Arachnoid Cysts
Arachnoid
Cysts
Syringomyelia
Arachnoiditis
Central Nervous System Cysts
Subarachnoid Space
Cranial Fossa, Middle
Hematoma, Subdural
Cranial Fossa, Posterior
Subdural Effusion
Dura Mater
Spinal Cord Compression
Hernia
Magnetic Resonance Imaging
Neuroendoscopy
Cerebral Ventriculography
Decompression, Surgical
Laminectomy
Iophendylate
Spinal Cord Diseases
Headache
Cerebrospinal Fluid Shunts
Hypothalamic Diseases
Epidermal Cyst
Cisterna Magna
Petrous Bone
Sella Turcica
Hydrocephalus
Hematoma, Subdural, Chronic
Cerebellar Diseases
Tomography, X-Ray Computed
Ventriculoperitoneal Shunt
Cranial Nerve Diseases
Barotrauma
Paroxysmal kinesigenic choreoathetosis associated with frontotemporal arachnoid cyst--case report. (1/167)
A 17-year-old male presented with paroxysmal kinesigenic choreoathetosis (PKC) associated with frontotemporal arachnoid cyst. Xenon-133 single photon emission computed tomography detected a slight but equivocal decrease in regional cerebral blood flow in the vicinity of basal ganglia associated with the PKC episodes. PKC continued after surgical removal of the cyst but was well controlled by oral administration of carbamazepine. Whether the pathogenesis of symptomatic PKC was associated with the cortical lesion could not be determined in the present case. (+info)Heading injury precipitating subdural hematoma associated with arachnoid cysts--two case reports. (2/167)
A 14-year-old boy and a 11-year-old boy presented with subdural hematomas as complications of preexisting arachnoid cysts in the middle cranial fossa, manifesting as symptoms of raised intracranial pressure. Both had a history of heading the ball in a soccer game about 7 weeks and 2 days before the symptom occurred. There was no other head trauma, so these cases could be described as "heading injury." Arachnoid cysts in the middle cranial fossa are often associated with subdural hematomas. We emphasize that mild trauma such as heading of the ball in a soccer game may cause subdural hematomas in patients with arachnoid cysts. (+info)Lumbosacral extradural arachnoid cysts: diagnostic and indication for surgery. (3/167)
No critical discussion of the indication for the surgical treatment of lumbosacral extradural arachnoid cysts is found in the literature. Therefore, we want to compare the results in patients with operative and conservative treatment to define standards for a good surgical result. Over a period of 9 years, we operated on eight patients with a lumbosacral extradural arachnoid cyst and treated eight others conservatively. Only three of the operated patients experienced a postoperative relief of pain, but none was symptom free. The only one with continuing success had a preoperative history of 1 year only. MRI scans without contrast agent were misinterpreted in one included and one excluded case. The results of conservative treatment were nearly the same as those of operative treatment. MRI is the best diagnostic tool, but a variety of sequences must be used. Patients with a short pain history and a clear neurological deficit profited most from surgery. Patients with slight and not clearly related uncharacteristic symptoms should be excluded from surgery. (+info)Intracerebral cystic meningioma--case report. (4/167)
A 46-year-old female presented with persistent bifrontal headache. Computed tomography revealed a large cystic tumor in the right temporoparietal area, which included a solid component. The tumor had no attachment to the dura. There was no peritumoral edema or mass effect usually found around cystic meningiomas. The solid component was totally removed. Histological examination indicated that the tumor was a fibrous meningioma. Intracerebral meningioma with a large cystic component without dural attachment should be considered in the differential diagnosis of cystic cerebral tumors. (+info)Intracystic hemorrhage of the middle fossa arachnoid cyst and subdural hematoma caused by ruptured middle cerebral artery aneurysm. (5/167)
We report a case of a cerebral aneurysm arising from the bifurcation of the left middle cerebral artery that ruptured into a left middle cranial fossa arachnoid cyst, associated with acute subdural hematoma. We discuss the relationships of aneurysm, arachnoid cyst, and subdural hematoma. (+info)The role of endoscopic fenestration procedures for cerebral arachnoid cysts. (6/167)
Recently, endoscopic procedures have been recommended as the first surgical option for cerebral arachnoid cyst (AC). The author reports seven ACs treated endoscopically and discuss the role of endoscopic fenestration. The age of the patients ranged from two to 62 years. Three ACs were located in the posterior cranial fossa, two in the suprasellar area, one in the middle cranial fossa, and one in the convexity. All cases were examined by cine magnetic resonance (MR) flow study. The patient's symptoms included headache, vomiting, dizziness, problems in balance, visual disturbance, and seizure. The author performed a cysto-cisternostomy or cysto-ventriculostomy via a single burr hole. The follow-up periods ranged from six to 18 months. There was no mortality or morbidity except one case of intracisternal bleeding during endoscopic procedure. Symptoms were relieved in all seven patients. Follow-up imaging studies revealed a decrease in the size or disappearance of the cysts. The results support that the minimal fenestration procedure as possibly as preserving the internal environment is valuable for the management of ACs. (+info)Neurodevelopmental outcome after antenatal diagnosis of posterior fossa abnormalities. (7/167)
Posterior fossa abnormalities are sonographically diagnosable in the fetus. Anomalies of this region include Dandy-Walker malformation, enlarged cisterna magna, and arachnoid cyst. Despite prenatal diagnosis, the uncertainties related to natural history and neurodevelopmental outcome in survivors make patient counseling difficult. The purposes of this study were to determine the accuracy of prenatal diagnosis of these lesions and elucidate long-term neurodevelopmental outcome in survivors in prenatally diagnosed posterior fossa abnormalities. Fifteen cases of posterior fossa abnormalities were reviewed. Antenatal diagnoses of Dandy-Walker malformation was made in 13 of these cases, arachnoid cyst in one case, and enlarged cisterna magna in one case. Hydrocephalus was present in 66% of patients. The sonographic diagnosis was concordant with the pathologic or neonatal radiologic diagnosis in 13 of 15 cases. Seven fetuses (47%) exhibited additional cranial or extracranial anomalies. A karyotypic abnormality (trisomy 18) was found in one of 15 cases of posterior fossa abnormalities. Neurodevelopmental delay was present in 80% of survivors with follow-up study to 4 years of age. Prenatal diagnosis of posterior fossa abnormalities is highly accurate, yet the differential diagnosis can be challenging. Cognitive and psychomotor developmental delays remain commonplace despite early diagnosis and treatment. The approach with families in cases of prenatal diagnosis of posterior fossa abnormalities should include a search for additional central nervous system and extra-central nervous system anomalies in the fetus and counseling of parents regarding potential adverse outcome for survivors. (+info)Dandy-Walker syndrome successfully treated with cystoperitoneal shunting--case report. (8/167)
A neonate presented with Dandy-Walker syndrome manifesting as a large posterior cranial fossa cyst, aplasia of the lower cerebellar vermis, and elevation of the confluence of the sinuses but without hydrocephalus. A cystoperitoneal shunt was placed at one month after birth. The cyst diminished in size, and marked development of the cerebellar hemispheres and descent of the confluence of sinuses were observed, but not vermis development. The primary pathology of Dandy-Walker syndrome is posterior cranial fossa cyst formation due to passage obstruction in the fourth ventricle exit area and aplasia of the lower cerebellar vermis. The first choice of treatment in patients with Dandy-Walker syndrome in whom the cerebral aqueduct is open is cystoperitoneal shunt surgery, regardless of the presence or absence of hydrocephalus. (+info)Arachnoid cysts are fluid-filled sacs that form between the layers of protective tissue (meninges) that cover the brain and spinal cord. They are typically benign and may or may not cause symptoms. Arachnoid cysts are relatively rare, and their exact cause is unknown. However, they may be associated with other congenital anomalies or neurological conditions.
Symptoms of Arachnoid Cysts[2]
The symptoms of arachnoid cysts can vary depending on the size and location of the cyst. Some common symptoms include:
1. Headaches
2. Seizures
3. Nausea and vomiting
4. Abnormal eye movements
5. Weakness or numbness in the arms or legs
6. Confusion or disorientation
Diagnosis of Arachnoid Cysts[3]
Arachnoid cysts are typically diagnosed using a combination of imaging tests, such as:
1. CT scans
2. MRI scans
3. Ultrasound
Treatment of Arachnoid Cysts[4]
The treatment of arachnoid cysts depends on the size and location of the cyst, as well as the symptoms it is causing. In some cases, arachnoid cysts may not require treatment and can be monitored with regular imaging tests. However, if the cyst is causing symptoms or is growing in size, surgery may be necessary to remove the cyst.
Prognosis of Arachnoid Cysts[5]
The prognosis for arachnoid cysts is generally good, and most people with these cysts lead normal lives. However, in some cases, arachnoid cysts can cause serious complications, such as infection or bleeding, which can be life-threatening. It is important to seek medical attention if symptoms persist or worsen over time.
In conclusion, arachnoid cysts are fluid-filled sacs that form between the layers of protective tissue (meninges) covering the brain and spinal cord. While they are generally benign, they can cause a variety of symptoms and complications. If you suspect that you or someone you know may have an arachnoid cyst, it is important to seek medical attention for proper diagnosis and treatment.
References:
[1] "Arachnoid Cysts." American Association of Neurological Surgeons, 2022,
[2] "Arachnoid Cyst." Mayo Clinic, 2022,
[3] "Arachnoid Cysts." MedlinePlus, 2022,
[4] "Arachnoid Cyst: Types, Symptoms, Causes, Diagnosis, Treatment." Health Line, 2022,
There are many different types of cysts that can occur in the body, including:
1. Sebaceous cysts: These are small, usually painless cysts that form in the skin, particularly on the face, neck, or torso. They are filled with a thick, cheesy material and can become inflamed or infected.
2. Ovarian cysts: These are fluid-filled sacs that form on the ovaries. They are common in women of childbearing age and can cause pelvic pain, bloating, and other symptoms.
3. Kidney cysts: These are fluid-filled sacs that form in the kidneys. They are usually benign but can cause problems if they become large or infected.
4. Dermoid cysts: These are small, usually painless cysts that form in the skin or organs. They are filled with skin cells, hair follicles, and other tissue and can become inflamed or infected.
5. Pilar cysts: These are small, usually painless cysts that form on the scalp. They are filled with a thick, cheesy material and can become inflamed or infected.
6. Epidermoid cysts: These are small, usually painless cysts that form just under the skin. They are filled with a thick, cheesy material and can become inflamed or infected.
7. Mucous cysts: These are small, usually painless cysts that form on the fingers or toes. They are filled with a clear, sticky fluid and can become inflamed or infected.
8. Baker's cyst: This is a fluid-filled cyst that forms behind the knee. It can cause swelling and pain in the knee and is more common in women than men.
9. Tarlov cysts: These are small, fluid-filled cysts that form in the spine. They can cause back pain and other symptoms, such as sciatica.
10. ganglion cysts: These are noncancerous lumps that form on the joints or tendons. They are filled with a thick, clear fluid and can cause pain, swelling, and limited mobility.
It's important to note that this is not an exhaustive list and there may be other types of cysts that are not included here. If you suspect that you have a cyst, it's always best to consult with a healthcare professional for proper diagnosis and treatment.
The exact cause of syringomyelia is not fully understood, but it is believed to be related to abnormal development or blockage of the spinal cord during fetal development. Some cases may be associated with genetic mutations or other inherited conditions, while others may be caused by acquired factors such as trauma, infection, or tumors.
Symptoms of syringomyelia can vary widely and may include:
1. Pain: Pain is a common symptom of syringomyelia, particularly in the neck, back, or limbs. The pain may be aching, sharp, or burning in nature and may be exacerbated by movement or activity.
2. Muscle weakness: As the syrinx grows, it can compress and damage the surrounding nerve fibers, leading to muscle weakness and wasting. This can affect the limbs, face, or other areas of the body.
3. Paresthesias: Patients with syringomyelia may experience numbness, tingling, or burning sensations in the affected area.
4. Spasticity: Some individuals with syringomyelia may experience spasticity, which is characterized by stiffness and increased muscle tone.
5. Sensory loss: In severe cases of syringomyelia, patients may experience loss of sensation in the affected area.
6. Bladder dysfunction: Syringomyelia can also affect the bladder and bowel function, leading to urinary retention or incontinence.
7. Orthostatic hypotension: Some patients with syringomyelia may experience a drop in blood pressure when standing, leading to dizziness or fainting.
Diagnosis of syringomyelia is typically made through a combination of imaging studies such as MRI or CT scans, and clinical evaluation. Treatment options vary depending on the underlying cause and severity of the condition, but may include:
1. Physical therapy to maintain muscle strength and prevent deformities.
2. Orthotics and assistive devices to improve mobility and function.
3. Pain management with medication or injections.
4. Surgery to release compressive lesions or remove tumors.
5. Chemotherapy to treat malignant causes of syringomyelia.
6. Shunting procedures to drain cerebrospinal fluid and relieve pressure.
7. Rehabilitation therapies such as occupational and speech therapy to address any cognitive or functional deficits.
It's important to note that the prognosis for syringomyelia varies depending on the underlying cause and severity of the condition. In some cases, the condition may be manageable with treatment, while in others it may progress and lead to significant disability or death. Early diagnosis and intervention are key to improving outcomes for patients with syringomyelia.
Arachnoiditis can be caused by a variety of factors, such as infection, injury, or certain medical procedures. It is often difficult to diagnose, as the symptoms can be similar to those of other conditions, and there is no specific test for it. Treatment options are limited and may include pain medication, physical therapy, and other supportive measures.
Arachnoiditis is a rare condition, but it can have a significant impact on quality of life for those affected. It is important to seek medical attention if symptoms persist or worsen over time, as early diagnosis and treatment may improve outcomes.
Central nervous system cysts are typically diagnosed through imaging tests such as CT or MRI scans. Treatment options for central nervous system cysts vary depending on the size, location, and symptoms of the cyst, but may include observation, surgery, or endoscopic procedures to drain or remove the cyst.
Some common types of central nervous system cysts include:
1. Arachnoid cysts: These are flattened sacs that form between the layers of tissue that cover the brain and spinal cord (meninges).
2. Ventricular cysts: These are cysts that form within the ventricles, which are fluid-filled spaces within the brain.
3. Cerebral cysts: These are cysts that form within the tissue of the brain.
4. Spinal cysts: These are cysts that form within the spinal cord or along the spine.
5. Neurocysticercosis: This is a parasitic infection caused by the larvae of the pork tapeworm, which can form cysts within the brain and spinal cord.
While central nervous system cysts are generally not cancerous, they can still cause significant health problems if left untreated. It is important to seek medical attention if symptoms persist or worsen over time, as early diagnosis and treatment can help prevent complications and improve outcomes.
Note: Hematoma is a collection of blood outside the blood vessels.
Subdural effusion is a condition where there is an accumulation of fluid between the dura mater, the protective covering of the brain, and the skull. This fluid can be cerebrospinal fluid (CSF) or blood. The excess fluid can cause pressure on the brain, leading to various symptoms such as headaches, nausea, vomiting, and confusion.
There are several causes of subdural effusion, including:
1. Traumatic brain injury: A blow to the head can cause the veins in the dura mater to tear, leading to bleeding or fluid accumulation.
2. Infections such as meningitis or encephalitis: These infections can cause inflammation and fluid buildup in the dura mater.
3. Tumors: Both benign and malignant tumors can cause subdural effusion by obstructing the flow of CSF or by causing inflammation.
4. Hydrocephalus: This is a condition where there is an abnormal accumulation of CSF in the brain, leading to increased intracranial pressure and fluid buildup in the dura mater.
5. Spinal or cerebral vasculature disorders: Conditions such as stroke, aneurysm, or arteriovenous malformation can cause subdural effusion by disrupting the flow of blood or CSF.
Symptoms of subdural effusion can vary depending on the location and severity of the fluid accumulation. Common symptoms include:
1. Headache: This is the most common symptom, which can range from mild to severe.
2. Nausea and vomiting: Patients may experience nausea and vomiting due to the pressure on the brain.
3. Confusion and disorientation: Subdural effusion can cause confusion, disorientation, and difficulty with concentration and memory.
4. Weakness or numbness: Patients may experience weakness or numbness in the arms or legs due to the pressure on the brain.
5. Seizures: In some cases, subdural effusion can cause seizures.
Diagnosis of subdural effusion typically involves a combination of physical examination, imaging studies, and laboratory tests. Imaging studies, such as CT or MRI scans, are used to confirm the presence of fluid accumulation in the subdural space. Laboratory tests, such as electrolyte panels and blood counts, may be ordered to rule out other conditions that can cause similar symptoms.
Treatment of subdural effusion depends on the underlying cause and severity of the condition. In some cases, conservative management with supportive care, such as fluid and electrolyte replacement, pain management, and seizure control, may be sufficient. Surgical intervention may be necessary in more severe cases or if there is no response to conservative management.
Surgery for subdural effusion involves draining the excess fluid and repairing any underlying blood vessel ruptures or tears. In some cases, a shunt may be inserted to help drain excess fluid and relieve pressure on the brain. Postoperatively, patients may require close monitoring in an intensive care unit and may need to undergo rehabilitation to regain lost function and mobility.
Prevention of subdural effusion is challenging, as many of the underlying causes are unpredictable and unavoidable. However, prompt recognition and management of the condition can help prevent complications and improve outcomes. In some cases, prophylactic measures such as corticosteroid therapy or anticonvulsant medications may be used to reduce the risk of developing subdural effusion.
Overall, subdural effusion is a serious medical condition that requires prompt recognition and management to prevent complications and improve outcomes. A multidisciplinary approach involving neurologists, neurosurgeons, rehabilitation specialists, and other healthcare professionals may be necessary to provide comprehensive care for patients with this condition.
There are several types of spinal cord compression, including:
1. Central canal stenosis: This occurs when the central canal of the spine narrows, compressing the spinal cord.
2. Foraminal stenosis: This occurs when the openings on either side of the spine (foramina) narrow, compressing the nerves exiting the spinal cord.
3. Spondylolisthesis: This occurs when a vertebra slips out of place, compressing the spinal cord.
4. Herniated discs: This occurs when the gel-like center of a disc bulges out and presses on the spinal cord.
5. Bone spurs: This occurs when bone growths develop on the vertebrae, compressing the spinal cord.
6. Tumors: This can be either primary or metastatic tumors that grow in the spine and compress the spinal cord.
7. Trauma: This occurs when there is a direct blow to the spine, causing compression of the spinal cord.
Symptoms of spinal cord compression may include:
* Pain, numbness, weakness, or tingling in the arms and legs
* Difficulty walking or maintaining balance
* Muscle wasting or loss of muscle mass
* Decreased reflexes
* Loss of bladder or bowel control
* Weakness in the muscles of the face, arms, or legs
* Difficulty with fine motor skills such as buttoning a shirt or typing
Diagnosis of spinal cord compression is typically made through a combination of physical examination, medical history, and imaging tests such as X-rays, CT scans, or MRI scans. Treatment options for spinal cord compression depend on the underlying cause and may include medication, surgery, or a combination of both.
In conclusion, spinal cord compression is a serious medical condition that can have significant impacts on quality of life, mobility, and overall health. It is important to be aware of the causes and symptoms of spinal cord compression in order to seek medical attention if they occur. With proper diagnosis and treatment, many cases of spinal cord compression can be effectively managed and improved.
There are different types of hernias, including:
1. Inguinal hernia: This is the most common type of hernia, which occurs in the groin area when a part of the intestine bulges through a weakened area in the abdominal wall.
2. Hiatal hernia: This type of hernia occurs when the stomach bulges up into the chest through an opening in the diaphragm, which is the muscle that separates the chest from the abdomen.
3. Umbilical hernia: This type of hernia occurs near the belly button when a weakened area in the abdominal wall allows the intestine or other tissue to bulge through.
4. Ventral hernia: This type of hernia occurs in the abdomen when a weakened area in the muscle or connective tissue allows the intestine or other tissue to bulge through.
5. Incisional hernia: This type of hernia occurs through a previous surgical incision, which can weaken the abdominal wall and allow the intestine or other tissue to bulge through.
Hernias can be caused by a variety of factors, including:
1. Weakened abdominal muscles or connective tissue due to age, injury, or surgery.
2. Increased pressure within the abdomen, such as from heavy lifting, coughing, or straining during bowel movements.
3. Genetic predisposition, as some people may be more prone to developing hernias due to their genetic makeup.
Symptoms of hernias can include:
1. A bulge or lump in the affected area.
2. Pain or discomfort in the affected area, which may be worse with straining or heavy lifting.
3. Feeling of heaviness or discomfort in the abdomen.
4. Discomfort or pain in the testicles, if the hernia is in the inguinal region.
5. Nausea and vomiting, if the hernia is causing a blockage or strangulation.
If you suspect that you or someone else may have a hernia, it is important to seek medical attention as soon as possible. Hernias can be repaired with surgery, and prompt treatment can help prevent complications such as bowel obstruction or strangulation.
In addition to surgical repair, there are some lifestyle changes that can help manage the symptoms of hernias and improve overall health. These include:
1. Eating a healthy diet that is high in fiber and low in fat to promote digestive health and prevent constipation.
2. Staying hydrated by drinking plenty of water to help soften stool and prevent straining during bowel movements.
3. Avoiding heavy lifting, bending, or straining, as these activities can exacerbate hernias and lead to complications.
4. Getting regular exercise to improve overall health and reduce the risk of developing other health problems.
5. Managing stress and anxiety through relaxation techniques such as deep breathing, meditation, or yoga, as chronic stress can exacerbate hernia symptoms.
It is important to note that while lifestyle changes can help manage the symptoms of hernias, surgical repair is often necessary to prevent complications and ensure proper healing. If you suspect that you or someone else may have a hernia, it is important to seek medical attention as soon as possible to receive an accurate diagnosis and appropriate treatment.
Types of Ovarian Cysts:
1. Functional cysts: These cysts form during the menstrual cycle and are usually small and disappear on their own within a few days or weeks.
2. Follicular cysts: These cysts form when a follicle (a tiny sac containing an egg) does not release an egg and instead fills with fluid.
3. Corpus luteum cysts: These cysts form when the corpus luteum (the sac that holds an egg after it's released from the ovary) does not dissolve after pregnancy or does not produce hormones properly.
4. Endometrioid cysts: These cysts are formed when endometrial tissue (tissue that lines the uterus) grows outside of the uterus and forms a cyst.
5. Cystadenomas: These cysts are benign tumors that grow on the surface of an ovary or inside an ovary. They can be filled with a clear liquid or a thick, sticky substance.
6. Dermoid cysts: These cysts are formed when cells from the skin or other organs grow inside an ovary. They can contain hair follicles, sweat glands, and other tissues.
Symptoms of Ovarian Cysts:
1. Pelvic pain or cramping
2. Bloating or discomfort in the abdomen
3. Heavy or irregular menstrual bleeding
4. Pain during sex
5. Frequent urination or difficulty emptying the bladder
6. Abnormal vaginal bleeding or spotting
Diagnosis and Treatment of Ovarian Cysts:
1. Pelvic examination: A doctor will check for any abnormalities in the reproductive organs.
2. Ultrasound: An ultrasound can help identify the presence of a cyst and determine its size, location, and composition.
3. Blood tests: Blood tests can be used to check hormone levels and rule out other conditions that may cause similar symptoms.
4. Laparoscopy: A laparoscope (a thin tube with a camera and light) is inserted through a small incision in the abdomen to visualize the ovaries and remove any cysts.
5. Surgical removal of cysts: Cysts can be removed by surgery, either through laparoscopy or open surgery.
6. Medications: Hormonal medications may be prescribed to shrink the cyst and alleviate symptoms.
It is important to note that not all ovarian cysts cause symptoms, and some may go away on their own without treatment. However, if you experience any of the symptoms mentioned above or have concerns about an ovarian cyst, it is essential to consult a healthcare provider for proper diagnosis and treatment.
Some common examples of spinal cord diseases include:
1. Spinal muscular atrophy: This is a genetic disorder that affects the nerve cells responsible for controlling voluntary muscle movement. It can cause muscle weakness and wasting, as well as other symptoms such as respiratory problems and difficulty swallowing.
2. Multiple sclerosis: This is an autoimmune disease that causes inflammation and damage to the protective covering of nerve fibers in the spinal cord. Symptoms can include vision problems, muscle weakness, balance and coordination difficulties, and cognitive impairment.
3. Spinal cord injuries: These can occur as a result of trauma, such as a car accident or a fall, and can cause a range of symptoms including paralysis, numbness, and loss of sensation below the level of the injury.
4. Spinal stenosis: This is a condition in which the spinal canal narrows, putting pressure on the spinal cord and nerve roots. Symptoms can include back pain, leg pain, and difficulty walking or standing for long periods.
5. Tumors: Benign or malignant tumors can grow in the spinal cord, causing a range of symptoms including pain, weakness, and numbness or tingling in the limbs.
6. Infections: Bacterial, viral, or fungal infections can cause inflammation and damage to the spinal cord, leading to symptoms such as fever, headache, and muscle weakness.
7. Degenerative diseases: Conditions such as amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS) can cause progressive degeneration of the spinal cord nerve cells, leading to muscle weakness, twitching, and wasting.
8. Trauma: Traumatic injuries, such as those caused by sports injuries or physical assault, can damage the spinal cord and result in a range of symptoms including pain, numbness, and weakness.
9. Ischemia: Reduced blood flow to the spinal cord can cause tissue damage and lead to symptoms such as weakness, numbness, and paralysis.
10. Spinal cord infarction: A blockage in the blood vessels that supply the spinal cord can cause tissue damage and lead to symptoms similar to those of ischemia.
It's important to note that some of these conditions can be caused by a combination of factors, such as genetics, age, lifestyle, and environmental factors. It's also worth noting that some of these conditions can have a significant impact on quality of life, and in some cases, may be fatal.
There are several types of headaches, including:
1. Tension headache: This is the most common type of headache and is caused by muscle tension in the neck and scalp.
2. Migraine: This is a severe headache that can cause nausea, vomiting, and sensitivity to light and sound.
3. Sinus headache: This type of headache is caused by inflammation or infection in the sinuses.
4. Cluster headache: This is a rare type of headache that occurs in clusters or cycles and can be very painful.
5. Rebound headache: This type of headache is caused by overuse of pain medication.
Headaches can be treated with a variety of methods, such as:
1. Over-the-counter pain medications, such as acetaminophen or ibuprofen.
2. Prescription medications, such as triptans or ergots, for migraines and other severe headaches.
3. Lifestyle changes, such as stress reduction techniques, regular exercise, and a healthy diet.
4. Alternative therapies, such as acupuncture or massage, which can help relieve tension and pain.
5. Addressing underlying causes, such as sinus infections or allergies, that may be contributing to the headaches.
It is important to seek medical attention if a headache is severe, persistent, or accompanied by other symptoms such as fever, confusion, or weakness. A healthcare professional can diagnose the cause of the headache and recommend appropriate treatment.
Types of Hypothalamic Diseases:
1. Hypothalamic hamartoma: A benign tumor that develops in the hypothalamus and can cause a variety of symptoms such as seizures, obesity, and developmental delays.
2. Hypothalamic glioma: A malignant tumor that arises in the hypothalamus and can cause similar symptoms to hypothalamic hamartoma.
3. Hypothalamic malformations: Congenital abnormalities that affect the development of the hypothalamus, leading to various neurological symptoms such as seizures, intellectual disability, and behavioral problems.
4. Hypothalamic infarction: A condition where there is a lack of blood flow to the hypothalamus, leading to damage to the tissue and potentially causing a range of symptoms including stroke-like symptoms.
5. Hypothalamic lesions: Damage to the hypothalamus caused by traumatic brain injury, infection, or other factors, which can lead to a range of neurological symptoms.
Symptoms of Hypothalamic Diseases:
The symptoms of hypothalamic diseases can vary depending on the specific condition and the severity of the damage to the hypothalamus. Some common symptoms include:
* Seizures
* Headaches
* Vision problems
* Balance and coordination difficulties
* Weight changes (gain or loss)
* Sleep disturbances
* Mood changes (depression, anxiety)
* Behavioral problems (aggression, irritability)
* Intellectual disability
Diagnosis of Hypothalamic Diseases:
Diagnosing hypothalamic diseases can be challenging and may require a range of tests and evaluations. These may include:
1. Physical examination and medical history: A thorough evaluation of the patient's symptoms, medical history, and physical condition.
2. Imaging tests: Such as CT or MRI scans to visualize the brain and identify any structural abnormalities or lesions in the hypothalamus.
3. Blood tests: To check for hormone levels and other markers that can help diagnose specific conditions.
4. EEG and other neurological tests: To evaluate the patient's neurological function and identify any potential seizure activity or other abnormalities.
5. Genetic testing: If the condition is suspected to be inherited, genetic testing may be performed to identify mutations or variations in genes that can contribute to hypothalamic diseases.
Treatment of Hypothalamic Diseases:
The treatment of hypothalamic diseases depends on the specific condition and the severity of the symptoms. Some common treatments include:
1. Medications: Such as anticonvulsants, hormone replacement therapy, and pain management medications to control seizures, hormonal imbalances, and pain.
2. Hormone replacement therapy: To replace hormones that are deficient or imbalanced.
3. Surgery: May be necessary to remove a tumor or repair a structural abnormality in the hypothalamus.
4. Lifestyle modifications: Such as changes to diet, exercise, and sleep habits to manage symptoms and improve quality of life.
5. Rehabilitation therapy: To help regain lost functions and improve daily living skills.
Prognosis of Hypothalamic Diseases:
The prognosis for hypothalamic diseases varies depending on the specific condition and the severity of the symptoms. Some conditions may have a good prognosis with appropriate treatment, while others may have a poorer outcome. In general, early diagnosis and treatment can improve the chances of a better outcome.
Living with Hypothalamic Diseases:
Living with a hypothalamic disease can be challenging and may require significant lifestyle modifications and ongoing medical care. However, with the right treatment and support, many people are able to manage their symptoms and improve their quality of life. Some tips for living with a hypothalamic disease include:
1. Educate yourself about your condition and its management.
2. Work closely with your healthcare provider to develop a personalized treatment plan.
3. Make lifestyle modifications such as changes to diet, exercise, and sleep habits.
4. Join a support group to connect with others who are living with similar conditions.
5. Seek mental health support if needed to cope with the emotional impact of the condition.
In conclusion, hypothalamic diseases can have a significant impact on quality of life, but with early diagnosis and appropriate treatment, many people are able to manage their symptoms and improve their outcomes. It is important to work closely with a healthcare provider to develop a personalized treatment plan and make lifestyle modifications as needed. With the right support and resources, it is possible to live a fulfilling life with a hypothalamic disease.
Epidermal cysts are relatively common and can occur anywhere on the body, but they are most commonly found on the face, neck, torso, and arms. They are usually small, ranging in size from a pinpoint to a pea-sized bump, but they can sometimes grow larger.
Epidermal cysts are benign (non-cancerous) growths, and they typically do not cause any symptoms unless they become infected or rupture. In rare cases, epidermal cysts can become inflamed or infected, which can lead to redness, swelling, and pain.
Epidermal cysts are usually diagnosed by a dermatologist or other healthcare provider based on their appearance and location. In some cases, a biopsy may be performed to confirm the diagnosis. Treatment for epidermal cysts is usually not necessary unless they become inflamed or infected, in which case antibiotics or surgical drainage may be recommended.
It's important to note that epidermal cysts are different from sebaceous cysts, which are similar but occur in the deeper layers of the skin and are filled with a thick, cheesy material. Both types of cysts are benign and typically do not cause any symptoms unless they become infected or rupture.
Word origin: A combination of "fire" and "setting," referring to the act of intentionally starting a fire.
Example sentence: "The patient's history of firesetting behavior led the therapist to suspect that they may be suffering from pyromania."
There are several types of hydrocephalus, including:
1. Aqueductal stenosis: This occurs when the aqueduct that connects the third and fourth ventricles becomes narrowed or blocked, leading to an accumulation of CSF in the brain.
2. Choroid plexus papilloma: This is a benign tumor that grows on the surface of the choroid plexus, which is a layer of tissue that produces CSF.
3. Hydrocephalus ex vacuo: This occurs when there is a decrease in the volume of brain tissue due to injury or disease, leading to an accumulation of CSF.
4. Normal pressure hydrocephalus (NPH): This is a type of hydrocephalus that occurs in adults and is characterized by an enlarged ventricle, gait disturbances, and cognitive decline, despite normal pressure levels.
5. Symptomatic hydrocephalus: This type of hydrocephalus is caused by other conditions such as brain tumors, cysts, or injuries.
Symptoms of hydrocephalus can include headache, nausea, vomiting, seizures, and difficulty walking or speaking. Treatment options for hydrocephalus depend on the underlying cause and may include medication, surgery, or a shunt to drain excess CSF. In some cases, hydrocephalus can be managed with lifestyle modifications such as regular exercise and a balanced diet.
Prognosis for hydrocephalus varies depending on the underlying cause and severity of the condition. However, with timely diagnosis and appropriate treatment, many people with hydrocephalus can lead active and fulfilling lives.
This medical term is used to describe a specific type of hematoma, which is a collection of blood outside of blood vessels. This particular type of hematoma occurs in the space between the dura mater and the brain, and it develops over time. It can be caused by a blow or injury to the head, and it is more common in older adults due to the natural aging process affecting the elasticity of brain tissue.
The term 'chronic' is added to distinguish this type of hematoma from an acute subdural hematoma, which develops quickly and suddenly after a head injury. The symptoms of chronic subdural hematomas can be subtle and may not appear until days or weeks after the initial injury, making them more difficult to diagnose.
Chronic subdural hematomas are typically treated with surgery to drain the accumulated blood and relieve pressure on the brain. In some cases, a shunt may be placed to help drain excess fluid and prevent future bleeding.
Some common types of cerebellar diseases include:
1. Cerebellar atrophy: This is a condition where the cerebellum shrinks or degenerates, leading to symptoms such as tremors, muscle weakness, and difficulty with movement.
2. Cerebellar degeneration: This is a condition where the cerebellum deteriorates over time, leading to symptoms such as loss of coordination, balance problems, and difficulties with speech and language.
3. Cerebellar tumors: These are abnormal growths that develop in the cerebellum, which can cause a variety of symptoms depending on their size and location.
4. Cerebellar stroke: This is a condition where blood flow to the cerebellum is interrupted, leading to damage to the brain tissue and symptoms such as weakness or paralysis of certain muscle groups.
5. Cerebellar vasculature disorders: These are conditions that affect the blood vessels in the cerebellum, leading to symptoms such as transient ischemic attacks (TIAs) or strokes.
6. Inflammatory diseases: These are conditions that cause inflammation in the cerebellum, leading to symptoms such as tremors, ataxia, and weakness.
7. Infections: Bacterial, viral, or fungal infections can affect the cerebellum and cause a range of symptoms.
8. Trauma: Head injuries or other forms of trauma can damage the cerebellum and lead to symptoms such as loss of coordination, balance problems, and memory loss.
9. Genetic disorders: Certain genetic mutations can affect the development and function of the cerebellum, leading to a range of symptoms.
10. Degenerative diseases: Conditions such as multiple sclerosis, Parkinson's disease, and Huntington's disease can cause degeneration of the cerebellum and lead to symptoms such as tremors, ataxia, and weakness.
It's important to note that this is not an exhaustive list, and there may be other causes of cerebellar symptoms not included here. A healthcare professional can help determine the underlying cause of your symptoms based on a thorough medical history and examination.
Some common examples of cranial nerve diseases include:
1. Bell's palsy: A condition that affects the facial nerve, causing weakness or paralysis of one side of the face.
2. Multiple sclerosis: An autoimmune disease that damages the protective covering of nerve fibers, leading to communication problems between the brain and the rest of the body.
3. Trigeminal neuralgia: A condition that affects the trigeminal nerve, causing facial pain and numbness.
4. Meningitis: An inflammation of the meninges, the protective covering of the brain and spinal cord, which can damage the cranial nerves.
5. Acoustic neuroma: A type of non-cancerous tumor that grows on the nerve that connects the inner ear to the brain.
6. Cranial polyneuropathy: A condition where multiple cranial nerves are damaged, leading to a range of symptoms including muscle weakness, numbness, and pain.
7. Tumors: Both benign and malignant tumors can affect the cranial nerves, causing a variety of symptoms depending on their location and size.
8. Trauma: Head injuries or trauma can damage the cranial nerves, leading to a range of symptoms.
9. Infections: Bacterial or viral infections such as meningitis or encephalitis can damage the cranial nerves, leading to a range of symptoms.
10. Genetic disorders: Certain genetic disorders such as Charcot-Marie-Tooth disease can affect the cranial nerves, leading to a range of symptoms.
It's important to note that this is not an exhaustive list and there may be other causes of cranial nerve damage. If you are experiencing any symptoms that you think may be related to cranial nerve damage, it's important to seek medical attention as soon as possible for proper diagnosis and treatment.
There are several types of barotrauma that can occur in the human body, including:
1. Pulmonary barotrauma: This occurs when the air spaces in the lungs are subjected to sudden changes in pressure, leading to damage to the lung tissue and potentially causing pneumothorax (collapsed lung) or pneumomediastinum (air in the mediastinum).
2. Sinus barotrauma: This occurs when the sinuses are subjected to sudden changes in pressure, leading to damage to the sinus membranes and potentially causing bleeding or infection.
3. Middle ear barotrauma: This occurs when the eustachian tube, which connects the middle ear to the back of the throat, fails to equalize the pressure on both sides of the eardrum, leading to damage to the eardrum or middle ear bones.
4. Cerebral barotrauma: This occurs when the brain is subjected to sudden changes in pressure, potentially leading to damage to the brain tissue and other complications such as stroke or seizures.
Symptoms of barotrauma can vary depending on the location and severity of the injury, but may include:
* Chest pain or tightness
* Difficulty breathing
* Coughing up blood or froth
* Headache
* Dizziness or loss of consciousness
* Hearing loss or ringing in the ears
Treatment of barotrauma depends on the underlying cause and severity of the injury. In some cases, medical intervention may be necessary to manage symptoms and prevent further complications.
Meningocele can occur alone or as part of other congenital anomalies, such as spina bifida or encephalocele. It is usually diagnosed at birth and can be associated with other neurological problems, such as hydrocephalus (fluid accumulation in the brain) or spinal cord abnormalities.
Treatment for meningocele typically involves surgery to repair the defect and relieve any pressure on the brain or spinal cord. In some cases, meningocele may be associated with other congenital anomalies that require additional surgical interventions. With appropriate treatment, many individuals with meningocele can lead normal lives. However, in severe cases, meningocele can be associated with long-term cognitive and physical disabilities.
Arachnoid cyst
Absent tibia-polydactyly-arachnoid cyst syndrome
Central nervous system cyst
Cerebral shunt
Karin Muraszko
Craniopharyngioma
Trigeminal neuralgia
Gail Rosseau
Subdural hematoma
Differential diagnoses of anorexia nervosa
Chudley-Mccullough syndrome
Cerebellopontine angle
Antonio Pacchioni
Bobble-head doll syndrome
Hydrocephalus
Rex Lewis-Clack
Central nervous system disease
Tarlov cyst
Isadore Tarlov
Nervous system neoplasm
Dandy-Walker malformation
ZTTK syndrome
Dave Myers (presenter)
Perivascular space
Precocious puberty
List of diseases (T)
List of MeSH codes (C04)
Ruben Kuzniecky
Vestibular schwannoma
Macrocephaly
Autosomal dominant polycystic kidney disease
List of fetal abnormalities
Index of anatomy articles
Ventricular system
Wayne McCullough
Syringomyelia
Trendelenburg position
Blood-Spinal Cord Barrier
Diastematomyelia
ACMF
List of MeSH codes (C10)
Arachnoid Cysts | National Institute of Neurological Disorders and Stroke
Arachnoid Cyst Imaging: Practice Essentials, Radiography, Computed Tomography
Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts - PubMed
Arachnoid Cysts | Profiles RNS
Dermoid, Epidermoid and Arachnoid Cysts - Goodman Campbell
Retrocerebellar arachnoid cyst: treatment
Kaiden and the Arachnoid Cyst: Kaiden and the scared sister
Arachnoid cysts in tuberous sclerosis complex. | Brain Dev;36(9): 801-6, 2014 Oct. | MEDLINE | Biblioteca Virtual em Saúde
Nervous System Diseases | Neurologic Diseases | MedlinePlus
Neoplasia of the Nervous System | IVIS
A Visual Field Defect in a Patient With History of Seizures
Lymphedema-Distichiasis Syndrome - GeneReviews® - NCBI Bookshelf
Doctor | Upstate Patient Care | SUNY Upstate Medical University
A case of hydrocephalus confounded by suprasellar arachnoid cyst and concomitant reversible cerebral vasoconstriction syndrome ...
Brain Epidermoid Cyst (Epidermoid Tumor) Imaging: Practice Essentials, Computed Tomography, Magnetic Resonance Imaging
Fifteen-minute consultation: incidental findings on brain and spine imaging | ADC Education & Practice Edition
Biomarkers Search
Autosomal dominant polycystic kidney disease - About the Disease - Genetic and Rare Diseases Information Center
Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia - GeneReviews® - NCBI Bookshelf
Table of Contents - September 01, 1997, 18 (8) | American Journal of Neuroradiology
Possible Causes Of Tingling In Hands And Arms - Causes Of Tingling In Hands And Arms
Epilepsy and seizures | Emergency Medicine Journal
Medical Conditions & Diseases - Ask Me Help Desk
Minerva Pediatrica 2003 December;55(6) - Minerva Medica - Journals
Vestibular schwannoma | Radiology Reference Article | Radiopaedia.org
Architecture of arachnoid trabeculae, pillars, and septa in the subarachnoid space of the human optic nerve: anatomy and...
Automatically measuring brain ventricular volume within PACS using artificial intelligence | PLOS ONE
MeSH Browser
Middle crani1
- Most arachnoid cysts form outside the temporal lobe of the brain in an area of the skull known as the middle cranial fossa. (nih.gov)
Cerebrospinal fluid5
- An arachnoid cyst is a congenital lesion that develops due to abnormal duplication of arachnoid membrane adjacent to the brain and is filled with cerebrospinal fluid (CSF). (bmj.com)
- This rare cerebrospinal fluid-filled cyst develops on the surface of brain and between the cranial bases and usually shows up on the spinal cord and brain. (iloveindia.com)
- To describe the anatomy and the arrangement of the arachnoid trabeculae, pillars, and septa in the subarachnoid space of the human optic nerve and to consider their possible clinical relevance for cerebrospinal fluid dynamics and fluid pressure in the subarachnoid space of the human optic nerve. (bmj.com)
- The subarachnoid space of the human optic nerve is not a homogeneous and anatomically empty chamber filled with cerebrospinal fluid, but it contains a complex system of arachnoid trabeculae and septa that divide the subarachnoid space. (bmj.com)
- Asymptomatic patients with an enlarged sella turcica should have an air study to exclude an 'empty sella"syndrome, an anatomical entity in which the pituitary fossa is expanded and partially filled with cerebrospinal fluid owing to the arachnoid herniation, while the pituitary gland is compressed against the posterior rim of the fossa [3]. (bvsalud.org)
Hydrocephalus8
- Immediate intervention is necessary if the cyst is in a critical location causing hydrocephalus or if a large cyst is resulting in mass effect and brain herniation. (medscape.com)
- Kaiden is a little boy with an Arachnoid Cyst that has caused hydrocephalus. (hinshelwood.com)
- It has been a long slog from the 26th May 2010 when he had his Scan and we were told about the Arachnoid Cyst, the Hydrocephalus and we saw the scans. (hinshelwood.com)
- Obstructive hydrocephalus is a neurologic condition that has varied clinical and imaging presentations, as well as a multitude of congenital etiologies including aqueductal stenosis and less commonly arachnoid cysts. (scientificscholar.in)
- Suprasellar cysts in particular may cause obstructive hydrocephalus as well as endocrine dysfunction. (scientificscholar.in)
- Obstructive hydrocephalus most commonly results following infection and hemorrhage, but there exist a multitude of congenital etiologies including aqueductal stenosis and arachnoid cysts. (scientificscholar.in)
- Likewise, arachnoid cysts causing macrocephaly in infancy and obstructive hydrocephalus (pineal, posterior fossa cysts) may need addressing. (bmj.com)
- 8. Gradually Progressive Symptoms of Normal Pressure Hydrocephalus Caused by an Arachnoid Cyst in the Fourth Ventricle: a Case Report. (nih.gov)
Diverticula1
- in such cases, arachnoid cysts or arachnoid diverticula may be located subdurally or in the epidural space, respectively. (medscape.com)
Benign4
- Arachnoid cysts are benign cysts that occur in the cerebrospinal axis in relation to the arachnoid membrane and that do not communicate with the ventricular system. (medscape.com)
- Most brain cysts are benign (not dangerous) and do not change or grow over time. (goodmancampbell.com)
- A brain cyst is almost always benign liquid formation having different sizes, shapes and which are located between the brain tissues. (vsebolezni.com)
- Epidermoid cysts (also called epidermoid tumors) are benign congenital lesions of ectodermal origin. (medscape.com)
Size of the cyst4
- The location and size of the cyst determine the symptoms and when those symptoms begin. (nih.gov)
- The need for treatment depends mostly on the location and size of the cyst. (nih.gov)
- In addition to the size of the cyst on its growth affected by the presence of infection, chronic impairment of blood flow to the heart, autoimmune disorders (particularly multiple sclerosis). (vsebolezni.com)
- There are many nonspecific manifestations, but the nature of symptoms and their degree of manifestation will always depend on the size of the cyst. (vsebolezni.com)
Asymptomatic3
- Some clinicians advocate treating only patients with symptomatic cysts, whereas others believe that even asymptomatic cysts should be decompressed to avoid future complications. (medscape.com)
- While arachnoid cysts are mostly asymptomatic, they may present with neurological symptoms that vary depending on the location of the lesion. (scientificscholar.in)
- Arachnoid cysts are usually asymptomatic, and it is wise to adopt a conservative approach. (bmj.com)
Spinal11
- Arachnoid cysts are sacs filled with spinal fluid that are located between the brain or spinal cord and the arachnoid membrane, one of the three membranes that cover the brain and spinal cord. (nih.gov)
- Primary arachnoid cysts are present at birth and are the result of developmental abnormalities in the brain and spinal cord that arise during the early weeks of gestation. (nih.gov)
- Arachnoid cysts involving the spinal cord are rarer. (nih.gov)
- Arachnoid cysts around the spinal cord press parts of the spinal cord, or nerve roots, closer together. (nih.gov)
- If arachnoid cysts are not treated, they may cause serious, permanent nerve damage if the cyst(s) injures the brain or spinal cord. (nih.gov)
- So, more doctors are choosing to remove the membranes of the cyst with surgery, or to open the cyst so its fluid can drain into the spinal fluid and be absorbed. (nih.gov)
- Spinal arachnoid cysts are commonly located dorsal to the cord in the thoracic region. (medscape.com)
- Intradural spinal arachnoid cysts are secondary to a congenital deficiency within the arachnoidal trabecula, especially in the septum posticum, or are the result of adhesions resulting from previous infection or trauma. (medscape.com)
- Spinal arachnoid cysts are generally misdiagnosed, because symptoms are often nonspecific. (medscape.com)
- Dermoid cysts form from trapped skin cells during the development of the brain and spinal cord. (goodmancampbell.com)
- Cardiac defects, cleft palate, and spinal extradural cysts occur in some families. (arizona.edu)
Communicate with the ventricular system1
- A porencephalic cyst may communicate with the ventricular system or may be separated from the ventricular system by a thin tissue layer. (medscape.com)
Posterior2
- Epidermoid cysts located in the posterior fossa usually arise in the lateral subarachnoid cisterns, and they are rarely located in the brain stem. (medscape.com)
- 19. Disequilibrium in patients with posterior fossa arachnoid cysts. (nih.gov)
Symptoms8
- Most people with arachnoid cysts develop symptoms before the age of 20, and especially during the first year of life, but some people with arachnoid cysts never have symptoms. (nih.gov)
- Treating the symptoms of arachnoid cysts usually makes the symptoms go away or improve. (nih.gov)
- If the cyst is small, it does not disturb surrounding tissue, and is not causing symptoms, some doctors will decide not to treat it. (nih.gov)
- In fact, most cysts in the brain do not cause any symptoms and most of the time are found incidentally on imaging studies of the brain or spine (for example, a head CT or brain MRI done to look for something else. (goodmancampbell.com)
- Symptoms of cysts may not always be pronounced. (vsebolezni.com)
- Rarely, arachnoid cysts can cause symptoms due to raised intracranial pressure or due to mass effect on the underlying brain. (bmj.com)
- 17. Neurodevelopmental and Psychiatric Symptoms in Patients with a Cyst Compressing the Cerebellum: an Ongoing Enigma. (nih.gov)
- The most common symptoms are kidney cysts, pain in the back and the sides and headaches. (nih.gov)
Clinical4
- Consider participating in a clinical trial so clinicians and scientists can learn more about arachnoid cysts and related disorders. (nih.gov)
- Our study suggests that arachnoid cysts are part of the clinical spectrum of TSC and may be also present in TSC patients without other typical TSC brain lesions. (bvsalud.org)
- Clinical and radiological surveillance would be appropriate for large arachnoid, cysts causing subacute mass effect or cysts located on cortical surface. (bmj.com)
- 12. [Intracranial arachnoid cysts in the clinical and radiological aspect]. (nih.gov)
Type of cyst1
- This type of cyst may occur if the fetus receive less oxygen and the right amount of minerals in the womb. (vsebolezni.com)
Membrane4
- Microscopic examination shows that their walls are formed from a splitting of the arachnoid membrane, with an inner and outer leaflet surrounding the cyst cavity. (medscape.com)
- The most effective surgical treatment appears to be excision of the outer cyst membrane and cystoperitoneal shunting. (medscape.com)
- Arachnoid cysts form in the space between the arachnoid membrane and brain. (goodmancampbell.com)
- Arachnoid cysts can form wherever there is arachnoid membrane. (bmj.com)
Occur1
- Cysts can occur anywhere in the brain. (goodmancampbell.com)
Epidermoid cysts4
- Dermoid and epidermoid cysts are commonly removed surgically through a procedure such as neurosurgery or open microsurgery. (goodmancampbell.com)
- The usual locations of epidermoid cysts are the parasellar region and cerebellopontine angle, and it is less commonly located in sylvian fissure, suprasellar region, cerebral and cerebellar hemispheres, and lateral and fourth ventricles. (medscape.com)
- Patients with epidermoid cysts become symptomatic when the lesions compress the brainstem or stimulate cranial nerves. (medscape.com)
- On T1-weighted images, epidermoid cysts are generally slightly hyperintense or isointense relative to gray matter. (medscape.com)
Tumors1
- There is a classification of tumors depending on their location, for example, a cyst may be top or bottom. (vsebolezni.com)
Lesion1
- Differential diagnoses of an intracranial cystic lesion include porencephalic cyst, arachnoid cyst, schizencephaly, and ependymal cyst. (medscape.com)
Temporal1
- T2-weighted axial MRI scan brain showing an incidental left temporal fossa arachnoid cyst. (bmj.com)
Endoscopic1
- Surgical options include arachnoid cyst fenestration (open microscopic or endoscopic) or shunt drainage. (bmj.com)
Fenestration1
- 7. [A surgical fenestration of an arachnoid cyst in the cerebellomedullary cistern]. (nih.gov)
Surgical2
- Treatment of porencephalic cysts has included antiepileptic medication , such as valproate, [ 17 ] and surgical intervention. (medscape.com)
- Head trauma can cause cyst rupture leading to subdural hygromas or haematomas requiring surgical intervention. (bmj.com)
Cerebral1
- If the cyst formed in a certain part of the brain, then we can talk about a cerebral or intracerebral cyst. (vsebolezni.com)
Pituitary gland1
- it may be a cyst of the pituitary gland, and maybe If the cyst is located between the arachnoid sheath of the brain and its sheath - she arachnoid. (vsebolezni.com)
Diagnosis2
- Diagnosis usually involves a brain scan or spine scan using diffusion-weighted MRI (magnetic resonance imaging) which helps distinguish fluid-filled arachnoid cysts from other types of cysts. (nih.gov)
- Diagnosis of a cyst starts with a physical exam and medical history. (goodmancampbell.com)
Fluid-filled2
- A cyst is a fluid-filled sac (not a tumor) that can be found inside the brain. (goodmancampbell.com)
- Arachnoid cysts are thin walled and fluid filled central nervous system lesions that can result in mass effect on adjacent structures. (scientificscholar.in)
Anomalies1
- Other brain anomalies reported with the syndrome include frontal polymicrogyria and gray matter heterotopia, cerebellar dysplasia, ventriculomegaly, and arachnoid cysts. (medscape.com)
Cistern1
- T2-weighted sagittal MRI image (see next image for axial view) of the brain in a 28-year-old woman with an incidental finding of a superior cerebellar cistern arachnoid cyst (arrow). (medscape.com)
Neoplasms2
- A small number of arachnoid cysts are acquired, such as those occurring in association with neoplasms or those resulting from adhesions occurring in association with leptomeningitis, hemorrhage, or surgery. (medscape.com)
- A small number of arachnoid cysts are associated with neoplasms. (medscape.com)
Extradural1
- A cyst in this location is usually secondary to a congenital or acquired defect and is situated in an extradural location. (medscape.com)
Intracranial pressure1
- If the cyst rapidly increases, may increase intracranial pressure, which in turn will affect the appearance of an intense headache, the throbbing in my head. (vsebolezni.com)
Abnormal1
- There are several potential causes of brain cysts, including abnormal development, infection, infarction and trauma. (goodmancampbell.com)
Secondary2
- The radiologist needs to evaluate the brain structures for mass effect secondary to the arachnoid cyst, such as a subtle mass effect on a cranial nerve or a prominent mass effect resulting in brain herniation. (medscape.com)
- Secondary (acquired) cyst is the consequence of various abnormalities or negative side-effect to surgery. (vsebolezni.com)
Hemorrhage1
- Although rare, a brain cyst can rupture or hemorrhage and require immediate attention and possible surgery. (goodmancampbell.com)
Imaging4
- Often, the cysts are an incidental finding on magnetic resonance imaging (MRI). (medscape.com)
- Other procedures and tests may be needed to diagnose a cyst, including a detailed neurological exam , head CT or magnetic resonance imaging (MRI) scan. (goodmancampbell.com)
- With current excellent imaging technology, arachnoid cysts may be reported in 10% of MRI scans. (bmj.com)
- Surgery for arachnoid cysts causing epilepsy or behavioural/psychiatric disorders should be strongly supported by functional imaging. (bmj.com)
ADPKD2
- Three patients (25%) had two or more arachnoid cysts , of whom two also had ADPKD . (bvsalud.org)
- Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. (nih.gov)
Shunt1
- Arachnoid cysts are usually treated by draining the cyst of CSF and placing a shunt , a permanent tube that drains the CSF and directs it elsewhere to be absorbed. (goodmancampbell.com)
Seizures2
- If you have a brain cyst and develop a sudden headache with vomiting or seizures, you should seek immediate medical attention. (goodmancampbell.com)
- [ 1 ] This patient's cyst appeared to be either congenital or at least longstanding, based on her history of seizures at a young age. (medscape.com)
Tumor1
- The tumor appears as a result of inflammation of the meninges, brain injuries, or high pressure liquid accumulation, and can be diagnosed, for example, Livorna cyst occurs in about 4-5% of the population, but only two people out of ten has a marked occurrence of the disease. (vsebolezni.com)
Congenital or acquired1
- Retrocerebellar arachnoid livornaa cyst of the brain has a congenital or acquired form. (vsebolezni.com)
Cerebellum1
- The name comes from the localization of the cyst, that is associated with the cerebellum. (vsebolezni.com)
Commonly located1
- The cysts are commonly located within the substance of the pineal gland unlike arachnoid cysts that are located outside. (bmj.com)
Scans2
- With CT scans, the differentiation between arachnoid cyst and epidermoid cyst may be difficult. (medscape.com)
- this characteristic makes their differentiation from arachnoid cysts difficult on CT scans, but they are easily differentiated by MRI. (medscape.com)
Trauma1
- The cyst appears on a background of inflammation from infection, after trauma and mechanical damage. (vsebolezni.com)
Males1
- Males are four times more likely to have arachnoid cysts than females. (nih.gov)
Prevalence1
- The purpose of this study was to assess the prevalence and characteristics of arachnoid cysts in a large cohort of TSC. (bvsalud.org)
Malformations1
- 11. Intracranial cavernous malformations and skin angiomas associated with middle fossa arachnoid cyst: a report of three cases. (nih.gov)
Characteristics1
- Development retrocerebellar cyst of brain in an adult has its own characteristics. (vsebolezni.com)
Patients2
- Arachnoid cysts have been reported in two TSC patients to date. (bvsalud.org)
- We performed a review of brain MRIs of 220 TSC patients searching for arachnoid cysts . (bvsalud.org)
Genetic1
- A genetic link to arachnoid cysts has been described. (medscape.com)
Optic1
- The subarachnoid space of the human optic nerve contains a variety of trabeculae, septa, and stout pillars that are arranged between the arachnoid and the pia layers of the meninges of the nerve. (bmj.com)
Typically3
- These cysts typically appear in children. (goodmancampbell.com)
- These cysts typically appear in adults, as they are slow growing. (goodmancampbell.com)
- MRI typically reveals a brain cyst with a well-defined border, with a white matter lining with or without gliosis. (medscape.com)
Meninges1
- The arachnoid sheath is included in the conglomerate of the three meninges, which are located between the soft deep brain lining and solid surface shell. (vsebolezni.com)
Nerve1
- Hemorrhagic arachnoid cyst with third nerve paresis: CT and MR findings. (ajnr.org)