Ilgren E B, Stiller C A
Acta Neurochir (Wien). 1986;81(1-2):11-26. doi: 10.1007/BF01456260.
The therapeutic management of cerebellar astrocytomas is almost exclusively surgical. Although a few patients survive for long periods without treatment, the majority die without surgery. Total excision is advised to prevent recurrence which almost always follows non-total removal of tumour. Moreover, radical excision is feasible since the cerebellum has a remarkable capacity to compensate after large amounts of tissue have been removed. Morbidity is related to damage to the deep cerebellar nuclei, infiltration of the brain stem, secondary adhesions, and infection. Tumours may not be macroscopically visible at the time of first operation which in turn emphasizes the need for a detailed radiological work-up using, in particular, the CT scan. Biopsy alone, decompression alone, and/or aspiration are usually followed by rapid recurrence and no more than 30% of patients thus treated are recurrence-free five years after surgery. Approximately 40% of patients have subtotal resections and, of these, only 35% are recurrence-free five years post-operatively. Despite the high risk of recurrence following subtotal removal, subtotal excision may still be followed by prolonged survival since two thirds of the patients in the present study were still alive ten years or more after surgery. This is due in part to the unpredictable behaviour of cerebellar astrocytomas, a fact clearly demonstrated by serial CT studies of patients with partially excised tumours which demonstrate that residual tumour may occasionally regress or even remain static for many years. Total removal, when possible, is the treatment of choice and was carried out in 41% of patients in the present study. Ninety-five per cent of patients were free of recurrence for 25 years or more following total removal. In fact, recurrence following total removal has only rarely been recorded and is more often found when the initially excised tumour contains atypical and/or malignant features. Still, a benign histology does not preclude recurrence even when a total macroscopic excision has been achieved. This again emphasises the unpredictable nature of these tumours and the need for long-term radiological follow-up. Overall, operative mortality should be around 5% and even less for unilateral, hemispheric, circumscribed, nodular cerebellar astrocytomas. Conversely, the operative mortality for tumours of the vermis may approach 30% and generally increase with each subsequent operation, being maximal in the first post-operative month. Radiotherapy does not reduce the rate of recurrence nor prolong the overall survival period to death in patients with subtotal removal of tumour.(ABSTRACT TRUNCATED AT 400 WORDS)
小脑星形细胞瘤的治疗几乎完全依靠手术。虽然少数患者未经治疗也能长期存活,但大多数患者若不接受手术则会死亡。建议进行全切除以防止复发,因为肿瘤若未完全切除几乎总会复发。此外,根治性切除是可行的,因为小脑在大量组织被切除后具有显著的代偿能力。发病与小脑深部核团损伤、脑干浸润、继发性粘连及感染有关。在首次手术时,肿瘤在肉眼下可能不可见,这反过来强调了使用尤其是CT扫描进行详细影像学检查的必要性。单独活检、单独减压和/或抽吸术后通常会迅速复发,接受此类治疗的患者术后五年内无复发的比例不超过30%。约40%的患者接受了次全切除,其中只有35%在术后五年无复发。尽管次全切除后复发风险很高,但次全切除后仍可能有较长生存期,因为本研究中三分之二的患者术后十年或更长时间仍存活。这部分归因于小脑星形细胞瘤行为的不可预测性,对部分切除肿瘤患者的系列CT研究清楚地表明,残留肿瘤偶尔可能会消退甚至多年保持稳定。若有可能,全切除是首选治疗方法,本研究中41%的患者接受了全切除。全切除术后95%的患者25年或更长时间无复发。事实上,全切除后复发的情况很少被记录,更常见于最初切除的肿瘤具有非典型和/或恶性特征时。即便实现了肉眼下的全切除,良性组织学也不能排除复发。这再次强调了这些肿瘤的不可预测性以及长期影像学随访的必要性。总体而言,手术死亡率应在5%左右,对于单侧、半球形、边界清晰、结节状的小脑星形细胞瘤,死亡率甚至更低。相反,蚓部肿瘤的手术死亡率可能接近30%,且通常会随着后续每次手术而增加,在术后第一个月最高。对于肿瘤次全切除的患者,放疗并不能降低复发率,也不能延长总体生存期至死亡。(摘要截选至400字)