Arachnoid cyst overview

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Patient Information

Overview

Historical Perspective

Pathophysiology

Classification

Causes

Differentiating Arachnoid cyst from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Diagnostic Study of Choice

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: José Eduardo Riceto Loyola Junior, M.D.[2]

Overview

Arachnoid cysts are cerebrospinal fluid cysts covered by arachnoidal cells and collagen. They develop between the arachnoid membrane and the surface of the brain. Arachnoid cysts are mostly a congenital disorder.

Historical Perspective

Arachnoid cysts were first described by Richard Bright in 1831.

Pathophysiology

The exact pathophysiology of arachnoid cysts is not known.

Classification

Arachnoid cysts may be classified according to cause into 2 subtypes/groups: primary or secondary, or according to symptoms into 3 groups.

Causes

The exact cause of arachnoid cysts is not known. Researchers believe that most cases of arachnoid cysts are developmental malformations that arise from the unexplained splitting or tearing of the arachnoid membrane, being classified as primary. There are also arachnoid cysts that arise from secondary causes, such as trauma, surgery, intracranial hemorrhage and infection.

Differentiating Arachnoid Cyst from Other Diseases

The main differential diagnosis of Arachnoid cysts are epidermoid cysts. They can be differentiated using MRIs.

Epidemiology and Demographics

Arachnoid cysts occur in about 1.2% of the general population and are more frequently seen in men than in women.

Risk Factors

There is no doccumented risk factor for the development of arachnoid cysts.

Screening

There is insufficient evidence to recommend routine screening for arachnoid cysts.

Natural History, Complications and Prognosis

Prognosis of arachnoid cyst is generally excellent and is usually associated with a benign disease course, despite being symptomatic in a few patients. Most are found incidentally, and a few may, rarely, enlarge and complicate with the symptoms previously described such as hydrocephalus, seizures, hearing loss, visual changes and cervical myelopathy.

History and Symptoms

Patients with arachnoid cysts will most likely never show symptoms, even in cases where the cyst is large. Therefore, while the presence of symptoms may provoke further clinical investigation. Symptoms independent of further data cannot, and should not be, interpreted as evidence of a cyst's existence, size or location. These symptoms usually are:

Diagnostic Study of Choice

The diagnostic study of choice are MRIs as they can differentiate arachnoid cysts from all other causes of cystic CNS lesions while also presenting details about the origins, and anatomy of the cyst.

Physical Examination

Physical examination is generally not very useful as most cases of arachnoid cysts are diagnosed incidentally, but in larger cysts, depending of the affected region, there may be some findings such as:

Laboratory Findings

There are no laboratory findings associated with arachnoid cysts.

ECG Findings

There are no ECG findings associated with arachnoid cysts.

X-ray Findings

There are no x-ray findings associated with arachnoid cysts.

Echocardiographic and Ultrasonographic Findings

There are no ultrasonographic findings associated with arachnoid cysts.

CT

On brain/spine CT scan, arachnoid cysts are characterized by cystic images with similar density to CSF and non-enhancing borders, mostly found in the middle cranial fossa while they only rarely occur in the spinal cord.

MRI

On brain/spine MRI, arachnoid cysts are characterized by cystic images with similar density to CSF and non-enhancing borders, mostly found in the middle cranial fossa while they only rarely occur in the spinal cord. MRIs are more adequate than CT scans for evaluating arachnoid cysts.

Other Imaging findings

There are no other imaging findings associated with arachnoid cysts.

Other Diagnostic Studies

There are no other imaging findings associated with arachnoid cysts.

Medical Therapy

There is no medical treatment for arachnoid cysts. Some medications may be used for treating its symptoms, such as analgesics for headache, sleep aids for insomnia and other medications for the dizziness/nausea.

Surgery

There are a number of approaches in treating arachnoid cysts, the most common are:

  • Endoscopic fenestration and removal of the cyst wall (advances in neurosurgical techniques favor fenestration over shunt insertion as the preferred method for initial management).
  • Microsurgical fenestration;
  • Craniotomy followed by shunting.

Primary Prevention

There are no primary preventive measures available for arachnoid cysts.

Secondary Prevention

There are no secondary preventive measures available for arachnoid cysts.

Cost-effectivenes of Therapy

Most patients won't demand treatment. The very few who do must be assessed regarding cyst size, location and symptoms. If symptomatic, it may be a significant cause of morbidity and the costs of neurosurgical procedures, which are mostly safe and effective, may be high.

Future Investigational Therapies

Advances in neurosurgical techniques continue to improve the safeness and efficacy of the neurosurgical procedures in treating arachnoid cysts.

References