Meningioma
From Wikipedia, the free encyclopedia
| Meningioma | |
| Classification and external resources | |
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|---|---|
| A contrast enhanced CT scan of the brain, demonstrating the appearance of a Meningioma. | |
| ICD-10 | C70, D32 |
| ICD-9 | 225.2 |
| ICD-O: | M9530/0 |
| OMIM | 607174 |
| DiseasesDB | 8008 |
| eMedicine | neuro/209 radio/439 |
| MeSH | D008579 |
Meningiomas are the most common primary tumor of the central nervous system, arising from the arachnoid "cap" cells of the arachnoid villi in the meninges.[1] These tumors are usually benign in nature; however, they can be malignant.[2]
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[edit] Causes
Most cases are sporadic while some are familial. Persons who have undergone radiation to the scalp are more at risk for developing meningiomas.[3]
The most frequent genetic mutations involved in meningiomas are inactivation mutations in the neurofibromatosis 2 gene (merlin) on chromosome 22q.
Other possible genes/loci include:
[edit] Signs and symptoms
Small tumors (e.g., < 2.0 cm) are usually incidental findings at autopsy without having caused symptoms. Larger tumors can cause symptoms depending on the size and location.
- Focal seizures may be caused by meningiomas that overlie the cerebrum
- Progressive spastic weakness in legs and incontinence may be caused by tumors that overlie the parasagittal frontoparietal region.
- Sylvian tumors may cause myriad motor, sensory, aphasic, and seizure symptoms depending on the location.
- Increased intracranial pressure eventually occurs, but is less frequent than in gliomas.
[edit] Mechanism
Meningiomas arise from arachnoidal cells,[7] most of which are near the vicinity of the venous sinuses, and this is the site of greatest prevalence for meningioma formation. They are most frequently attached to the dura over the superior parasagittal surface of frontal and parietal lobes, along the sphenoid ridge, in the olfactory grooves, the sylvian region, superior cerebellum along the falx cerebri, cerebellopontine angle, and the spinal cord. The tumor is usually gray, well-circumscribed, and takes on the form of space it occupies. They are usually dome-shaped, with the base lying on the dura.
Histologically, the cells are relatively uniform, with a tendency to encircle one another, forming whorls and psammoma bodies (laminated calcific concretions).[8] They have a tendency to calcify and are highly vascularized.
[edit] Diagnosis
Meningiomas are readily visualized with contrast CT, MRI with gadolinium, and arteriography, all attributed to the fact that meningiomas are extra-axial and vascularized. CSF protein is usually elevated if lumbar puncture is attempted.
Though the majority of meningiomas are benign, they can have malignant presentations. Classification of meningiomas are based upon the WHO classification system. [9]
- Benign (Grade I) - (90%) - meningothelial, fibrous, transitional, psammomatous, angioblastic (most aggressive)
- Atypical (Grade II) - (7%) - choroid, clear cell, atypical
- Anaplastic/malignant (Grade III) - (2%) - papillary, rhabdoid, anaplastic
In a recent retrospective review of atypical and anaplastic meningioma cases, it was found that the mean overall survival for atypical meningiomas was 11.9 years vs. 3.3 years for anaplastic meningiomas. Mean relapse free survival for atypical meningiomas was 11.5 years vs. 2.7 years for anaplastic meningiomas.[10]
[edit] Treatment
[edit] Observation
Observation with close imaging follow-up can be used in select cases if a meningioma is small and asymptomatic. In a retrospective study on 43 patients, it was found that 63% of patients had no growth on follow-up, and the 37% found to have growth grew at an average of 4 mm / year.[11] In this study, younger patients were found to have tumors that were more likely to grow on repeat imaging, thus are poorer candidates for Observation.
Observation is not recommended in tumors that are already causing symptoms. Furthermore, close follow-up with imaging is required with an Observation strategy to rule out an enlarging tumor.[12]
[edit] Surgical resection
Meningiomas can usually be surgically resected with permanent cure if the tumor is superficial on the dural surface and easily accessible. Transarterial embolization has become a standard preoperative procedure in the preoperative management.[13] If invasion of the adjacent bone occurs, total removal is nearly impossible. Malignant transformation is rare.
The probability of tumor recurrence or growth after surgical resection can be estimated by the tumor's WHO Grade and by the extent of surgery by the Simpson Criteria.[14]
| Simpson Grade | Completeness of Resection | 10-year Recurrence |
|---|---|---|
| Grade I | complete removal including resection of underlying bone and associated dura | 9% |
| Grade II | complete removal + coagulation of dural attachment | 19% |
| Grade III | complete removal w/o resection of dura or coagulation | 29% |
| Grade IV | subtotal resection | 40% |
[edit] Radiation therapy
Radiation therapy may include Gamma Knife, proton beam treatment, or fractionated external beam radiation. Gamma Knife radiosurgery can be used in lieu of surgery in small tumors located away from critical structures.[15] Fractionated external beam radiation can also be used as primary treatment for tumors that are surgically unresectable, or for patients who are inoperable for medical reasons.
Radiation therapy is often considered for WHO Grade I meningiomas after subtotal (incomplete) tumor resections. The clinical decision to irradiate after a subtotal resection is somewhat controversial as no class I randomized controlled trials exists on the subject.[16] Numerous retrospective studies, however, have strongly suggested that the addition of post-operative radiation to incomplete resections improves both progression free survival (i.e. prevents tumor recurrence) and improves overall survival.[17]
In the case of a Grade II or Grade III meningioma, the current standard of care involves post-operative radiation treatment regardless of the degree of surgical resection.[18] This is due to the proportionally higher rate of local recurrence for these higher grade tumors.
[edit] Conventional chemotherapy
Current chemotherapies are likely not effective. Antiprogestin agents have been used, but with variable results.[19] Recent evidence that hydroxyurea has the capacity to shrink unresectable or recurrent meningiomas is being further evaluated.[20]
[edit] See also
[edit] References
- ^ Buetow MP, Buetow PC, Smirniotopoulos JG (November 1991). "Typical, atypical, and misleading features in meningioma". Radiographics 11 (6): 1087–106. PMID 1749851. http://radiographics.rsnajnls.org/cgi/pmidlookup?view=long&pmid=1749851. Retrieved on 2008-12-01.
- ^ Goldsmith BJ, Wara WM, Wilson CB, Larson DA (February 1994). "Postoperative irradiation for subtotally resected meningiomas. A retrospective analysis of 140 patients treated from 1967 to 1990". J. Neurosurg. 80 (2): 195–201. PMID 8283256.
- ^ Rabin BM (September 1996). "Radiation-induced changes in the central nervous system and head and neck". Radiographics 16 (5): 1055–72. PMID 8888390. http://radiographics.rsnajnls.org/cgi/reprint/16/5/1055.
- ^ Lekanne Deprez RH, Riegman PH, Groen NA, et al. (April 1995). "Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma". Oncogene 10 (8): 1521–8. PMID 7731706.
- ^ Staal FJ, van der Luijt RB, Baert MR, et al. (May 2002). "A novel germline mutation of PTEN associated with brain tumours of multiple lineages". Br. J. Cancer 86 (10): 1586–91. doi:. PMID 12085208.
- ^ Zattara-Cannoni H, Roll P, Figarella-Branger D, et al. (April 2001). "Cytogenetic study of six cases of radiation-induced meningiomas". Cancer Genet. Cytogenet. 126 (2): 81–4. PMID 11376799. http://linkinghub.elsevier.com/retrieve/pii/S0165-4608(00)00398-8.
- ^ "moon.ouhsc.edu". http://moon.ouhsc.edu/kfung/jty1/Com/Com306-1-Diss.htm. Retrieved on 2008-11-30.
- ^ "Neuropathology For Medical Students". http://www.pathology.vcu.edu/WirSelfInst/neuro_medStudents/tumor-1.html. Retrieved on 2008-11-30.
- ^ Wrobel G, Roerig P, Kokocinski F, et al. (March 2005). "Microarray-based gene expression profiling of benign, atypical and anaplastic meningiomas identifies novel genes associated with meningioma progression". Int. J. Cancer 114 (2): 249–56. doi:. PMID 15540215. http://dx.doi.org/10.1002/ijc.20733.
- ^ Yang SY et al.: Atypical and anaplastic meningiomas: prognostic implications of clinicopathological features. J Neurol Neurosurg Psychiatry. 2008 May;79(5):574-80. Epub 2007 Aug 31.
- ^ Herscovici Z, et al.: Natural history of conservatively treated meningiomas." Neurology. 2004 Sep 28;63(6):1133-4.
- ^ Olivero WC et al.: "The natural history and growth rate of asymptomatic meningiomas: a review of 60 patients." J Neurosurg. 1995 Aug;83(2):222-4
- ^ [1]
- ^ Simpson D. "The recurrence of intracranial meningiomas after surgical treatment." J Neurol Neurosurg Psychiatry. 1957 Feb;20(1):22-39.
- ^ Kullova A et al.: Gamma Knife surgery for benign meningioma. J Neurosurg. 2007 Aug;107(2):325-36.
- ^ Taylor BW et al.: The meningioma controversy: postoperative radiation therapy. Int J Radiat Oncol Biol Phys. 1988 Aug;15(2):299-304.
- ^ Goldsmith BJ et al.: Postoperative irradiation for subtotally resected meningiomas. A retrospective analysis of 140 patients treated from 1967 to 1990. J Neurosurg. 1994 Feb;80(2):195-201.
- ^ Goyal LK et al. "Local control and overall survival in atypical meningioma: a retrospective study," Int J Radiat Oncol Biol Phys. 2000 Jan 1;46(1):57-61.
- ^ Wahab M et al.: Meningioma and hormonal influences. Climacteric. 2003 Dec;6(4):285-92.
- ^ Newton HB. Hydroxyurea chemotherapy in the treatment of meningiomas. Neurosurg Focus. 2007;23(4):E11.
[edit] External links
- Meningioma information from the Mayo Clinic
- Images of meningiomas from MedPix
- CancerBackup
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