Literature DB >> 3728086

Cerebellar astrocytomas: therapeutic management.

E B Ilgren, C A Stiller.   

Abstract

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)

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Year:  1986        PMID: 3728086     DOI: 10.1007/bf01456260

Source DB:  PubMed          Journal:  Acta Neurochir (Wien)        ISSN: 0001-6268            Impact factor:   2.216


  36 in total

1.  Partially resected and irradiated cerebellar astrocytoma of childhood: malignant evolution after 28 years.

Authors:  H Budka
Journal:  Acta Neurochir (Wien)       Date:  1975       Impact factor: 2.216

2.  Astrocytoma of the brain and spinal cord; a review of 176 cases, 1940-1949.

Authors:  A R ELVIDGE; L F LEVY
Journal:  J Neurosurg       Date:  1956-09       Impact factor: 5.115

3.  Cerebellar astrocytoma in childhood.

Authors:  D D MATSON
Journal:  Pediatrics       Date:  1956-07       Impact factor: 7.124

4.  Benign (favorable) types of brain tumor; the and results (up to twenty years), with statistics of mortality and useful survival.

Authors:  G HORRAX
Journal:  N Engl J Med       Date:  1954-06-10       Impact factor: 91.245

5.  A study of 182 patients with verified astrocytoma, astroblastoma and oligodendroglioma of the brain.

Authors:  L DAVIS; J MARTIN; F PADBERG; R K ANDERSON
Journal:  J Neurosurg       Date:  1950-07       Impact factor: 5.115

6.  Cerebellar astrocytoma: malignant recurrence after prolonged postoperative survival. Case report.

Authors:  R M Scott; H T Ballantine
Journal:  J Neurosurg       Date:  1973-12       Impact factor: 5.115

7.  Primary malignant cerebellar astrocytomas in children: a signal for postoperative craniospinal irradiation.

Authors:  O M Salazar
Journal:  Int J Radiat Oncol Biol Phys       Date:  1981-12       Impact factor: 7.038

8.  Cystic cerebellar astrocytomas in childhood.

Authors:  T W Griffin; D Beaufait; J C Blasko
Journal:  Cancer       Date:  1979-07       Impact factor: 6.860

9.  Spinal cord seeding from cerebellar astrocytomas.

Authors:  K Shapiro; K Shulman
Journal:  Childs Brain       Date:  1976

10.  Cerebellar astrocytomas. Clinical characteristics and prognostic indices.

Authors:  E B Ilgren; C A Stiller
Journal:  J Neurooncol       Date:  1987       Impact factor: 4.130

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  13 in total

1.  Management of pilocytic astrocytoma.

Authors:  T Kayama; T Tominaga; T Yoshimoto
Journal:  Neurosurg Rev       Date:  1996       Impact factor: 3.042

2.  Prognosis of cerebellar astrocytomas in children.

Authors:  Francisco Villarejo; Jose Maria Belinchón de Diego; Alvaro Gómez de la Riva
Journal:  Childs Nerv Syst       Date:  2007-08-21       Impact factor: 1.475

3.  Cerebellar astrocytomas. Clinical characteristics and prognostic indices.

Authors:  E B Ilgren; C A Stiller
Journal:  J Neurooncol       Date:  1987       Impact factor: 4.130

4.  The clinical and radiological evaluation of primary brain tumors in children, Part I: Clinical evaluation.

Authors:  E D Allen; S E Byrd; C F Darling; T Tomita; M A Wilczynski
Journal:  J Natl Med Assoc       Date:  1993-06       Impact factor: 1.798

Review 5.  Cerebellar astrocytomas in children.

Authors:  J W Campbell; I F Pollack
Journal:  J Neurooncol       Date:  1996 May-Jun       Impact factor: 4.130

6.  Surgical treatment of posterior fossa tumors in infancy and childhood: techniques and results.

Authors:  D Voth; M Schwarz; M Geissler
Journal:  Neurosurg Rev       Date:  1993       Impact factor: 3.042

7.  The utility of the intracarotid Amytal procedure in determining hemispheric speech lateralization in pediatric epilepsy patients undergoing surgery.

Authors:  A C Hinz; M S Berger; G A Ojemann; C Dodrill
Journal:  Childs Nerv Syst       Date:  1994-05       Impact factor: 1.475

8.  Chemotherapy with vincristine (VCR) and etoposide (VP-16) in children with low-grade astrocytoma.

Authors:  M A Pons; J L Finlay; R W Walker; D Puccetti; R J Packer; M McElwain
Journal:  J Neurooncol       Date:  1992-10       Impact factor: 4.130

9.  Pilocytic astrocytomas of the posterior fossa. A follow-up study in 33 patients.

Authors:  C Hojer; G Hildebrandt; H Lanfermann; R Schröder; W F Haupt
Journal:  Acta Neurochir (Wien)       Date:  1994       Impact factor: 2.216

10.  Malignant cerebellar astrocytic tumours in children.

Authors:  J Shinoda; H Yamada; N Sakai; T Ando; T Hirata; H Hirayama
Journal:  Acta Neurochir (Wien)       Date:  1989       Impact factor: 2.216

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