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                                                                   Chapter 7: Tumours of the nervous system 349


                  Table 7.16 Primary intracranial tumours and their frequency
                  Type                        Tumour                                Approximate frequency (%)
                  Primary malignancy          Low-grade astrocytoma                 5–8
                                              Malignant astrocytoma                 40
                                              Oligodendroglioma                     5
                                              Ependymoma                            10% in childhood, 1% in adults
                                              Medulloblastoma                       4
                                              CNS lymphoma                          3–5
                                              Total (in all ages)                   ∼55
                  Benign                      Meningioma                            20
                                              Schwannoma (acoustic neuroma)         5–10
                                              Pituitary tumour                      10–20
                                              Other, e.g. craniopharyngioma         7
                                              Total (in all ages)                   ∼45



                  Clinical features                             and lower morbidity and mortality than standard open
                  Mass lesions within the skull produce signs and symp-  biopsy.
                  toms by three mechanisms:
                    Direct effect of the mass causing compression or infil-  Management

                    tration of the surrounding nervous tissue causes focal     Surgical debulking may be performed. Complete re-
                    neurological signs. This may also occur secondary to  section of benign tumours is preferred; however, if
                    surrounding oedema or arterial or venous compro-  close to vital structures, e.g. brainstem lesions, this is
                    mise, i.e. a stroke. Headache with focal neurology is a  not always possible.
                    typical presentation.                          Radiotherapy is used post-operatively, for unre-
                    Raised intracranial pressure (ICP) usually develops  sectable lesions or in patients unfit for surgery.

                    slowly, so does not normally cause the typical triad     Cerebral oedema is treated with corticosteroids.
                    of headache, vomiting and papilloedema. However,     Chemotherapy is used for malignant astrocytoma, to
                    brainstem, floor of the third ventricle and cerebellar  trytoprolong survival by a few months.
                    lesions tend to present initially with raised ICP:     Seizures are treated with anticonvulsants.
                    i Distortion of the upper brain stem causes impaired
                      consciousness.                            Prognosis
                    ii Compression of the medulla due to herniation  Prognosiscorrelateswithhistologictypeandgrade,post-
                      (coning) causes a third nerve lesion (due to com-  operative size, extent of the tumour and by the patient
                      pression of the ipsilateral third nerve) and sixth  characteristics (age, performance status, and duration of
                      nerve lesion (due to stretching of the contralateral  symptoms).
                      sixth nerve), ipsilateral hemiparesis, impaired con-
                      sciousness, respiratory depression, bradycardia and  Meningioma
                      death.
                    Partial or generalised tonic clonic seizures are charac-  Definition

                    teristic of many cerebral mass lesions.     Slow growing tumour arising from the meningeal cov-
                                                                ering of the brain and spinal cord.
                  Investigations
                  CT scanning will detect over 95% of intracranial tu-  Incidence
                  mours. MRI scanning, angiography is used for surgi-  They account for ∼20% of all intracranial tumours.
                  cal planning. Biopsy is required for histological diag-
                  nosis, although a radiological diagnosis may be suffi-  Age
                  cient. Stereotactic biopsy has a high diagnostic yield  Peak age 40–70 years.
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