Cerebrospinal fluid circulates nutrients and acts as a shock absorber for the brain. It is produced by the choroid plexus and circulates through the ventricles and subarachnoid space before being reabsorbed. Disorders can involve abnormal volume and pressure like hydrocephalus. Infections and trauma can also cause pathologies involving cerebrospinal fluid.
Cerebrospinal fluid circulates nutrients and acts as a shock absorber for the brain. It is produced by the choroid plexus and circulates through the ventricles and subarachnoid space before being reabsorbed. Disorders can involve abnormal volume and pressure like hydrocephalus. Infections and trauma can also cause pathologies involving cerebrospinal fluid.
Cerebrospinal fluid circulates nutrients and acts as a shock absorber for the brain. It is produced by the choroid plexus and circulates through the ventricles and subarachnoid space before being reabsorbed. Disorders can involve abnormal volume and pressure like hydrocephalus. Infections and trauma can also cause pathologies involving cerebrospinal fluid.
Cerebrospinal fluid circulates nutrients and acts as a shock absorber for the brain. It is produced by the choroid plexus and circulates through the ventricles and subarachnoid space before being reabsorbed. Disorders can involve abnormal volume and pressure like hydrocephalus. Infections and trauma can also cause pathologies involving cerebrospinal fluid.
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Cerebrospinal Fluid
Dynamics and Pathology
Deependra Mahato, Kevin Ray, john D. Cantando, Dan E. Miulli, and Javed Siddiqi Introduction Cerebrospinal fluid (CSF) is found within the four ventricles of the brain, the subarachnoid space, and the central canal of the spinal cord. It is also called liquor cerebrospinalis. CSF circulates a variety of chemicals and nutrients necessary for normal brain function and metabolism; it also acts as a shock absorber, cushioning the brain from both day-to- day activity and traumatic events. Cerebrospinal Fluid Identification Grossly, CSF should be a colorless, odorless, serous fluid. There is an estimated 70 to 1 60 mL of fluid in the central nervous system at any given time (- 50% intracranial, 50% spinal). Certain pathological conditions will change both the chemical and the gross appearance of CSF. In the majority of cases, it is simple to ascertain whether fluid is CSF or not The following tests can determine if a fluid is CSF: • Glucose analysis: Analysis should be done immediately after collection to prevent fermentation. Nasal/lacrimal fluid or mucosal secretion will have < 5 mg/dL of glucose. A negative test is more reliable because, even with meningitis, the glucose level is usually 5 to 20 mg/dL and associated with other changes. However, there is a 45 to 75% chance of a false-positive • Beta2-transferrin: This test can be performed only by electrophoresis of at least 0.5 mL of sample. Beta2-transferrin is found only in CSF and vitreous humor. (Note: This test is not reliable in patients with liver disease or in newborns) • Ring sign: Also known as the halo, this sign is particularly useful for bloodtinged samples. A drop of suspected fluid is placed on linen; as the fluid feathers out into the surrounding area, blood and mucus will stay centrally placed, and the CSF (which is less viscous) will continue spreading, creating a clear ring around the central colored area. Chemical Regulators of Cerebrospinal Fluid Constituents of CSF are affected by secretion and absorption rates of CSF, hormones, and chemicals. The secretion rates and effects of hormones and chemicals on CSF vary from the vascular to the ventricular side of the choroid plexus Vascular side of choroid plexus Ventricular side of choroid plexus Flow Pattern of Cerebrospinal Fluid CSF from blood plasma is actively transported by the choroid plexus (80%), or invaginations of the pia mater, into the ventricles, with the remaining 10 to 20% produced by ventricular ependymal cells, brain parenchyma, and indirect cellular fluid shifts
The approximate CSF secretion is 450 mL per day, which corresponds to
a rate of 0.3 (0.35-0.37) mL/min. The CSF is in constant flow in a continuous pattern. Starting from the choroid plexus in the lateral ventricles, CSF continues through the foramen of Monro into the third ventricle and passes into the cerebral aqueduct prior to the fourth ventricle. From the fourth ventricle, fluid escapes into the cisterns and subarachnoid space via the fora men of Luschka and the foramen of Magendie. Some enters the central canal of the spinal cord, although most spinal fluid then circulates through the subar achnoid space and is reabsorbed in the venous system via the arachnoid villi. Pathology Involving Cerebrospinal Fluid Disorders of Volume and Pressure NPH Normal pressure hydrocephalus (NPH) is associated with a classic triad of symptoms: dementia, gait disturbance, and urinary incontinence. The etiology is usually idiopathic but can be secondary to other intracranial pathology, such as Alzheimer's disease, carcinomatosis, infectious meningitis, and subarach noid hemorrhage.
Diagnosis is primarily clinical, with documented
normal pressure via lumbar puncture and a full workup of other causes of dementia.
Treatment of NPH is shunting, either ventricular or,
at rare times, lumboperitoneal. Hydrocephalus Communicating and • Obstructive (noncommunicative) noncommunicating hydrocephalus hydrocephalus is blockage of the normal symptoms include nausea, vomiting, flow ofCSF, causing dilatation of the ventricles proximal to the obstruction. gait disturbance, frontal headache • Communicating (nonobstructive) (frequently worse in the morning), hydrocephalus is a disruption of the equi paresis of upward gaze, disorders of librium of secretion and absorption of sodium, and papilledema. Tem CSF, yielding an increased volume of CSF. porizing measures for relief may It is most commonly caused by include a ventricular catheter and/or malabsorption of the CSF by the diuretics (acetazolamide or arachnoid granulations. Common furosemide). etiologies include infection, hemorrhage, trauma, and noninfectious meningitis. Leptomeningeal or Arachnoid Cysts Leptomeningeal cysts are congenital fluid collections between two layers of the arachnoid.
There are two types of arachnoid cysts classified by h i s t o l o g i c a l fi n
dings: (1)simple,inwhich the lining of the cyst consistso f c e l l s capable of secreting CSF (this is the most common type of middle fossa arachnoid cyst), and (2) complex, in which the lining of the cyst is multicellular, often containing neuroglia and ependyma. Infectious and Noninfectious Irritants Causing Meningitis • Posttraumatic meningitis is usually limited to head trauma with an associated skull fracture. Organisms are most commonly gram-positive cocci and gramnegative bacilli. Trauma-Related Cerebrospinal Fluid Abnormalities • Cerebrospinal Leaks CSF leaks are associated with basal skull fractures and anterior fossa fractures resulting in otorrhea and/or rhinorrhea. Diagnosis is made by clinical exam; however, MRl, contrasted CT scans, and radionuclide cisternograms can help identify the source of the leak. Treatment consists of general measures to lower ICP, raising the head of the bed, administering acetazolamide to decrease CSF production, inserting a lumbar drain, and/or surgical repair. Surgical repair is indicated in refractory and recurrent CSF leaks. Pneumocephalus is evidence of air intracranially. Air can be intraparenchymal, intraventricular, subdural, or epidural. It is associated with a skull defect or injury to the tegmen tympani (congenital/traumatic/ related to pressure changes, e.g., deep-sea diving). • Traumatic Lumbar Puncture Traumatic lumbar puncture can occur during a procedure to obtain CSF; local trauma or disruption of nearby vascular structures can produce a traumatic tap.
Download Complete (Ebook) The easy guide to focused history taking for OSCEs by McCollum, David ISBN 9781138196520, 9781138743281, 9781315181783, 9781351723213, 9781351723220, 1138196525, 1138743283, 1315181789, 1351723219 PDF for All Chapters
Download Complete (Ebook) The easy guide to focused history taking for OSCEs by McCollum, David ISBN 9781138196520, 9781138743281, 9781315181783, 9781351723213, 9781351723220, 1138196525, 1138743283, 1315181789, 1351723219 PDF for All Chapters