Department of Pediatrics, Branch for Women and Children, Taipei City Hospital, Taipei, Taiwan, R.O.C.
J Chin Med Assoc. 2010 Aug;73(8):444-8. doi: 10.1016/S1726-4901(10)70096-4.
A primary intracranial yolk sac tumor (YST) is a type of germ cell tumor (GCT) and usually involves the pineal or suprasellar regions, as do other GCTs. Primary YST in the basal ganglia is not common, and bilateral basal ganglia involvement is even rarer. Early diagnosis is often difficult because of minimal or subtle findings without space-occupying lesions shown on neuroimaging during the early course of the disease. We report a case of primary intracranial YST encountered in the basal ganglia bilaterally and describe the clinical presentation, diagnostic problem, imaging characteristics, histopathologic features, and prognosis of the tumor. To the best of our knowledge, this is only the third reported case of primary YST confined to the basal ganglia in the literature.
原发性颅内卵黄囊瘤(YST)是一种生殖细胞瘤(GCT),通常涉及松果体或鞍上区域,其他 GCT 也是如此。基底节的原发性 YST 并不常见,双侧基底节受累更为罕见。由于疾病早期神经影像学检查未见占位性病变,表现为轻微或细微的表现,早期诊断往往较为困难。我们报告了一例双侧基底节原发性颅内 YST 的病例,并描述了肿瘤的临床表现、诊断问题、影像学特征、组织病理学特征和预后。据我们所知,这是文献中仅有的第三例局限于基底节的原发性 YST 报道。