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optic nerve sheath meningioma
Description
Optic Nerve Sheath Meningioma (ONSM): A Rare Benign Tumor
Optic nerve sheath meningiomas (ONSMs) are rare, slow-growing benign tumors that arise from the cells surrounding the optic nerve. These tumors compress the optic nerve, leading to a range of symptoms and complications.
Key Characteristics:
- Rare occurrence: ONSMs account for approximately 1-2% of all meningiomas and 2% of all orbital tumors [5][6].
- Slow growth: The tumors grow slowly but progressively, which can lead to severe visual loss if left untreated [10].
- Critical location: The proximity of the tumor to the optic nerve makes it difficult to treat and can result in significant morbidity [5].
Symptoms and Complications:
- Vision loss: Untreated ONSMs almost always lead to progressive visual decline, color blindness, and finally complete loss of vision [5].
- Facial disfigurement: The tumor's growth can also cause facial disfigurement due to the compression of surrounding tissues [6].
Demographics:
- Age: ONSMs typically present in midlife, with a mean age at presentation ranging from 40.3 to 43.2 years [11][13].
- Gender: The tumors are more common in middle-aged females, with approximately 60-70% of cases occurring in this demographic [4].
Treatment and Management:
- Controversy: Treatment of ONSMs is still considered controversial due to the proximity of the tumor to the optic nerve [10].
- Primary radiotherapy: Primary radiotherapy is often recommended as a first-line treatment, with biopsy being contraindicated due to poorer long-term tumor control [12].
It's essential to note that each case of ONSM is unique and requires individualized management. A comprehensive evaluation by an experienced healthcare professional is necessary for accurate diagnosis and effective treatment planning.
References:
[1] Context result 1 [2] Context result 1 [3] Context result 4 [4] Context result 4 [5] Context result 5 [6] Context result 6 [7] Context result 8 [10] Context result 10 [11] Context result 11 [12] Context result 12
Additional Characteristics
- Rare, slow-growing benign tumors that arise from the cells surrounding the optic nerve.
- Compress the optic nerve, leading to vision loss and other symptoms.
- Typically present in midlife, with a higher incidence in middle-aged females.
- Treatment is controversial due to the tumor's proximity to the optic nerve.
- Primary radiotherapy is often recommended as a first-line treatment.
Signs and Symptoms
Diagnostic Tests
Treatment
Differential Diagnosis
The differential diagnosis for Optic Nerve Sheath Meningiomas (ONSM) includes several entities that can mimic the presentation and imaging findings of ONSM. Some of these conditions are:
- Optic Glioma: A type of brain tumor that arises from the optic nerve, often occurring in children [4]. It is a common differential diagnosis for ONSM, especially in pediatric patients.
- Orbital Pseudotumor: A non-specific term used to describe inflammation of the orbital tissues, which can cause enlargement of the optic nerve and mimic the appearance of an ONSM on imaging studies [3
Additional Differential Diagnoses
- Orbital Pseudotumor
- Optic Glioma
- optic nerve glioma
Additional Information
- oboInOwl#hasOBONamespace
- disease_ontology
- oboInOwl#id
- DOID:5632
- core#notation
- DOID:5632
- oboInOwl#hasDbXref
- UMLS_CUI:C0346328
- oboInOwl#hasExactSynonym
- meningioma of optic nerve sheath
- rdf-schema#label
- optic nerve sheath meningioma
- oboInOwl#inSubset
- http://purl.obolibrary.org/obo/doid#NCIthesaurus
- rdf-schema#subClassOf
- http://purl.obolibrary.org/obo/DOID_3419
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
- rdf-schema#domain
- https://w3id.org/def/predibionto#has_symptom_11708
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It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.