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Posterior fossa meningiomas are uncommon lesions that can be found virtually anywhere in the infratentorial space. The management of these lesions will depend on their size, location, growth rate and clinical presentation.
These tumors can be classified according to their location as suboccipital, petrosal or tentorial cerebellar surfaces, cerebellopontine angle (CPA), fourth ventricle or petroclival meningiomas ( Table 12.1 ). Each location is related to different signs and symptoms, treatment options and surgical approaches.
Location | Incidence | Symptoms | Common surgical approaches |
---|---|---|---|
Occipital surface | 10% | Headaches, cerebellar syndrome, increased intracranial pressure, hemianopsia, visual hallucinations | Suboccipital craniotomy ± occipital craniotomy |
Lateral petrous surface | 8–10% | V, VII and VIII cranial neuropathies; brainstem and cerebellar compression syndromes | Retrosigmoid craniotomy |
CPA | 10–15% | V, VII and VIII cranial neuropathies; brainstem and cerebellar compression syndromes | Pterional craniotomy variants ± anterior petrosectomy |
Petroclival region | 10–38% | III, IV, V, VI, VII, VIII, IX, X and XI cranial neuropathies; brainstem and cerebellar compression syndromes; spasticity; headaches | Pterosal craniotomy variants ± anterior petrosectomy |
Jugular foramen | Rare | IX, X and XI cranial neuropathies; brainstem and cerebellar compression syndromes | Retrosigmoid craniotomy, transjugular variants |
Foramen magnum | 4–20% | Increased intracranial pressure; IX, X, XI and XII cranial neuropathies; brainstem and spinal cord compression syndromes | Suboccipital craniotomy ± C1 laminectomy, transoral; far lateral approach |
Pineal region | 6–8% | Increased intracranial pressure; visual symptoms; cerebellar dysfunction | Infratentorial supracerebellar craniotomy, occipital transtentorial craniotomy, supra/infratentorial trans-sinus approach |
Fourth ventricle | Rare | Headaches, increased intracranial pressure | Midline suboccipital craniotomy |
Tentorial surface | 30% | III, V, VI, VII and VIII cranial neuropathies; headaches; increased intracranial pressure; brainstem and cerebellar compression syndromes; psychomotor epilepsy | Subtemporal craniotomy, petrosal craniotomy variants, retrosigmoid craniotomy |
The patients may present with sign and symptoms secondary to compression of cranial nerves and long tracts, hydrocephalus and/or intracranial hypertension. The diagnosis is based on MRI and CT studies, which demonstrate an intense enhanced lesion after contrast administration and its relation with the surrounding posterior fossa contents.
CT angiography, magnetic resonance angio-venography (MRA/MRV) and conventional angiography are useful for preoperative vascular evaluation. The latter, although less used nowadays, is required for preoperative embolization, which can be helpful in cases where early control of the tumor's blood supply is difficult during surgery.
Different treatment options, including observation, radiosurgery and surgical resection, are available for meningiomas. Radiotherapy is useful as an adjuvant treatment for patients with atypical or malignant meningiomas and in subtotally or unresectable cases with evidence of growth. Radiosurgery is typically reserved for lesions less than 3 cm in diameter.
Surgery for posterior fossa meningiomas is considered in cases of symptomatic patients, as well as initially asymptomatic patients who have enlarging lesions and/or who develop symptoms related to their tumor.
In cases that present with ventricular obstruction, a temporary ventriculostomy or third ventriculostomy may be performed prior to the tumor resection.
Neurophysiology monitoring of long tracts and cranial nerves is typically recommended in order to minimize iatrogenic injury.
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