Idiopathic intracranial hypertension

(Redirected from BIH)
Jump to navigation Jump to search

Pseudotumor cerebri Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating pseudotumor cerebri from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Idiopathic intracranial hypertension On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Idiopathic intracranial hypertension

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Idiopathic intracranial hypertension

CDC on Idiopathic intracranial hypertension

Idiopathic intracranial hypertension in the news

Blogs on Idiopathic intracranial hypertension

Directions to Hospitals Treating Psoriasis

Risk calculators and risk factors for Idiopathic intracranial hypertension

WikiDoc Resources for Idiopathic intracranial hypertension

Articles

Most recent articles on Idiopathic intracranial hypertension

Most cited articles on Idiopathic intracranial hypertension

Review articles on Idiopathic intracranial hypertension

Articles on Idiopathic intracranial hypertension in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Idiopathic intracranial hypertension

Images of Idiopathic intracranial hypertension

Photos of Idiopathic intracranial hypertension

Podcasts & MP3s on Idiopathic intracranial hypertension

Videos on Idiopathic intracranial hypertension

Evidence Based Medicine

Cochrane Collaboration on Idiopathic intracranial hypertension

Bandolier on Idiopathic intracranial hypertension

TRIP on Idiopathic intracranial hypertension

Clinical Trials

Ongoing Trials on Idiopathic intracranial hypertension at Clinical Trials.gov

Trial results on Idiopathic intracranial hypertension

Clinical Trials on Idiopathic intracranial hypertension at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Idiopathic intracranial hypertension

NICE Guidance on Idiopathic intracranial hypertension

NHS PRODIGY Guidance

FDA on Idiopathic intracranial hypertension

CDC on Idiopathic intracranial hypertension

Books

Books on Idiopathic intracranial hypertension

News

Idiopathic intracranial hypertension in the news

Be alerted to news on Idiopathic intracranial hypertension

News trends on Idiopathic intracranial hypertension

Commentary

Blogs on Idiopathic intracranial hypertension

Definitions

Definitions of Idiopathic intracranial hypertension

Patient Resources / Community

Patient resources on Idiopathic intracranial hypertension

Discussion groups on Idiopathic intracranial hypertension

Patient Handouts on Idiopathic intracranial hypertension

Directions to Hospitals Treating Idiopathic intracranial hypertension

Risk calculators and risk factors for Idiopathic intracranial hypertension

Healthcare Provider Resources

Symptoms of Idiopathic intracranial hypertension

Causes & Risk Factors for Idiopathic intracranial hypertension

Diagnostic studies for Idiopathic intracranial hypertension

Treatment of Idiopathic intracranial hypertension

Continuing Medical Education (CME)

CME Programs on Idiopathic intracranial hypertension

International

Idiopathic intracranial hypertension en Espanol

Idiopathic intracranial hypertension en Francais

Business

Idiopathic intracranial hypertension in the Marketplace

Patents on Idiopathic intracranial hypertension

Experimental / Informatics

List of terms related to Idiopathic intracranial hypertension

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Fahimeh Shojaei, M.D.

For patient information, click here

Template:DiseaseDisorder infobox

Overview

Idiopathic intracranial hypertension (IIH), sometimes called benign intracranial hypertension (BIH) or pseudotumor cerebri (PTC) is a neurological disorder that is characterized by increased intracranial pressure (ICP), in the absence of a tumor or other diseases affecting the brain or its lining. The main symptoms are headache and visual problems. Diagnosis requires brain scans and lumbar puncture. There are various medical and surgical treatments.

Terminology

The terms "benign" and "pseudotumor" derive from the fact that increased intracranial pressure was, especially in the era before computed tomography (CT), associated by brain tumors. Those patients in whom no tumour was found were therefore diagnosed with "pseudotumor cerebri" (a disease mimicking a brain tumor). The disease was renamed "benign intracranial hypertension" to distinguish it from intracranial hypertension due to malignancy (i.e. cancer); this was also felt to be misleading, and the name was therefore revised to "idiopathic (of no identifiable cause) intracranial hypertension".[1]

Raised ICP due to another cause (e.g. meningitis, tumor) can be classified as "secondary intracranial hypertension". The term "intracranial hypertension" is sometimes used (see IHRF) as a blanket term to describe intracranial hypertension of all aetiologies.

Historical Perspective

Classification

Pathophysiology

Pathogenesis

At least two primary mechanisms for the development of increased CSF pressure in primary IIH have been postulated: increased production of CSF and reduced resorption. Increased production may be the result of vasogenic extracellular brain edema, while decreased rebsorption may be due to low conductance of CSF outflow at the arachnoid villi.[2][3] Sørensen et al found evidence for increased water diffusion in the brain of IIH patients when compared to normal subjects.[3] It was argued that this evidence indicates abnormal convective transependymal water flow leading to brain edema. However, this theory remains controversial, as a similar study conducted by Bastin et al that used significantly disparate MR imaging protocols was unable to reproduce these findings.[4] Normal CSF flow involves production at the choroid plexuses and absorption at the cranial and spinal nerve root arachnoid villi and granulations. Impaired CSF absorption at the superior sagittal sinus or along the spinal nerve roots could therefore explain IIH and has been documented in 75-100% of IIH patients.[2] Permeability along the blood-CSF barrier varies, producing an increasing oncotic pressure gradient between the CSF and venous system in a rostral to caudal progression.[5] It is speculated that variations in this oncotic pressure contribute to or impede CSF absorption. The mechanism remains unclear however, since high CSF protein concentrations, as commonly found in Guillain-Barré syndrome or spinal tumors, can manifest as intracranial hypertension, whereas individuals with IIH frequently present with normal-to-low CSF protein findings.[2]

Causes

Differentiating Idiopathic intracranial hypertension from Other Diseases

Epidemiology and Demographics

The reported annual incidence of IIH is <20 per 100,000 persons.[6]

Risk Factors

Screening

Natural History, Complications, and Prognosis

Diagnosis

The diagnosis may be suspected on the basis of the history and examination. To confirm the diagnosis, as well as excluding alternative causes (such as a brain tumor), several investigations are required; more investigations may be performed if the history is not typical or the patient is more likely to have an alternative problem (e.g. children, the elderly).[6]

Neuroimaging, usually with computed tomography (CT/CAT) or magnetic resonance imaging (MRI), rules out mass lesions. In IIH these scans may be normal, although small or slit-like ventricles and "empty sella sign" (flattening of the pituitary gland due to increased pressure) may be seen. Some propose MRI as preferred mode of imaging in atypical cases, and suggest performance of MR venography to exclude venous obstruction or cerebral venous sinus thrombosis.[6]

Once a mass lesion has been ruled out, lumbar puncture is generally performed to measure the opening pressure, as well as to obtain cerebrospinal fluid to exclude alternative diagnoses such as low-grade viral meningitis. If the opening pressure is increased, CSF may be removed for relief (see below).[6]

Diagnostic Criteria

The original criteria for IIH were described by the American neurosurgeon Walter E. Dandy in 1937.[7] They were modified by Smith in 1985 to become the "modified Dandy criteria".[8]

Modified Dandy criteria[8]
1 Signs & symptoms of increased ICP – CSF pressure >25 cmH2O
2 No localizing signs with the exception of abducens nerve palsy
3 Normal CSF composition
4 Normal to small (slit) ventricles on imaging with no intracranial mass

A 2002 review proposed a 6-point set of criteria that required no unexplained symptoms or signs, measurement of the CSF opening pressure in the lateral decubitus (i.e. lying on the side), exclusion of any other causes on specific forms of imaging.[6]

History and Symptoms

Drug Side Effect

Signs and symptoms

Characteristic features of IIH are headache (worse in the morning, associated with nausea) and vision problems, such as double vision, transient visual obscurations, loss of peripheral sight or blurring of vision. If untreated, complete loss of vision is possible. While IIH may develop in any age group and in both males and females, it is more likely in females of fertile age (15-45) who are overweight or obese. Certain medications (hormonal contraception, vitamin A,[9] tetracycline antibiotics) may increase risk of IIH.[6]

Physical findings in IIH are is characterized by papilledema, loss of visual acuity and visual fields, and absence of focal neurological findings (e.g. face, arm or leg weakness, sensory disturbance or coordination loss). Diplopia (double vision), if present, may be due to abducens nerve palsy (the sixth cranial nerve).[6] Absence of papilledema, while making IIH less likely, is possible.[10]

Physical Examination

Laboratory Findings

Imaging Findings

Other Diagnostic Studies

Treatment

The primary goal in treatment of IIH is the prevention of visual loss and blindness. IIH is treated mainly through the attempted reduction of CSF pressure and, where applicable, weight loss. IIH may resolve after initial treatment, may go into remission and relapse at a later stage, or may continue chronically.[6]

Medical Therapy

Surgery

Surgical treatments include optic nerve sheath decompression and fenestration. In this procedure, a slit is made in the sheath of the optic nerve, which can alleviate swelling and slow or halt loss of vision.[11] Optic nerve sheath fenestration is less effective in controlling the CSF pressure (and in controlling most symptoms, such as headache), but is more effective in protecting the optic nerve from the effects of pressure.

Shunting is a neurosurgical procedure to facilitate the drainage of excess CSF (thereby reducing ICP). A shunt is essentially a silicone tube inserted somewhere in the fluid spaces of the central nervous system, which then drains CSF to the circulatory system or one of the body cavities. There are various types and configurations of shunts; lumboperitoneal (LP) shunts drain from the lumbar spine to the peritoneal cavity, while ventriculoatrial (VA) shunts run from the cerebral ventricles to the heart. Although shunts can dysfunction due to occlusion, infection, malfunction, etc., they are very effective in normalizing CSF pressures. The absence of papilledema or longstanding symptoms make successful shunting less likely.[12] Studies have shown that shunting procedures are becoming more common as the rate of severe obesity rises.[13]

In cases of severe obesity, gastric bypass surgery has been shown to lead to a marked improvement in symptoms.[14]

Prevention

Lumbar puncture

CSF pressure may be temporarily decreased by repeated "therapeutic" (as opposed to diagnostic) lumbar punctures (to remove excessive cerebrospinal fluid). However, this is generally regarded as a "holding measure" until medical or surgical treatment has been instituted.[6][13]

Medication

The best studied medical treatment is the carbonic anhydrase inhibitor acetazolamide, which reduces CSF production.[6] Other drugs such as furosemide and various diuretics, topiramate and prednisone may be used in an attempt to reduce ICP.

References

  1. Bandyopadhyay S (2001). "Pseudotumor cerebri". Arch. Neurol. 58 (10): 1699–701. PMID 11594936.
  2. 2.0 2.1 2.2 Skau M, Brennum J, Gjerris F, Jensen R (2006). "What is new about idiopathic intracranial hypertension? An updated review of mechanism and treatment". Cephalalgia. 26 (4): 384–99. doi:10.1111/j.1468-2982.2005.01055.x. PMID 16556239.
  3. 3.0 3.1 Sørensen PS, Thomsen C, Gjerris F, Schmidt J, Kjaer L, Henriksen O (1989). "Increased brain water content in pseudotumour cerebri measured by magnetic resonance imaging of brain water self diffusion". Neurol. Res. 11 (3): 160–4. PMID 2573851.
  4. Bastin ME, Sinha S, Farrall AJ, Wardlaw JM, Whittle IR (2003). "Diffuse brain oedema in idiopathic intracranial hypertension: a quantitative magnetic resonance imaging study". J. Neurol. Neurosurg. Psychiatr. 74 (12): 1693–6. PMID 14638893.
  5. Walker RW (2001). "Idiopathic intracranial hypertension: any light on the mechanism of the raised pressure?". J. Neurol. Neurosurg. Psychiatr. 71 (1): 1–5. PMID 11413251.
  6. 6.0 6.1 6.2 6.3 6.4 6.5 6.6 6.7 6.8 6.9 Friedman, DI (2002). "Diagnostic criteria for idiopathic intracranial hypertension". Neurology. 59 (10): 1492–1495. PMID 12455560. Unknown parameter |coauthors= ignored (help)
  7. Dandy WE (1937). "Intracranial pressure without brain tumor - diagnosis and treatment". Ann Surg. 106 (4): 492–513. Unknown parameter |month= ignored (help)
  8. 8.0 8.1 Smith JL (1985). "Whence pseudotumor cerebri?". Journal of clinical neuro-ophthalmology. 5 (1): 55–6. PMID 3156890.
  9. Jacobson DM, Berg R, Wall M, Digre KB, Corbett JJ, Ellefson RD (1999). "Serum vitamin A concentration is elevated in idiopathic intracranial hypertension". Neurology. 53 (5): 1114–8. PMID 10496276.
  10. Marcelis J, Silberstein SD (1991). "Idiopathic intracranial hypertension without papilledema". Arch. Neurol. 48 (4): 392–9. PMID 2012512.
  11. Banta JT, Farris BK (2000). "Pseudotumor cerebri and optic nerve sheath decompression". Ophthalmology. 107 (10): 1907–12. PMID 11013197.
  12. McGirt MJ, Woodworth G, Thomas G, Miller N, Williams M, Rigamonti D (2004). "Cerebrospinal fluid shunt placement for pseudotumor cerebri-associated intractable headache: predictors of treatment response and an analysis of long-term outcomes". J. Neurosurg. 101 (4): 627–32. PMID 15481717.
  13. 13.0 13.1 Curry WT, Butler WE, Barker FG (2005). "Rapidly rising incidence of cerebrospinal fluid shunting procedures for idiopathic intracranial hypertension in the United States, 1988-2002". Neurosurgery. 57 (1): 97–108, discussion 97–108. PMID 15987545.
  14. Sugerman HJ, Felton WL, Sismanis A, Kellum JM, DeMaria EJ, Sugerman EL (1999). "Gastric surgery for pseudotumor cerebri associated with severe obesity". Ann. Surg. 229 (5): 634–40, discussion 640–2. PMID 10235521.

Template:CNS diseases of the nervous system

de:Pseudotumor cerebri nl:Pseudotumor cerebri sv:Idiopatisk intrakraniell hypertension


Template:WikiDoc Sources