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  2. Meningioma - Wikipedia

    en.wikipedia.org/wiki/Meningioma

    Meningioma, also known as meningeal tumor, is typically a slow-growing tumor that forms from the meninges, the membranous layers surrounding the brain and spinal cord. [1] Symptoms depend on the location and occur as a result of the tumor pressing on nearby tissue. [3] [6] Many cases never produce symptoms. [2]

  3. Optic nerve sheath meningioma - Wikipedia

    en.wikipedia.org/wiki/Optic_nerve_sheath_meningioma

    Optic nerve sheath meningiomas (ONSM) are rare benign tumors of the optic nerve. 60–70% of cases occur in middle age females, and is more common in older adults (mean age 44.7 years). It is also seen in children, but this is rare.

  4. Nervous system tumor - Wikipedia

    en.wikipedia.org/wiki/Nervous_system_tumor

    A nervous system tumor is a tumor that arises within the nervous system, either the central nervous system (CNS) or the peripheral nervous system (PNS). [1] [2] Nervous system primary tumors include various types of brain tumor and spinal tumors, such as gliomas, and meningiomas (of the CNS), and schwannomas (of the PNS) and can be either benign or malignant.

  5. Brain tumor - Wikipedia

    en.wikipedia.org/wiki/Brain_tumor

    The most common types of primary tumors in adults are meningiomas (usually benign) and astrocytomas such as glioblastomas. [1] In children, the most common type is a malignant medulloblastoma. [3] Diagnosis is usually by medical examination along with computed tomography (CT) or magnetic resonance imaging (MRI). [2]

  6. Sphenoid wing meningioma - Wikipedia

    en.wikipedia.org/wiki/Sphenoid_wing_meningioma

    The differential diagnosis for sphenoid wing meningioma includes other types of tumors such as optic nerve sheath meningioma, cranial osteosarcoma, metastases, and also sarcoidosis. Following the physical exam, the diagnosis is confirmed with neuro-imaging.

  7. Neurofibromatosis type II - Wikipedia

    en.wikipedia.org/wiki/Neurofibromatosis_type_II

    Neurofibromatosis type II (also known as MISME syndrome – multiple inherited schwannomas, meningiomas, and ependymomas) is a genetic condition that may be inherited or may arise spontaneously, and causes benign tumors of the brain, spinal cord, and peripheral nerves. The types of tumors frequently associated with NF2 include vestibular ...

  8. Nerve sheath tumor - Wikipedia

    en.wikipedia.org/wiki/Nerve_sheath_tumor

    Spinal and peripheral nerve sheath tumors may lead to a variety of symptoms depending on tumor type, location, and severity, though they do share some symptoms. [1] Some common findings for all nerve sheath tumors include: Pain [1] [6] Numbness [6] Tingling [6] Burning sensation [6] Weakness [6] Visible or palpable mass [6]

  9. Cutaneous meningioma - Wikipedia

    en.wikipedia.org/wiki/Cutaneous_meningioma

    Cutaneous meningioma, also known as heterotopic meningeal tissue, and rudimentary meningocele [1] is a developmental defect, and results from the presence of meningocytes outside the calvarium. [ 2 ] : 622

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