Department of Neurosurgery, Osaka University Graduate School of Medicine, Yamadaoka 2-2, E6 Suita, Osaka 565-0871, Japan.
J Neurooncol. 2010 May;97(3):445-50. doi: 10.1007/s11060-009-0042-y. Epub 2009 Nov 12.
We describe herein a surgically treated case of Lhermitte-Duclos disease in a 33-year-old man. The clinical presentation seemed typical in terms of symptoms, neurological signs, and neuroimaging. High and heterogenous fluorodeoxyglucose uptake in positron emission tomography study is presented and discussed. Furthermore, we performed volumetric analysis of the tumor with sequential magnetic resonance imaging over the course of 7 years before surgery, making this report the first with a long-term natural history, revealing that this rare disease entity may have a neoplastic nature.
我们在此描述了一例 33 岁男性的 Lhermitte-Duclos 病手术治疗病例。从症状、神经体征和神经影像学方面来看，临床表现似乎具有典型性。正电子发射断层扫描研究显示肿瘤呈现高摄取和异质性摄取，并对此进行了讨论。此外，我们对该肿瘤进行了长达 7 年的术前磁共振成像容积分析，这是首例具有长期自然病史的报告，表明这种罕见的疾病实体可能具有肿瘤性质。
