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{{Optic nerve glioma}}
{{Optic nerve glioma}}
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==Overview==
==Overview==
==History and Symptoms==
Symptoms of optic nerve glioma include [[proptosis]], unilateral or bilateral [[visual impairment]], involuntary eyeball movement, squinting, [[vomiting]], irritability, poor feeding , [[seizures]], deficits in muscle tone and strength, daytime [[sleepiness]], decreased [[memory]] and [[brain]] function, [[weight loss]], delayed growth and [[loss of appetite]].


==History==
==History==
Patients with optic pathway gliomas most frequently present in the first decade with a median age of 6.5 years, with slowly progressive visual loss, followed later by proptosis (although this sequence may occasionally be reversed). Acute visual loss due to hemorrhage into the tumor is uncommon. Initial signs and symptoms of malignant gliomas include severe retro-orbital pain, unilateral or bilateral vision loss, and, typically, massive swelling and hemorrhage of the optic nerve head (although disc pallor may also be observed with posterior lesions).
 
==Common Symptoms==
==Common Symptoms==
Decreased vision (63%) is usually evident and can be documented with visual field examination if the child is old enough. Eventually mass effects will also occur, with proptosis and even intracranial sequelae including symptoms of raised intracranial pressure, focal neurological deficits and hydrocephalus from distortion of the midbrain. Involvement of the hypothalamus may result in polyuria or polydipsia.<ref>{{Cite web | title =Radiopedia Optic nerve glioma clinical presentation| url =http://radiopaedia.org/articles/optic-nerve-glioma }}</ref>  
Decreased vision (63%) is usually evident and can be documented with visual field examination if the child is old enough. Eventually mass effects will also occur, with [[proptosis]] and even intracranial sequelae including symptoms of raised [[intracranial pressure]], focal neurological deficits and [[hydrocephalus]] from distortion of the midbrain. Involvement of the [[hypothalamus]] may result in [[polyuria]] or [[polydipsia]].<ref name="radio"> Optic nerve glioma. Radiopedia(2015) http://radiopaedia.org/articles/optic-nerve-glioma Accessed on October 5 2015</ref>  
The symptoms are due to the tumor growing and pressing on the optic nerve and nearby structures. Symptoms may include:<ref>{{Cite web | title =Medline Plus optic nerve glioma symptoms| url =https://www.nlm.nih.gov/medlineplus/ency/article/001024.htm }}</ref>
 
*Involuntary eyeball movement
Common symptoms of optic pathway gliomas include:
*Outward bulging of one or both eyes
*[[Proptosis]]
*Unilateral or bilateral [[visual impairment]].
*Optic nerve gliomas may present with symptoms of the [[obstructive hydrocephalus]], which includes:
**[[Vomiting]]
**[[Sleepiness]]
**[[Poor feeding]]
**[[Irritability]]
**[[Seizures]]
**Deficits in muscle tone and strength
Other less common symptoms are:
*Involuntary eye ball movement
*Squinting
*Squinting
*Vision loss in one or both eyes that starts with the loss of peripheral vision and eventually leads to blindness
*[[Hypothalamic]] gliomas may present with symptoms of the [[diencephalic syndrome]], which includes:
*The child may show symptoms of diencephalic syndrome, which includes:
**Daytime [[sleepiness]]
**Daytime sleeping
**Decreased [[memory]] and [[brain]] function
**Decreased memory and brain function
**[[Delayed growth]]
**Delayed growth
**Loss of appetite and [[loss of weight]]
**Loss of appetite and body fat
*[[Precocious puberty]]- Due to involvement of hypothalamic-pituitary-gonadal axis precocious puberty may occur in 39 % of children with chiasmal optic nerve gliomas and NF-1.<ref name="pmid7869193">{{cite journal| author=Habiby R, Silverman B, Listernick R, Charrow J| title=Precocious puberty in children with neurofibromatosis type 1. | journal=J Pediatr | year= 1995 | volume= 126 | issue= 3 | pages= 364-7 | pmid=7869193 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7869193  }} </ref> In 10 to 20 percent of patients with optic pathway gliomas endocrinopathies due to hypothalamic extension are present.
 
==References==
==References==
{{reflist|2}}
{{reflist|2}}
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[[Category:Neurology]]
[[Category:Neurology]]
[[Category:Ophthalmology]]
[[Category:Ophthalmology]]
[[Category:Up-To-Date]]
[[Category:Oncology]]
[[Category:Medicine]]
[[Category:Ophthalmology]]
[[Category:Neurosurgery]]

Latest revision as of 14:47, 27 November 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Simrat Sarai, M.D. [2]

Overview

Symptoms of optic nerve glioma include proptosis, unilateral or bilateral visual impairment, involuntary eyeball movement, squinting, vomiting, irritability, poor feeding , seizures, deficits in muscle tone and strength, daytime sleepiness, decreased memory and brain function, weight loss, delayed growth and loss of appetite.

History

Common Symptoms

Decreased vision (63%) is usually evident and can be documented with visual field examination if the child is old enough. Eventually mass effects will also occur, with proptosis and even intracranial sequelae including symptoms of raised intracranial pressure, focal neurological deficits and hydrocephalus from distortion of the midbrain. Involvement of the hypothalamus may result in polyuria or polydipsia.[1]

Common symptoms of optic pathway gliomas include:

Other less common symptoms are:

  • Involuntary eye ball movement
  • Squinting
  • Hypothalamic gliomas may present with symptoms of the diencephalic syndrome, which includes:
  • Precocious puberty- Due to involvement of hypothalamic-pituitary-gonadal axis precocious puberty may occur in 39 % of children with chiasmal optic nerve gliomas and NF-1.[2] In 10 to 20 percent of patients with optic pathway gliomas endocrinopathies due to hypothalamic extension are present.

References

  1. Optic nerve glioma. Radiopedia(2015) http://radiopaedia.org/articles/optic-nerve-glioma Accessed on October 5 2015
  2. Habiby R, Silverman B, Listernick R, Charrow J (1995). "Precocious puberty in children with neurofibromatosis type 1". J Pediatr. 126 (3): 364–7. PMID 7869193.

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