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Idiopathic intracranial hypertension
See also in: External and Internal Eye
Other Resources UpToDate PubMed

Idiopathic intracranial hypertension

See also in: External and Internal Eye
Contributors: Lauren Patty Daskivich MD, MSHS, Brandon D. Ayres MD, Christopher Rapuano MD, Sunir J. Garg MD
Other Resources UpToDate PubMed

Synopsis

Idiopathic intracranial hypertension (IIH), historically referred to as benign intracranial hypertension or pseudotumor cerebri, is a clinical syndrome with elevated cerebrospinal fluid (CSF) pressure (> 250 mmH2O) as measured with the patient in a lateral decubitus position, with normal composition, without any evidence of hydrocephalus, mass, or structural or vascular lesions, and without any known cause. It is usually associated with headache and papilledema.

The most common presenting symptom of IIH is headache, occurring in 68%-98% of patients. The headache may be exacerbated by coughing or straining and is often severe. Other complaints may include blurred vision, loss of vision, transient obscurations of vision (may be postural), diplopia, tinnitus or intracranial noise, pain (of neck, arm, shoulder, or behind the eye), and nausea. Most patients suffer some degree of vision loss, with blindness in 10% of cases.

IIH is increasing in prevalence because of its association with obesity. It has a strong association with weight gain, particularly in young women. The estimated worldwide incidence in the general population is about 1 per 100 000 per year. Limiting subjects to women aged 20-44 in the United States who are 20% or more above their ideal body weight increases incidence to approximately 19 per 100 000. Female-to-male ratios of the disorder range from 4:1 to 15:1. Reported frequencies of obesity in individuals with IIH are 71%-94%, though obesity is less a factor in men and children younger than 10 years.

Several drugs have been associated with intracranial hypertension, most commonly tetracycline antibiotics, oral retinoids / retinols, and steroids (specifically anabolic steroids or withdrawal from long-term corticosteroid use). Estrogen hormones, nalidixic acid, nitrofurantoin, indomethacin, rofecoxib, lithium, cyclosporine, and cimetidine have also been associated with the disorder.

Medical problems such as systemic hypertension, obstructive sleep apnea, polycystic ovary syndrome, diabetes mellitus, thyroid disease, ulcerative colitis, systemic lupus erythematosus, sickle cell disease, anemia, cystinosis, and renal transplant have been associated with IIH, although some of these patients may have had undiagnosed cerebral venous sinus thrombosis. Despite awareness of various risk factors in association with IIH, the pathogenesis remains unclear.

Pediatric Patient Considerations:
IIH is found in young children as well, without the same predominance of obesity and female sex as in adults and teens. Pediatric patients are more likely to present with systemic signs and symptoms like headache, lethargy, anorexia, and drowsiness. With prompt diagnosis and treatment, these patients generally have a good prognosis.

Codes

ICD10CM:
G93.2 – Benign intracranial hypertension

SNOMEDCT:
68267002 – Benign intracranial hypertension

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References

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Last Updated:04/11/2022
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Idiopathic intracranial hypertension
See also in: External and Internal Eye
A medical illustration showing key findings of Idiopathic intracranial hypertension : Headache, Nausea/vomiting, Diplopia, Optic disc edema, Papilledema, Pulsatile tinnitus, Retroorbital pain, Vision loss, Photopsia
Ophthalmic Imaging image of Idiopathic intracranial hypertension - imageId=6552628. Click to open in gallery.
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