|Spontaneous cerebrospinal fluid leak|
|Classification and external resources|
The spinal meninges
|ICD-9||339.8, 348.4, 349.0, 792.0|
Spontaneous Cerebrospinal Fluid Leak Syndrome (SCSFLS) is a medical condition in which the cerebrospinal fluid (CSF) held in and around a human brain and spinal cord leaks out of the surrounding protective sac, the dura, for no apparent reason. The dura, a tough, inflexible tissue, is the outermost of the three layers of the meninges, the system of membranes surrounding the brain and spinal cord. (The other two meningeal layers are the pia mater and the arachnoid mater).
A spontaneous cerebrospinal fluid leak is one of several types of cerebrospinal fluid leaks and occurs due to the presence of one or more holes in the dura. A spontaneous CSF leak, as opposed to other forms of CSF leaks, arises idiopathically. The loss of CSF due to the leak leads to a decreased volume inside the skull known as intracranial hypotension. SCSFLS is characterized by a severe and disabling headache, dizziness, metallic taste in the mouth, and facial weakness. A CT scan can identify the site of a cerebrospinal fluid leakage. Once identified, the leak can often be repaired by an epidural blood patch, an injection of the patient's own blood at the site of the leak.
SCSFLS afflicts 5 out of every 100,000 people. On average, the condition is developed at the age of 42, and women are twice as likely as men to develop the condition. Some people with SCSFLS chronically leak cerebrospinal fluid despite repeated attempts at patching, leading to long-term disability due to pain and nerve damage. SCSFLS was first described by German neurologist Dr. Georg Schaltenbrand in 1938 and by American physician Dr. Henry Woltman of the Mayo Clinic in the 1950s.
SCSFLS is classified into two main types, cranial leaks and spinal leaks. Cranial leaks occur in the head. In some cases, CSF can be seen dripping out of the nose or ear. Spinal leaks occur when one or more holes form in the dura along the spinal cord. Both cranial and spinal spontaneous CSF leaks cause neurological symptoms as well as Spontaneous Intracranial Hypotension, diminished volume and pressure of the cranium. For this reason, the SCSFLS is referred to as CSF hypovolemia as opposed to CSF hypotension.
|facial nerve||facial weakness
(Branch of 7)
Symptoms of cerebrospinal fluid leaks include an orthostatic headache in which the pain is worse when the patient is vertical and better when horizontal, severe dizziness and vertigo, facial numbness or weakness, double vision, a metallic taste in the mouth, nausea, and vomiting. Leaking CSF can sometimes be observed exiting through the nose or ear. Orthostatic headaches can be incapacitating  and disabling; these symptoms can be sufficiently debilitating to cause those afflicted to be unable to work.
Lack of CSF pressure and volume allows the brain to descend through the foramen magnum, or occipital bone, the large opening at the base of the skull. The lower portion of the brain is believed to stretch or impact one or more nerve complexes, thereby causing a variety of sensory symptoms. Nerve complexes that can be affected and their related symptoms are detailed in the table at right.
A spontaneous CSF leak is idiopathic; it can arise spontaneously or from an unknown cause. Various scientists and physicians have suggested that this condition may be the result of an underlying connective tissue disorder affecting the spinal dura. Some other studies have proposed that issues with the spinal venous drainage system may cause a CSF leak. According to this theory, dural holes and intracranial hypotension are symptoms caused by low pressure in the epidural space due to outflow to the heart through the inferior vena cava vein.
Cerebrospinal fluid (CSF) is produced by the brain by the choroid plexus. The brain floats in CSF and transports nutrients to the brain and spinal cord. CSF is contained by the dura mater. As holes form in the spinal dura mater, CSF leaks out into the surrounding space. The CSF is then absorbed into the spinal epidural venous plexus or soft tissues around the spine.
Diagnosis of a cerebrospinal fluid leak is performed through a combination of measurement of the CSF pressure and a scan of the spinal column for fluid leaks by use of a computed tomography myelogram (CTM). The opening fluid pressure in the spinal canal is obtained by performing a lumbar puncture, also known as a spinal tap. Once the pressure is measured, radiopaque contrast material is injected into the spinal fluid. The contrast then diffuses out through the dura sac. Once diffused, the contrast leaks through dural holes. This allows for a CTM with fluoroscopy to locate and image any sites of dura rupture via contrast seen outside the dura sac in the imagery.
Magnetic resonance imaging is historically less effective at directly imaging sites of CSF leak. MRI studies may show pachymeningeal enhancement (when the dura mater looks thick and inflammed) and an Arnold-Chiari malformation, but this may not be seen in every case. An Arnold-Chiari malformation occurs when the brain sags and has a downward displacement. This is due to the decreased volume of cerebrospinal fluid in which the brain floats. MRIs can present as completely normal, however, and are not the study of choice. In addition, in 18–46% of cases, the CSF pressure is measured as being in the normal range. An alternate method of locating the site of a CSF leak is to use heavily T2-weighted MR myelography. This has been shown to be effective in identifying the sites of a CSF leak without the need for a CT scan, lumbar puncture, and contrast. This type of MRI is effective at locating fluid collections such as CSF pooling.  MRIs done on patients sitting upright compared to those laying down demonstrated no difference in MRI results. 
When cranial CSF leak is suspected, due to discharge of fluid from the nose or ear that is potentially CSF, fluid can be collected and then tested with a beta-2 transferrin assay. This test can positively identify if the fluid is cerebrospinal fluid.
Up to 94% of those suffering from SCSFLS are initially misdiagnosed. Incorrect diagnoses include migraines, meningitis, and psychiatric disorders. The average time from onset of symptoms until definitive diagnosis is 13 months.
The treatment of choice for this condition is the surgical application of epidural blood patches, which has a 90% success rate in treating dural holes, higher than the conservative treatment of bed rest and hydration. Through the injection of a person's own blood into the area of the hole in the dura, an epidural blood patch uses blood's clotting factors to clot the sites of holes. The volume of autologous blood and number of patch attempts for patients is highly variable. If blood patches alone do not succeed in closing the dural tears, fibrin glue can be added and mixed into the autologous blood patch during a repeat treatment. This has been demonstrated to raise the level of effectiveness of forming a clot and arresting CSF leakage.
In extreme cases of intractable CSF leak, a surgical lumbar drain has been used. This procedure is believed to decrease spinal CSF volume while increasing intracranial CSF pressure and volume. This procedure restores normal intracranial CSF volume and pressure while promoting the healing of dural tears by lowering the pressure and volume in the dura. This procedure has led to positive results leading to relief of symptoms for up to one year.
Final outcomes for people with SCSFLS remain poorly studied. Some of those afflicted continue to leak CSF from one or more sites and may suffer from unremitting symptoms for many years. People with chronic SCSFLS may be disabled and unable to work.
Several complications can occur as a result of SCSFLS, including decreased cranial pressure, brain herniation, infection, blood pressure problems, transient paralysis, and development of a coma.
The primary and most serious complication of SCSFLS is Spontaneous Intracranial Hypotension, where pressure in the brain is severely decreased.  This complication leads to the hallmark symptom of severe orthostatic headaches.
People with cranial CSF leaks have a higher chance of developing meningitis than those with spinal CSF leaks. If cranial leaks last more than seven days, the chances of developing meningitis are significantly higher. Those with spinal CSF leaks do not usually develop meningitis due to the mostly aseptic conditions of the spinal dura. 
Orthostatic hypotension is another complication which occurs due to autonomic dysfunction when blood pressure drops significantly. The autonomic dysfunction is caused by compression of the brain stem, the part of the brain that controls breathing and circulation.
An Arnold-Chiari malformation is a downward displacement of lower parts of the brain through the skull opening that occurs due to a lack of CSF volume and pressure. A further, albeit rare complication of CSF leak is transient quadriplegia due to a sudden and significant loss of CSF. This loss results in hindbrain herniation and causes major compression of the upper cervical spinal cord. The quadriplegia dissipates once the patient lays supine. An extremely rare complication of SCSFLS is third nerve palsy, where the ability to move one's eyes becomes difficult and interrupted due to compression of the third cranial nerve. 
A 1994 community-based study indicated that two out of every 100,000 people suffered from SCSFLS, while a 2004 emergency room-based study indicated five per 100,000. SCSFLS generally affects the young and middle aged; the average age for onset is 42.3 years, but onset can range from ages 22 to 61. In an 11-year study, from 1992 to 2003, of patients with SCSFLS, women were found to be twice as likely to be affected as men.
Studies have shown that SCSFLS runs in families. It is suspected that genetic similarity in families includes weakness in the dura mater which leads to SCSFLS. Large scale population-based studies have not yet been conducted. While a majority of SCSFLS cases continue to be undiagnosed or misdiagnosed, an actual increase in occurrence is unlikely.
Spontaneous CSF leaks have been described by notable physicians and reported in medical journals dating back to the early 1900s. Among them were Georg Schaltenbrand, Henry Woltman of the Mayo Clinic, and a French medical journal. German neurologist Dr. Georg Schaltenbrand reported in 1938 and 1953 what he termed "aliquorrhea", a condition marked by very low, unobtainable, or even negative CSF pressures. The symptoms included orthostatic headaches and other features that are now recognized as spontaneous intracranial hypotension. A few decades earlier, the same syndrome had been described in French literature as "hypotension of spinal fluid" and "ventricular collapse". In 1940, Dr Henry Woltman wrote about "headaches associated with decreased intracranial pressure". The full clinical manifestations of intracranial hypotension and CSF leaks were described in several publications reported between the 1960s and early 1990s.
IV Cosyntropin has been used to treat CSF leaks. Cosyntropin is a corticosteroid that causes the brain to produce additional spinal fluid to replace the volume of the lost CSF and alleviate symptoms.
In a small study of two patients who suffered from recurrent CSF leaks where repeated blood patches failed to form clots and relieve symptoms, the patients received complete resolution of symptoms with an epidural saline infusion.
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|Classification and external resources|
"Spontaneous intracranial hypotension" (SIH), also known as a spontaneous low CSF (Cerebrospinal fluid) pressure headache, usually presents without any preexisting trauma or known violation of the epidural or thecal space.
The headache is usually orthostatic and related to traction on pain-sensitive intracranial and meningeal structures. The condition is benign and self limited. It may be associated with nausea, vomiting, horizontal diplopia, unsteadiness, vertigo, altered hearing, neck pain/stiffness, interscapular pain, and occasionally visual field cuts.
The diagnosis is made based on history, exclusion of competing differential diagnoses, and the following studies: MRIs with gadolinium may display diffuse patchy meningeal enhancement, "sagging" of the brain, tonsilar descent, and posterior fossa crowding. This condition is associated with low CSF opening pressure on lumbar puncture (normal CSF pressure is at least 60 mmH2O or 590 Pa).
Although conservative management should by attempted, an epidural blood patch should be attempted, as it is the treatment of choice.