Dept of Radiology, Rush Copley Medical Center, 2000 Ogden Ave, Aurora IL 60504, USA.
J Radiol Case Rep. 2020 Mar 31;14(3):1-6. doi: 10.3941/jrcr.v14i3.3814. eCollection 2020 Mar.
The following case report features a middle-aged female patient, previously diagnosed with Cowden syndrome, who presented to the hospital with symptoms of headaches and changes in vision that began with no apparent cause and persisted for almost a month. MRI of the head confirmed a diagnosis of dysplastic cerebellar gangliocytoma, also known as Lhermitte-Duclos disease. This cerebellar tumor, while extremely rare in incidence, is classified as the most common type of brain lesion in adult patients with Cowden syndrome. This report will also include a comprehensive literature review of Cowden syndrome and Lhermitte-Duclos disease, with greater emphasis on the radiologic characteristics of Lhermitte-Duclos disease.
以下病例报告介绍了一位中年女性患者,该患者先前被诊断为考登综合征,因无明显诱因出现头痛和视力改变等症状而到医院就诊,这些症状持续了将近一个月。头部 MRI 证实了发育不良性小脑神经节细胞瘤(也称为 Lhermitte-Duclos 病)的诊断。这种小脑肿瘤虽然发病率极低,但在考登综合征成年患者的脑部病变中最为常见。本报告还将对考登综合征和 Lhermitte-Duclos 病进行全面的文献复习,重点介绍 Lhermitte-Duclos 病的放射学特征。