severe headaches. Radiological examination revealed a large mass occupying the right frontal lobe. The lesion was totally excised. Histopathological examination confirmed the diagnosis of a desmoplastic ganglioglioma. The postoperative course was excellent. At the 10(1/2) year follow-up there was no evidence of tumor recurrence. Although desmoplastic gangliogliomas have aggressive features, complete surgical removal is the treatment of choice obviating the need for adjuvant therapy.
促纤维增生性节细胞胶质瘤是一种传统上多见于婴儿的混合性脑肿瘤。然而,也有一些非婴儿期病例的报道。本文报告了一例16岁男性的促纤维增生性节细胞胶质瘤。患者自述有严重头痛。影像学检查显示一个巨大肿块占据右额叶。该病变被完全切除。组织病理学检查确诊为促纤维增生性节细胞胶质瘤。术后恢复良好。在10年半的随访中,没有肿瘤复发的迹象。尽管促纤维增生性节细胞胶质瘤具有侵袭性特征,但完整的手术切除是首选治疗方法,无需辅助治疗。