Department of Neurosurgery, The Methodist Neurological Institute, 6560 Fannin St, Suite 944, Houston, TX 77030, USA.
J Neurooncol. 2011 Jul;103(3):733-7. doi: 10.1007/s11060-010-0410-7. Epub 2010 Sep 21.
Desmoplastic infantile ganglioglioma (DIG) is an uncommon supratentorial neuroepithelial brain tumor that typically occurs in infants younger than 24 months. Desmoplastic non-infantile ganglioglioma (DNIG) is a rare variant of this intracranial neoplasm. There are only 16 DNIG cases reported in the literature, with all patients under the age of 25 at the time of presentation. These DIG and DNIG cases were radiologically and histologically similar, with good outcome after treatment. Despite the size and high mitotic index for patients with DNIG, the prognosis is generally favorable and gross total resection is sufficient. We present a case of a 59-year-old woman with a DNIG. To the best of our knowledge, this is the first case reported of DNIG in late adulthood. Clinical presentation, histological and radiological findings are discussed.
促纤维增生型婴儿型神经节胶质瘤(DIG)是一种罕见的幕上神经上皮脑肿瘤,通常发生在 24 个月以下的婴儿中。促纤维增生型非婴儿型神经节胶质瘤(DNIG)是这种颅内肿瘤的罕见变体。文献中仅报道了 16 例 DNIG 病例,所有患者在就诊时均未满 25 岁。这些 DIG 和 DNIG 病例在影像学和组织学上相似,治疗后预后良好。尽管 DNIG 患者的肿瘤体积较大且有较高的有丝分裂指数,但总体预后良好,广泛全切除即可。我们报告了一例 59 岁女性的 DNIG 病例。据我们所知,这是首例报道的成年后期 DNIG 病例。讨论了其临床表现、组织学和影像学表现。