Deutsch M, Laurent J P, Cohen M E
Cancer. 1985 Oct 1;56(7 Suppl):1763-6. doi: 10.1002/1097-0142(19851001)56:7+<1763::aid-cncr2820561306>3.0.co;2-6.
Thirty-eight patients with newly diagnosed medulloblastoma were studied with myelography and cerebrospinal fluid (CSF) cytology studies before radiotherapy. Seventeen (45%) patients had evidence of dissemination beyond the posterior fossa. Spinal cord lesions were demonstrated in ten patients (26%). Negative results of CSF cytology studies did not preclude demonstration of cord involvement. Children younger than 5 years were more likely than older patients to have spinal cord involvement at diagnosis. Patients who were truly M-0 did better in terms of absolute survival but not relapse-free survival when compared with patients with dissemination. Myelography and cytology studies are necessary in the evaluation of all newly diagnosed patients with medulloblastoma and may also be indicated for patients with other brain tumors with a known propensity for dissemination.
对38例新诊断的髓母细胞瘤患者在放疗前进行了脊髓造影和脑脊液(CSF)细胞学检查。17例(45%)患者有后颅窝以外播散的证据。10例患者(26%)显示有脊髓病变。CSF细胞学检查结果为阴性并不能排除脊髓受累的显示。5岁以下儿童在诊断时比年龄较大的患者更易发生脊髓受累。与有播散的患者相比,真正为M-0期的患者在绝对生存方面表现较好,但无复发生存方面并非如此。脊髓造影和细胞学检查对于所有新诊断的髓母细胞瘤患者的评估是必要的,对于其他已知有播散倾向的脑肿瘤患者也可能适用。