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The accumulation of fluid within the air gaps of lungs and parenchyma is called Pulmonary Edema. Patients who suffer an acute deterioration of previously stable cirrhosis from alcohol or chronic hepatitis may have a life-threatening illness, but they do not have ALF. Despite its relative rarity, ALF is important because it is associated with a high mortality. Acetaminophen (one form of which is called Tylenol®) poisoning is by far the leading single cause of ALF in the US and is responsible for nearly 50% of all cases. Typically, patients who try to commit suicide via acetaminophen overdose and develop ALF have almost always taken greater than 10 grams (20 x 500 mg tablets) and often more than 20 grams in a single ingestion. Since acetaminophen is in scores of over-the-counter cold and flu products, it is not difficult to imagine how someone with severe flu symptoms might unwittingly overdose on acetaminophen.
Many patients with unintentional ALF also have chronic pain and take pills containing within a single tablet both acetaminophen and an opiate such as codeine.
Some patients with chronic pain who are prescribed Vicodin® and similar acetaminophen-opiate combinations, become tolerant to the opiate and need to take increasing amounts to control their pain. Although acetaminophen poisoning can cause profound liver injury, early institution of treatment with an antidote called N-acetyl cysteine (NAC) [Mucomyst®] can be life-saving. Scores of drugs other than acetaminophen can also produce severe liver injury (see Drug Induced hepatitis Knol).
Certain mushrooms, notably Amanita phalloides (photo), also called the "death cap", contain very potent liver toxins.
In the past, viral hepatitis B (HBV) (see Hepatitis B knol) was one of the leading causes of ALF in the US, but its incidence has been declining. Vertical transmission of the virus from mother to child at the time of birth may also occur; this is very common in China and other parts of Asia. Other viruses, including cytomegalovirus (CMV), herpes simplex virus (HSV), and adenovirus, can rarely result in ALF, especially in immunocompromised patients such as those undergoing bone marrow transplant. Characteristically, patients with ALF from Wilson disease will present with concomitant anemia from hemolysis (red cell destruction), a brownish-green pigmented ring at the junction of the white and colored parts of the eye (the so-called Kaiser-Fleisher ring), and an unusual biochemical pattern of liver injury, which are often clues to the diagnosis. Other metabolic diseases, including alpha-1 antitrypsin deficiency and tyrosinemia, can be associated with ALF in children but are extremely rare in adults.
Autoimmune hepatitis is a relatively rare condition in which the immune system of the affected individual attacks the liver in a process that is broadly analogous to liver transplant rejection, only without the transplant.
Why this occurs is not well understood, but the condition is much more common in women than in men, similar to other autoimmune conditions like rheumatoid arthritis and lupus.
ALF may rarely occur in pregnancy, usually during the last trimester and most often in patients with preeclampsia (pregnancy-associated hypertension and loss of protein in the urine). An abrupt and profound interruption of blood flow to the liver can lead to ALF, although this is rare because the liver has an unusually rich blood supply from both veins and arteries.
When all is said and done, after an extensive evaluation that includes blood testing, radiological studies, and often even liver biopsy, the cause of ALF in at least 15% of adult cases in the US remain enigmatic. One recent study from the Acute Liver Failure Study Group (see below) demonstrated that nearly 20% patients with indeterminate ALF had previously unrecognized acetaminophen poisoning when their blood was tested with a novel assay for acetaminophen-protein adducts present in the blood after acetaminophen overdose. Most patients who develop ALF become ill very rapidly, and the interval from onset of illness to near total liver collapse may be as short as a week or less. Encephalopathy, the cognitive dysfunction that is a sine qua non of ALF, may also initially be quite subtle.
Obtaining a detailed and accurate medical history from patients with ALF can be very challenging, if not impossible, due to the presence of an altered mental status.
Clues to drug-induced liver injury can sometimes be gleaned by requesting that family members or friends empty the patient's medicine cabinet into a bag and bring it to the hospital for inspection. Furthermore, the ALF patient will undergo extensive blood and urine testing both to grade the severity of the liver failure and to determine the etiology. As mentioned above, despite an extensive battery of testing, the cause of ALF in approximately 15% of adult ALF patients and almost 50% of pediatric ALF patients remains enigmatic.
Thus it is not surprising that when the liver fails suddenly, the result is a devastating illness. Thus, rapidly and accurately determining the prognosis of the ALF patient - whether his liver will spontaneously recover with medical therapy alone, or he will die without a liver transplant - is critically important. The most important antidote is N-acetylcysteine (NAC) that is used for acetaminophen poisoning. Brain swelling, also called cerebral edema, is defined as a pathological increase in total brain water leading to an increase in brain volume. The pathogenesis of cerebral edema in the setting of ALF is complex and still poorly defined, although the major brain cell type (astrocytes) and the major toxin (ammonia) involved have been identified. Diagnosing cerebral edema rapidly is essential so that therapy can be started to prevent irreversible brain damage.
However, the CT scan may be normal despite high intracranial pressures, and serial CT imaging of ALF patients is not practical.
Most of the treatments used to control cerebral edema in ALF have been borrowed from the literature on treatment of brain swelling that accompanies head trauma. Renal (kidney) failure is common in patients with ALF and may be caused by a variety of factors. A first necessary step for liver transplant is to place the patient on the United Network for Organ Sharing (UNOS) national waiting list. As a result, patients listed for transplant with ALF essentially bypass thousands of patients with chronic liver disease who are waiting on the list, often for many months or even years. Based on current UNOS policy, the "status 1" designation requires that patients with ALF be in an intensive care unit and have either kidney or respiratory failure requiring dialysis or mechanical ventilation, respectively, or an INR > 2, a lab test measuring the clotting time that when elevated signifies severe liver failure. Because the chances of rapidly dying with severe ALF are high, and the waiting times for transplant are unpredictable, listing appropriate patients with ALF as soon as they meet these criteria is important. It should be noted that, while UNOS listing is a necessary first step for liver transplant, listing is not a guarantee of liver transplant. The final decision about whether to proceed with liver transplant is often made at the time a donor organ becomes available and is one of the most difficult decisions that liver transplant physicians (hepatologists) and surgeons face. Survival following liver transplant for ALF has historically been lower than that for chronic liver disease. Since there are multiple causes of acute liver failure that all lead to essentially the same syndrome, no single measure is likely to be effective in preventing all cases. Public health initiatives, including guidelines regarding appropriate food handling, have likely also contributed by reducing the incidence of food-borne hepatitis A.
The Acute Liver Failure Study Group consists of investigators and coordinators from 23 academic medical centers, all of which perform liver transplants, that receive support from the National Institute of Diabetes, Digestive, and Kidney Diseases to study the epidemiology, outcome and pathogenesis of ALF in the US. Since the inception of the group in 1998, more than 1100 ALF patients have enrolled in the study, which includes a detailed clinical database as well as a serum and liver tissue bank.
Stravitz RT, Kramer AH, Davern T, Shaikh AO, Caldwell SH, Mehta RL, Blei AT, Fontana RJ, McGuire BM, Rossaro L, Smith AD, Lee WM; Acute Liver Failure Study Group.
Larson AM, Polson J, Fontana RJ, Davern TJ, Lalani E, Hynan LS, Reisch JS, Schiodt FV, Ostapowicz G, Shakil AO, Lee WM; Acute Liver Failure Study Group. Davern TJ 2nd, James LP, Hinson JA, Polson J, Larson AM, Fontana RJ, Lalani E, Munoz S, Shakil AO, Lee WM; Acute Liver Failure Study Group. Slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. Spinal cord abscess is swelling and irritation (inflammation) and the collection of infected material (pus) around the spinal cord. Causes A spinal cord abscess is caused by an infection inside the spine. Hydrocephalus per se is not a malformation, but a deformation due to increased pressure in the ventricles. Aqueductal stenosis (upper right)Both aqueducts are from 25 week gestation fetuses and have been photographed with the same magnification. Aqueductal atresia and aqueductal stenosis are the most common and severe causes of congenital hydrocephalus, with the Chiari II malformation (see below) being a close second. Aqueductal atresiaAqueductal atresia following intraventricular hemorrhage in a former 25 week gestation baby.
The Chiari type II malformation is a syndrome or association of anomalies characterized by a) a neural tube defect, usually a lumbosacral myelomeningocele (MMC) b) abnormalities of the posterior fossa and craniocervical junction and c) hydrocephalus. The medulla is elongated and folded dorsally because the spinal cord is held in place by the dentate ligaments and cannot move down.
The key lesion in the Chiari II malformation is probably the MMC, which is present in all Chiari II cases. The respiratory abnormality that is frequently the cause of death, and cranial nerve abnormalities in Chiari II are due to the brainstem pathology. In the Chiari type I malformation the volume of the posterior fossa is reduced leading to overcrowding and herniation of the cerebellar tonsils and dorsal cerebellum into the spinal canal. This course was produced for the use of students, residents, and staff of NEOMED and affiliated hospitals. JavaScript appears to be disabled - most features on Can Stock Photo will not function correctly.Not a member yet? Search Can Stock Photo for royalty free illustration, royalty free clipart, digital artwork, EPS vector clip art, stock illustrations, stock images, logo icon graphics, and cheap EPS format line art drawings. If the person has history of breakage in skin or wounds in any part of the skin he is prone to cellulitis infection.


Fever, skin rash, hotness in the skin, skin sore and tightened skin is some of the symptoms of cellulitis. Congestive heart, poor heart function, abnormal condition of the valves in heart or heart attacks lead to high accumulation of blood in the blood vessel of the lungs which in turn results to the fluid to be pushed out from the blood vessels to the alveoli.
The program will cover the latest developments in kidney transplantation presented by experts in the fields of transplant surgery, nephology, and pathology. Unlike such patients with acute-on-chronic liver disease, patients with ALF have the potential to completely recover normal liver function, although this is far more likely with some causes of ALF than with others. However, the dismal prognosis associated with ALF appears to be improving, at least in the West. The incidence of ALF is poorly defined but estimated to be approximately 2,000 cases per year in the United States, making it far less common than chronic liver disease. Acetaminophen is an intrinsic, dose-dependent liver toxin, which means that if any given individual takes enough acetaminophen, they will develop severe liver injury, possible culminating in ALF (see Drug-Induced Hepatitis knol). In contrast, the unintentional overdose group usually takes smaller doses but does so several times over an entire day or over several days before presenting with ALF, so that the total dose of acetaminophen ingested is usually still quite large. There are also almost certainly genetic and environmental factors that affect a given person's threshold of toxicity. Vicodin®, a combination of hydrocodone with acetaminophen, is the most common example of this type of medication, and it is currently one of the most frequently prescribed drugs in the US. Unlike acetaminophen, however, the vast majority of these drugs produce severe liver injury very rarely and not in a dose-dependent fashion.
Patients with vertically acquired hepatitis B may suffer reactivation of previously dormant and clinically silent hepatitis B, especially when exposed to immunosupression (for example, from chemotherapy), and a severe reactivation may culminate in an illness resembling ALF.
Infection with hepatitis A virus is usually transmitted by a fecal-oral route and may occur sporadically or in the setting of food or water borne outbreaks. Hepatitis E virus (HEV) is very rare in the US, but is a relatively common cause of ALF in certain parts of the world, including India.
The most common metabolic disease causing ALF in adults is Wilson Disease, a rare hereditary disorder associated with abnormal accumulation of copper in the liver and other organs. Although Wilson disease often responds to medical therapy with drugs that bind and remove copper from the body, when ALF develops the prognosis for recovery is grim, and liver transplant is usually required. Fortunately, autoimmune hepatitis usually responds to immunosuppressive therapy with steroids, but medical treatment may not be successful when the patient has advanced liver failure. Such so-called "shock liver" typically occurs in the setting of cardiac arrest, but can also be observed with severe heat stroke, massive tumor infiltration of the liver, or when the veins normally draining blood from the liver are blocked in a relatively rare condition called Budd Chiari Syndrome. This group, called indeterminate ALF, is probably comprised of multiple different causes, including esoteric viral infections, unrecognized toxic exposures, autoimmune and metabolic diseases. This suggests that acetaminophen poisoning is an even bigger problem than previously realized.
Often the illness will begin with nonspecific symptoms, including malaise, fatigue, nausea, and abdominal discomfort.
Minor changes in personality, particularly irritability, inattention, mild memory lapses, and insomnia may be the first signs.
Although certain features do help determine the prognosis in ALF, such as the cause of the ALF, the severity of the hepatic encephalopathy, and certain lab tests, none is completely accurate, making the decision about whether or not to proceed with liver transplant often quite difficult.
Patients with ALF often require admission to an intensive care unit and are probably best managed in a tertiary referral center that performs liver transplantation, which can be life saving in appropriate candidates.
The goal is to anticipate, prevent, and treat complications, and facilitate the patient's liver regeneration and repair. NAC is highly effective when given within 8-12 hours after acetaminophen overdose, but it loses some of its efficacy thereafter. Patients with rapid onset ALF (for example, from acetaminophen poisoning) seem to be at particularly high risk for suffering this complication. Unfortunately, cerebral edema may be difficult to diagnose on physical exam, although some patients will develop hypertension, a slow heart rate, abnormal reflexes, and loss of the normal reaction of the pupils to light. Thus, many experts recommend placement of an intracranial monitor, a small device placed through the skull to measure pressure within the brain directly. Studies have demonstrated that specialized, continuous forms of dialysis are superior to conventional hemodialysis in ALF patients. Thus, in most cases, patients with ALF should be managed at a medical center that offers liver transplantation as a therapeutic option.
In recognition of their very poor short-term prognosis, patients with ALF enjoy a special designation on the waiting list called "status 1" that equates to the highest priority for transplant possible. In many parts of the country, the waiting time for liver transplant for patients with status 1 listing is only 48 to 72 hours, compared with many months for those listed with chronic liver disease.
Otherwise, they may develop complications that preclude liver transplantation, such as severe and untreatable cerebral edema or multi-organ failure. Deciding to proceed with liver transplant, while potentially life saving, commits the patient not only to a major surgical procedure but also a lifetime of taking immunosuppressant and other medications. However, currently one-year survivals of greater than 80% are achieved at many programs, with some larger transplant centers reporting survivals of over 90% for transplanted ALF patients. However, several measures can be envisioned that, if successfully executed, should significantly decrease the incidence of ALF in the US. Certainly, other areas deserve attention as well, including public education about the potential dangers of eating wild mushrooms.
The ALF patient's outcome depends on the balance between liver injury on the one end and liver regeneration and repair on the other.
The group also has conducted a controlled, randomized, double blind trial of the use of an anti-oxidant, N-acetyl cysteine (NAC), for the treatment of ALF not due to acetaminophen. Acetaminophen-induced acute liver failure: results of a United States multicenter, prospective study.
Aminotransferase elevations in healthy adults receiving 4 grams of acetaminophen daily: a randomized controlled trial. Repeat exposure to incremental doses of acetaminophen provides protection against acetaminophen-induced lethality in mice: an explanation for high acetaminophen dosage in humans without hepatic injury.
Many cases of hydrocephalus are caused by acquired lesions (tumors, subarachnoid hemorrhage, meningitis) some of which are included in the above list. A few rudimentary ependymal-lined tubules outline the former aqueduct (aqueductal forking).
It may be caused by clots from intraventricular bleeding, infection, and other pathologies that cause gliosis and obliterate the aqueduct.
The abnormality of the posterior fossa and its contents consists of a large foramen magnum, low insertion of the tentorium and a shallow posterior fossa. Leakage of CSF through the MMC creates low pressure in the spinal subarachnoid space that sucks the posterior fossa contents into the spinal canal. The neuromotor deficit from the MMC is caused by the malformation of the spinal cord and is aggravated by subsequent damage of exposed neural tissue. The vermis is absent and the floor of the fourth ventricle (and floor of the posterior fossa cyst) is in plain view. Can Stock Photo has the royalty free illustration, line art drawing, EPS vector graphic, or stock clipart icon that you need. The bacteria belonging to the group of staphylococcus would cause cellulitis infection and it usually attacks the person when there is development of crack or cut in the skin. For some persons, there may be chills, fatigue, confusion, illness and muscle pain may be accompanied in the symptoms. In rare case, hospitalization is required if the infection does not subside and you have weakened immunity.
Other causes that are responsible are lung infection, cocaine smoking, radiation and lung injury.
Approximately 6% of liver transplants in the US each year are performed on patients with ALF. For example, alcohol abuse and prolonged fasting may be associated with enhanced susceptibility to acetaminophen toxicity. Patients who are addicted to the opiate component, commonly crave more and more, and thereby unwittingly consume increasing amounts of acetaminophen, ultimately leading to ALF. Unfortunately, amateur mushroom pickers all too commonly mistake Amanita phalloides for an edible variety. An infamous outbreak of hepatitis A in the Pittsburgh area in 2003 resulted in more than 650 cases of hepatitis and 4 deaths from ALF. Wilson disease typically effects children, adolescents, and young adults, but has been occasionally reported in older individuals as well. Fortunately, most patients with pregnancy-related ALF recover following expeditious delivery of the infant. Jaundice (yellowing of the skin) and scleral icterus (yellowing of the eyes) are often present, but may not be initially noted by patients or their families until relatively late in the course of the illness. However, the severity of encephalopathy may dramatically and suddenly worsen, culminating in full-blown hepatic coma in a relatively short time. Finally, an abdominal ultrasound is performed to assess the size, configuration, and texture of the liver, to verify that its vascular supply is intact, and to rule out masses or other problems. Although the survival is now much better, many patients with severe ALF still will not survive without transplant.


In such centers, ALF patients benefit from care from a large and well-orchestrated team of transplant physicians and surgeons, ICU physicians and nurses, nephrologists (kidney doctors), neurologists, and possibly neurosurgeons. The most common complications, including cerebral edema, renal failure, and infection, are discussed below. Because the brain is confined to the skull, which is relatively rigid, an increase in volume rapidly translates into an increase in pressure, which in turn can cause brain damage from loss of blood flow or even life-threatening herniation, when the brain is pushed past or through a fixed structure in the skull. In addition, certain findings on head CT scan, including loss of the normal junction between gray and white matter in the brain, compression of the normal fluid-filled spaces, and loss of the normal folds (sulci), are suggestive. This monitor, known colloquially as a "bolt", allows accurate and rapid assessment of intracranial pressure, which in turn can facilitate rapid and appropriate interventions to treat elevated pressures and prevent brain damage. Unfortunately, even with aggressive and appropriate therapy, cerebral edema may be unrelenting and result in profound brain injury or even brain death. If the ALF patient is not already hospitalized at a transplant program, it is important to consider early transfer to a liver transplant center, preferably one with experience managing patients with ALF. Obviously, patients must also meet other criteria for liver transplant candidacy (see Liver Transplant Knol). However, deciding not to proceed based on the hope that the patient's own liver will regenerate and recover, may result in a poor outcome if the patient unexpectedly takes a turn for the worse and another donor liver is not readily available.
For example, vaccination for hepatitis A and B has probably contributed to the declining incidence of ALF from viral hepatitis.
Finally, in the opinion of the author, legislative action directed at uncoupling acetaminophen-opiate drugs (like Vicodin®) would dramatically decrease the incidence of unintentional acetaminophen overdose (see Drug-induced Hepatitis knol), and this should therefore be a priority for the Food and Drug Administration and other regulatory agencies.
If the liver injury can be attenuated, or the liver repair and regenerative responses can be enhanced, then recovery is likely.
Results of a prospective study of acute liver failure at 17 tertiary care centers in the United States. Reproduced with the permission of the Department of Radiology of Akron Children's Hospital.
The aqueduct in the right upper corner is from the fetus with aqueductal stenosis illustrated in the images on the right. It is a component of complex malformations and may be inherited in autosomal recessive or X-linked patterns. Sometimes, a few rudimentary ependymal-lined tubules are seen in place of the aqueduct (aqueductal forking). As a result of these deformities, the cerebellum and brainstem are crowded and displaced into the cervical canal. The medulla, portion of the cerebellum, and the 4th ventricle lie below the foramen magnum.
One consequence of this is collapse of the aqueduct and the 4th ventricle and blockage of the foramina of Lushka, resulting in hydrocephalus.
Our designers and illustrators provide royalty free stock images, clip art, clipart graphics, and pictures for as little as 1 dollar. Usage of corticosteroid drugs for long time would suppress the immunity of the person leading to infection.
In many cases kidney failure, brain surgery or bleeding in the brain may increase the fluid level in the blood vessels.
There are significant geographical differences in the relative frequency of different causes of ALF across the world.
Eating Amanita phalloides results in a classic syndrome of severe nausea, vomiting, profuse diarrhea, and crampy abdominal pain that typically begins about 8-16 hours after eating the mushrooms. It may even be of some value in the treatment of non-acetaminophen ALF, although its role in this setting is still under investigation. In fact, most patients are in deep hepatic coma, although some display severe agitation, before this complication becomes evident. However, there are significant risks associated with bolt placement, including bleeding into the brain with dire consequences.
Doing so allows the patient to be evaluated by the transplant center staff to determine candidacy for liver transplant before the patient becomes too ill. Recent advances in molecular and cell biology have resulted in the identification of molecular targets that might soon be purposefully manipulated to tip the balance and achieve this goal.
An even larger proportion of hydrocephalus cases are caused by developmental lesions or malformations many of which have a defined genetic basis. The best known form of aqueductal stenosis is X-linked aqueductal stenosis (also known as Hydrocephalus due to Congenital Stenosis of Aqueduct of Sylvius-HSAS), caused by mutations of the L1CAM gene on Xq28. The foramina of Luschka lie in the spinal canal, and the subarachnoid space around them is collapsed and fibrotic. For this reason, cesarean section before the onset of labor and before rupture of the membranes is the preferred method of delivery of Chiari II babies. Sometimes he may ask you to do blood culture test and culture of pussy liquid from the affected part.
In adult patients in the US, most cases of ALF are related to acetaminophen poisoning, with severe liver injury from other drugs, viral hepatitis, shock liver, and other, often undefined etiologies making up the remaining cases (see table below). Within a day or two, severe liver damage can ensue, which can be life threatening even with medical therapy. The outbreak ultimately was traced to tainted green onions used and salsa served at a local Mexican restaurant. Hepatitis C (see HCV knol) is a very common cause of cirrhosis in the US but rarely if ever causes ALF. Thus, the decision to place a bolt must be individualized and rely on a carefully considered assessment of the risks and benefits for a given patient. The infection may cause inflammation and swelling, which also presses on (compresses) the spinal cord. The infection is usually due to bacteria. Some of these malformations have clear cut mechanical effects that explain the mechanism of hydrocephalus (see below). This gene encodes the L1 cell adhesion molecule which plays an important role in neuronal migration and axon guidance. Aqueductal atresia is usually associated with other disruptive brain Aqueductal atresia cannot be distinguished by MRI from aqueductal stenosis, and the MRI diagnosis of aqueductal stenosis includes both entities.
Chemical (and mechanical) damage may also occur from exposure of neural tissue to amniotic fluid and the squamous cells and lanugo hairs that float in it.
Eating wild mushrooms is thus best avoided by all but the most experienced mushroom pickers. During outbreaks of hepatitis A, it is important for close contacts of ill individuals to be treated with intravenous immunoglobulin and hepatitis A vaccine.
Some developmental forms of hydrocephalus are associated with other CNS and somatic malformations and defined syndromes. Patients with this syndrome may also have mental retardation, spasticity of the legs, adducted thumbs, absence of the corticospinal tracts, and agenesis of the corpus callosum. Severe hydrocephalus causes parts of the cortex that had been hidden in the cerebral sulci to become externalized. In that sense, the posterior fossa abnormality and hydrocephalus in Chiari II represent a deformation sequence secondary to the MMC.
This is prone to occur in open MMCs in which an amniotic-CSF fistula conveys amniotic products into the subarachnoid space, central canal, and, if the aqueduct is not blocked, even the cerebral ventricles. It may be caused by tuberculosis in some areas of the world, but it is not as common today as it was in the past. Hydrocephalus and mental retardation in some cases of aqueductal stenosis are indolent and are discovered in adult life. The surface of the brain appears to have more gyri than normal and gives the false impression of polymicrogyria.
However, in Chiari II there are other cerebral and extracerebral malformations (notably agenesis of the corpus callosum in one third of cases). Amniotic squames and lanugo hairs congeal around the brainstem, penetrate superficially into neural tissue and cause significant mechanical and chemical irritation that adds to the already existing pathology.
The most common developmental forms of hydrocephalus are those that are associated with the Chiari II malformation and aqueductal obstruction.
Early closure of the MMC by fetal surgery may prevent some of the posterior fossa changes and further protect neural tissue. Developmental hydrocephalus includes also cases due to crowding of the posterior fossa (Chiari I, skeletal dysplasias), and other poorly cases of hydrocephalus without an apparent obstruction. These features suggest a more complex etiology and pathogenesis, combining malformation and mechanical deformation. Sometimes it is not possible to completely drain the abscess. Medicines are prescribed to get rid of the infection. Some people recover completely. An untreated spinal cord abscess can lead to spinal cord compression.




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