The Importance of Visual Field Testing in Idiopathic Intracranial Hypertension

2014 ◽  
Vol 20 ◽  
pp. 1067-1074
Author(s):  
Michael Wall
2019 ◽  
pp. 47-54
Author(s):  
Matthew J. Thurtell ◽  
Robert L. Tomsak

Idiopathic intracranial hypertension is a syndrome of increased intracranial pressure of unknown cause that most often occurs in obese women of childbearing age, although it can also occur in children, men, and older adults. Papilledema is usually present and can cause irreversible vision loss if left untreated. In this chapter, we begin by reviewing the symptoms of this condition, which include headache, transient visual obscurations, and pulse-synchronous tinnitus. We next review the clinical signs and common findings on formal visual field testing. We then discuss the diagnostic evaluation and review the diagnostic criteria for this condition. Lastly, we review the goals and management of this condition, which must be tailored depending on the severity of symptoms, papilledema, and vision loss.


2017 ◽  
Vol 9 (1) ◽  
pp. 74-78
Author(s):  
Anand Aggarwal ◽  
Prempal Kaur ◽  
Kanika Chhabra ◽  
Karamjit Singh ◽  
Piyush Goyal

Background: Idiopathic Intracranial Hypertension (IIH) is characterised by raised intracranial pressure (ICP) with normal cerebrospinal fluid (CSF) composition and absence of hydrocephalus or space occupying lesions. IIH is a rare disease in children. It can lead to visual impairment but prompt diagnosis and treatment in most of the cases will prevent potentially permanent visual loss. Objective: To report a rare case of Idiopathic Intracranial Hypertension in a pubertal child, clinical features, and findings of Magnetic Resonance Imaging (MRI) and visual field of this case. Case: An adolescent girl aged 14 years presented with headache and transient visual obscuration for two weeks. On examination, findings (fundus, visual field and MRI) were suggestive of Idiopathic intracranial hypertension. She did not have any classical predisposing risk factors. She recovered very well with acetazolamide and short term steroid therapy with no sequelae and clinical recurrence over a follow up of 12 months. Conclusion: This is a rare case of IIH in a child, which was confirmed on the MRI and visual field testing. 


JAMA ◽  
1963 ◽  
Vol 186 (8) ◽  
pp. 767 ◽  
Author(s):  
Richard M. Copenhaver

2019 ◽  
Vol 39 (2) ◽  
pp. 186-190 ◽  
Author(s):  
Shravani Mikkilineni ◽  
Jonathan D. Trobe ◽  
Wayne T. Cornblath ◽  
Lindsey De Lott

1993 ◽  
Vol 206 (1) ◽  
pp. 15-17 ◽  
Author(s):  
Josef Flammer ◽  
Philip Hendrickson ◽  
Andrea Lietz ◽  
Daniela Stümpfig

2010 ◽  
Vol 9 (8) ◽  
pp. 1025-1025
Author(s):  
D. A. Poggel ◽  
J. F. Rizzo ◽  
L. J. Toth ◽  
D.-S. Kim

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