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Neema Tiwari*
Department of Clinical Hematology, King George Medical University, India
*Corresponding author: Neema Tiwari, Department of Clinical Hematology, King George Medical University, India.
Submission: December 13, 2017; Published: February 27, 2018
Right Sided Optic Meningioma in a Young Girl
Short Communication
ONSMs are rare tumors of anterior visual pathway [1]. ONSMs
arise from meningoepithelial cap cells of the arachnoids villi and
can develop at any location along the entire course of the optic
nerve sheath [2,3]. We received a case of right sided optic tumor
completely involving the eyeball requiring exentration surgery and
were sent to our department for analysis. On cut opening a firm
whicte tumor surface was seen and on microscopy a diagnosis
og meningothelial meningioma was made. The diagnosis was
confirmed by EMA positivity.
OSNMs are of two types mainly Primary and secondary
depending on their location. 40.8 years (42.5 years in women and
36.1yearsinmen;range3-80years),isthemeanageofpresentation
for the lesion. The most common presentation is unilateral with
females having highest presentation [4]. 5% of ONSMs present
bilaterally, and 65% of these bilateral lesions are intra canalicular
[5]. Bilateral and multifocal presentations of ONSMs are most
commonly found in patients with neurofibromatosis type 2 [6-8].
The pathogenesis of OSNMs is thought to be their compromise
optic nerve function mainly by mass effect on the pial vasculature
which induces ischemic changes as well as interferes with axonal
transport in the nerve [9]. Patient may present with classic triad of
visual loss, optic atrophy, and the presence of opticociliary shunt
vessels on the disc [6]. Fundus examination reveals disc edema
suggesting some manifestation of a compressive optic neuropathy
or frank optic atrophy.
Once the diagnosis of an ONSM is suspected, the diagnosis
can usually be established using MRI or high-resolution CT scan
[4]. The characteristic features of ONSMs include the presence
of calcification surrounding the nerve along with different
radiographic growth patterns: Tubular, globular, fusiform, and focal.
Definitive treatment of ONSMs is related to its vascular supply.
Surgical excision has almost always resulted in blindness in the
affected eye. This could be due to excision of the tumor along with
the affected optic nerve intra operatively or damage to the pial
vasculature [10]. Conservative management is indicated if there
is no significant progressive visual dysfunction, or intracranial
extension of the tumor.
This commentary is important in the preview of OSNMs being
a rare lesion which is seldom encountered and hence makes an
interesting case discussion.
References
1.	 Saeed P, Rootman J, Nugent RA, White VA, Mackenzie IR (2003) Optic
nerve sheath meningiomas. Ophthalmology 110(10): 2019-2030.
2.	 Turbin RE, Pokorny K (2004) Diagnosis and treatment of orbital optic
nerve sheath meningioma. Cancer Control 11(5): 334-341.
3.	 Craig WM, Gogela LJ (1949) Intraorbital meningiomas; A
clinicopathological study. Am J Ophthalmol 32(12): 1663-1680.
4.	 Dutton JJ (1993) Optic nerve sheath meningiomas. Surv Ophthalmol 37:
167-183.
5.	 Trobe JD, Glaser JS, Post JD, Page LK (1978) Bilateral optic canal
meningiomas: A case report. Neurosurgery 3(1): 68-74.
6.	 Ortiz O, Schochet SS, Kotzan JM, Kostick D (1996) Radiologic-pathologic
correlation: Meningioma of the optic nerve sheath. AJNR Am J
Neuroradiol 17(5): 901-906.
7.	 Carrasco JR, Penne RB (2004) Optic nerve sheath meningiomas and
advanced treatment options. Curr Opin Ophthalmol 15(5): 406-410.
8.	 Berman D, Miller NR (2006) New concepts in the management of optic
nerve sheath meningiomas. Ann Acad Med Singapore 35(3): 168-174.
9.	 Miller NR (2002) The evolving management of optic nerve sheath
meningiomas. Br J Ophthalmol 86(11): 1198.
10.	Turbin RE, Thompson CR, Kennerdell JS, Cockerham KP, Kupersmith MJ
(2002) A long-term outcome comparison in patients with optic nerve
sheath meningioma managed with observation, surgery, radiotherapy,
or surgery and radiotherapy. Ophthalmol 109(5): 890-900.
Short Communication
1/2Copyright © All rights are reserved by Neema Tiwari.
Volume 1 - Issue - 4
Medical & Surgical
Ophthalmology ResearchC CRIMSON PUBLISHERS
Wings to the Research
ISSN 2578-0360
Med Surg Ophthal Res Copyright © Neema Tiwari
2/2How to cite this article: Neema T. Right Sided Optic Meningioma in a Young Girl. Med Surg Ophthal Res. 1(4). MSOR.000520. 2018.
DOI: 10.31031/MSOR.2018.01.000520
Volume 1 - Issue - 4
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Right Sided Optic Meningioma in a Young Girl _Crimson Publishers

  • 1. Neema Tiwari* Department of Clinical Hematology, King George Medical University, India *Corresponding author: Neema Tiwari, Department of Clinical Hematology, King George Medical University, India. Submission: December 13, 2017; Published: February 27, 2018 Right Sided Optic Meningioma in a Young Girl Short Communication ONSMs are rare tumors of anterior visual pathway [1]. ONSMs arise from meningoepithelial cap cells of the arachnoids villi and can develop at any location along the entire course of the optic nerve sheath [2,3]. We received a case of right sided optic tumor completely involving the eyeball requiring exentration surgery and were sent to our department for analysis. On cut opening a firm whicte tumor surface was seen and on microscopy a diagnosis og meningothelial meningioma was made. The diagnosis was confirmed by EMA positivity. OSNMs are of two types mainly Primary and secondary depending on their location. 40.8 years (42.5 years in women and 36.1yearsinmen;range3-80years),isthemeanageofpresentation for the lesion. The most common presentation is unilateral with females having highest presentation [4]. 5% of ONSMs present bilaterally, and 65% of these bilateral lesions are intra canalicular [5]. Bilateral and multifocal presentations of ONSMs are most commonly found in patients with neurofibromatosis type 2 [6-8]. The pathogenesis of OSNMs is thought to be their compromise optic nerve function mainly by mass effect on the pial vasculature which induces ischemic changes as well as interferes with axonal transport in the nerve [9]. Patient may present with classic triad of visual loss, optic atrophy, and the presence of opticociliary shunt vessels on the disc [6]. Fundus examination reveals disc edema suggesting some manifestation of a compressive optic neuropathy or frank optic atrophy. Once the diagnosis of an ONSM is suspected, the diagnosis can usually be established using MRI or high-resolution CT scan [4]. The characteristic features of ONSMs include the presence of calcification surrounding the nerve along with different radiographic growth patterns: Tubular, globular, fusiform, and focal. Definitive treatment of ONSMs is related to its vascular supply. Surgical excision has almost always resulted in blindness in the affected eye. This could be due to excision of the tumor along with the affected optic nerve intra operatively or damage to the pial vasculature [10]. Conservative management is indicated if there is no significant progressive visual dysfunction, or intracranial extension of the tumor. This commentary is important in the preview of OSNMs being a rare lesion which is seldom encountered and hence makes an interesting case discussion. References 1. Saeed P, Rootman J, Nugent RA, White VA, Mackenzie IR (2003) Optic nerve sheath meningiomas. Ophthalmology 110(10): 2019-2030. 2. Turbin RE, Pokorny K (2004) Diagnosis and treatment of orbital optic nerve sheath meningioma. Cancer Control 11(5): 334-341. 3. Craig WM, Gogela LJ (1949) Intraorbital meningiomas; A clinicopathological study. Am J Ophthalmol 32(12): 1663-1680. 4. Dutton JJ (1993) Optic nerve sheath meningiomas. Surv Ophthalmol 37: 167-183. 5. Trobe JD, Glaser JS, Post JD, Page LK (1978) Bilateral optic canal meningiomas: A case report. Neurosurgery 3(1): 68-74. 6. Ortiz O, Schochet SS, Kotzan JM, Kostick D (1996) Radiologic-pathologic correlation: Meningioma of the optic nerve sheath. AJNR Am J Neuroradiol 17(5): 901-906. 7. Carrasco JR, Penne RB (2004) Optic nerve sheath meningiomas and advanced treatment options. Curr Opin Ophthalmol 15(5): 406-410. 8. Berman D, Miller NR (2006) New concepts in the management of optic nerve sheath meningiomas. Ann Acad Med Singapore 35(3): 168-174. 9. Miller NR (2002) The evolving management of optic nerve sheath meningiomas. Br J Ophthalmol 86(11): 1198. 10. Turbin RE, Thompson CR, Kennerdell JS, Cockerham KP, Kupersmith MJ (2002) A long-term outcome comparison in patients with optic nerve sheath meningioma managed with observation, surgery, radiotherapy, or surgery and radiotherapy. Ophthalmol 109(5): 890-900. Short Communication 1/2Copyright © All rights are reserved by Neema Tiwari. Volume 1 - Issue - 4 Medical & Surgical Ophthalmology ResearchC CRIMSON PUBLISHERS Wings to the Research ISSN 2578-0360
  • 2. Med Surg Ophthal Res Copyright © Neema Tiwari 2/2How to cite this article: Neema T. Right Sided Optic Meningioma in a Young Girl. Med Surg Ophthal Res. 1(4). MSOR.000520. 2018. DOI: 10.31031/MSOR.2018.01.000520 Volume 1 - Issue - 4 Your subsequent submission with Crimson Publishers will attain the below benefits • High-level peer review and editorial services • Freely accessible online immediately upon publication • Authors retain the copyright to their work • Licensing it under a Creative Commons license • Visibility through different online platforms • Global attainment for your research • Article availability in different formats (Pdf, E-pub, Full Text) • Endless customer service • Reasonable Membership services • Reprints availability upon request • One step article tracking system For possible submissions Click Here Submit Article Creative Commons Attribution 4.0 International License