Akiyama Yukinori, Suzuki Hime, Mikuni Nobuhiro
Department of Neurosurgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Pediatr Neurosurg. 2016;51(3):149-53. doi: 10.1159/000439028. Epub 2016 Jan 27.
Cases of intracranial germinoma with granulomatous reaction are rare, so a pathological diagnosis of this disease is difficult. In this report, we describe the case of a 13-year-old boy with a bilateral thalamic germinoma which initially mimicked tumefactive demyelinating disease with inflammation, based on the clinical symptoms, imaging results and histology of a biopsy specimen obtained endoscopically. Upon examination of the cerebrospinal fluid, oligoclonal bands were detected. Although his symptoms and radiological findings improved following steroid pulse treatment, they worsened dramatically almost 1 year after the first surgery and even after an additional steroid pulse treatment. Prompted by the clinical course, a second biopsy was performed, and a pathological examination of the specimen showed a two-cell pattern. The diagnosis was changed to intracranial germinoma. After chemotherapeutic treatment with etoposide and cisplatin, the patient's symptoms and radiological findings dramatically improved. We conclude that it is very challenging to distinguish germinomas with a granulomatous reaction due to other inflammatory diseases, especially when only small specimens can be obtained. Stereotactic or endoscopic biopsies should be performed using samples from several different points even if the lesions are associated with eloquent brain regions.
伴有肉芽肿反应的颅内生殖细胞瘤病例罕见,因此对该疾病进行病理诊断较为困难。在本报告中,我们描述了一名13岁男孩的病例,该男孩患有双侧丘脑生殖细胞瘤,基于临床症状、影像学结果以及通过内镜获取的活检标本的组织学检查,其最初表现类似伴有炎症的瘤样脱髓鞘疾病。在对脑脊液进行检查时,检测到了寡克隆带。尽管在接受类固醇冲击治疗后他的症状和影像学表现有所改善,但在首次手术后近1年,甚至在再次进行类固醇冲击治疗后,症状仍急剧恶化。鉴于临床病程,进行了第二次活检,标本的病理检查显示为双细胞模式。诊断改为颅内生殖细胞瘤。在用依托泊苷和顺铂进行化疗后,患者的症状和影像学表现显著改善。我们得出结论,区分因其他炎症性疾病导致的伴有肉芽肿反应的生殖细胞瘤极具挑战性,尤其是当只能获取少量标本时。即使病变与脑功能区相关,也应使用来自几个不同点的样本进行立体定向或内镜活检。