Ramsay D A, Bonnin J, MacDonald D R, Assis L
Department of Clinical Neurological Sciences, Victoria Hospital, London, ONT, Canada.
Clin Neuropathol. 1995 Nov-Dec;14(6):337-42.
Medulloblastomas may be difficult to recognize in late middle age and the elderly because of their rarity and their histological similarity, particularly in frozen sections, to common, poorly differentiated, metastatic tumors, notably the small cell carcinoma of lung. This report describes the occurrence of medulloblastomas in a 66-year-old male (case 1) and a 65-year-old female (case 2). Both tumors appeared radiologically as cystic cerebellar masses of irregular shape and variable intensity on magnetic resonance imaging; in each case microscopic examination revealed a primitive neuroectodermal tumor with focal astrocytic differentiation and desmoplasia. Case 1 died 23 months after surgery; an autopsy revealed extensive dissemination of the tumor to the bone marrow, small collections of malignant cells in the spinal subarachnoid space, and no evidence of local recurrence. Case 2 is well 29 months after her operation. The possibility of a medulloblastoma should be considered when a solitary cerebellar lesion is discovered in a middle-aged or elderly patient without a demonstrable extraneural primary site.
由于髓母细胞瘤罕见,且在组织学上,尤其是在冰冻切片中,与常见的低分化转移性肿瘤(特别是肺小细胞癌)相似,因此在中老年患者中可能难以识别。本报告描述了1例66岁男性(病例1)和1例65岁女性(病例2)发生髓母细胞瘤的情况。在磁共振成像上,这两个肿瘤在放射学上均表现为形状不规则、强度各异的囊性小脑肿块;在每个病例中,显微镜检查均显示为具有局灶性星形细胞分化和促纤维增生的原始神经外胚层肿瘤。病例1术后23个月死亡;尸检显示肿瘤广泛播散至骨髓,脊髓蛛网膜下腔有少量恶性细胞聚集,且无局部复发迹象。病例2术后29个月情况良好。当中老年患者发现孤立性小脑病变且无明显神经外原发部位时,应考虑髓母细胞瘤的可能性。