Meningioma

Il meningiomas is a brain tumor, usually benign which concerns the meninges, but it can also involve surrounding nervous tissue through compression. It's worth remembering how the meninges are structured. 

What are the meninges like?

The meninges are membranes that surround the brain and spinal cordThey are made up of three layers, going from the inside out:

  • pious mother, where blood vessels carry nourishment to the surface of the central nervous system
  • arachnoid
  • dura mater, within which blood vessels supply the skull

Classification of meningiomas

The World Health Organization has classified meningiomas by identifying 15 types based on the morphology of the cells that compose them (histological subtypes):

  • Grade I Benign
  • Grade II Atypical, which grows more rapidly and can expand into the brain. If atypical, the cerebral meningioma can reform more easily.
  • Grade III Malignant, characterized by even faster development and more marked cellular abnormalities. It has an even greater chance of spreading and recurring.

The risk factors

Some categories of subjects are at greater risk of developing a meningioma, which occurs more frequently in women (2 times more than men) and in general in people between 30 and 70 years. It is precisely the higher incidence in female subjects that has made scientists focus their attention on the relationship between brain meningioma and hormonesEstrogens, progesterone, and androgens have been detected in some of these tumors, and their development is also linked to the menstrual cycle, pregnancy, and breast cancer. It should be noted, however, that the risk of diagnosing a malignant meningioma is three times higher in men than in women. Meningioma is rarer in children, although a link between this tumor in pediatric age and radiation exposure has been observed in some cases. ionizing. Finally, the role of the neurofibromatosis type 2, a genetic disorder that increases the risk of developing malignant or multiple meningiomas. Meningiomas are not hereditary, but can become hereditary as a consequence of this disorder. 

Meningioma: symptoms and types

Meningioma can cause symptoms such as:

  • headache
  • convulsions
  • mood and behavioral disorders
  • drowsiness
  • confusion
  • progressive focal neurological deficit
  • hearing loss or tinnitus
  • vision disorders
  • muscle weakness
  • nausea
  • vomiting

 

Depending on the location of the meningioma, it is identified with a specific typology, which in turn can manifest itself with characteristic symptoms:

  • cavernous sinus meningioma, in the venous plexus that drains venous blood from the brain to the heart
  • cerebellopontine angle meningioma, near the lateral margin of the cerebellum
  • meningioma of the cerebral convexity, on the brain surface just under the skullcap, which can lead to headaches, seizures, neurological deficits
  • meningioma of the foramen magnum or foramen magnum
  • intraorbital meningioma, which can cause increased pressure inside the orbit and consequently the protrusion of the eyeballs and, in the most serious cases, loss of vision 
  • intraventricular meningioma, in the cavities where the cerebrospinal fluid passes. If it is blocked, it can develophydrocephalus obstructive, with headache, dizziness and altered mental functions
  • olfactory groove meningioma, along the nerves that connect the brain and nose and allow us to perceive smells. If the compression on the nerves is intense, loss of smell and vision can occur.
  • parasagittal and falx meningioma, statistically the most common, which can present with alterations in thinking and memory, convulsions, numbness of the lower limbs
  • petrous rock meningioma, the part of the temporal bone where the organs responsible for hearing are stored
  • posterior fossa meningioma, in the back of the brain. This type can cause hearing loss, balance problems, and coordination.
  • sphenoid meningioma, near the sphenoid bone, which can manifest with vision problems, facial numbness, and seizures
  • spinal meningioma, located in the spine, linked to possible back and limb pain
  • suprasellar meningioma, in the area where the pituitary gland is located, which can cause vision problems
  • tentorial meningioma, at the connection point between the brain and the brainstem

Meningioma: from diagnosis to surgery

It is not easy to recognize the symptoms of a cerebral meningioma, which can develop very slowly and is not characterized by such specific symptoms. The most commonly used tools are: computed tomography , magnetic resonance, although sometimes the only method to obtain a certain diagnosis is the biopsy performed by the neurosurgeonThe timing of diagnosis is very important: the younger the subject, the more positive the prognosisAlthough meningioma usually does not affect life expectancy (when benign), it can affect quality of life if symptoms are severe. It is therefore important to identify the right treatment. Since cerebral meningioma usually has a specific extension, Complete surgical removal is the best optionThe surgery is performed with a craniotomy to access the tumor, which is removed along with the fibers that connect it to the coverings of the brain and bones. Naturally, the possibility of surgery must be carefully evaluated, based on the individual patient's situation. If the meningioma cannot be surgically removed, the radiotherapy can be considered an alternative. Is there a pharmacological cure for meningioma? Actually, no, although research has evolved to achieve chemotherapeutic agents more targeted to treat the malignant tumor. In some cases, meningioma manifests itself with calcified, or ossified, elements: the calcific meningioma It is more common in older people and in general it does not need to be treated

Dr. François LECHANOINE

Senior Consultant Neurosurgeon, Specialist in minimally invasive endoscopic brain, spinal, and pediatric surgery at the NeuroNEC International Center in San Marino, which coordinates surgical activity between San Marino, Milan, Naples, and France.


Secretariat: open from Monday to Friday from 09:30 to 13:00 and from 15:00 to 18:00

 348 916 3317

Studies Program: San Marino – Milan
 

Related post

ventricular dilation

Hydrocephalus

With the term hydrocephalus the accumulation of is identified cerebrospinal fluid (or liquor) in the cerebral ventricles, which consequently they increase in volumeThe name of the pathology, deriving from the Greek, literally means “water in the head”.

What is liquor used for?

The cerebrospinal fluid, which surrounds the brain and spinal cord, is actually very similar to water. This fluid plays a fundamental and multifaceted role:

  • protects the spinal cord and brain from possible trauma
  • brings nutrients to the brain and eliminates harmful ones
  • balances intracranial and intravertebral pressure variations
hydrocephalus with ventricular dilation

Hydrocephalus: the causes

Among the most common causes of hydrocephalus are: cerebral hemorrhages (related to aneurysm), brain tumors, trauma, meningitis and infections, hemorrhagic complications in premature infantsMore rarely it can be considered a hereditary pathology, but it can be linked to pathologies of fetal development, such as spina bifida and encephaloceleThe most affected subjects are children (congenital hydrocephalus) and adults over 60 years old (normal pressure hydrocephalus)

Hydrocephalus and symptoms by age group

The symptoms of hydrocephalus vary depending on the patient's age:

  • neonate: abnormal increase in head circumference, tense and swollen fontanel, thin and taut scalp skin with prominent veins, separation between the skull bones, vomiting, irritability, downward gaze deviation (setting sun sign), loss of appetite, drowsiness
  • child: abnormal increase in head circumference in the first year of life, headache, vomiting, nausea, fever, visual disturbances (double vision and dimming), irritability, drowsiness, loss of balance and coordination, delay in walking and speaking, lack of concentration, character disorders, loss of sensory and motor functions, epileptic seizures, loss of appetite
  • healthier skin : headache, difficulty waking up and staying awake, lack of balance and coordination, urinary incontinence, vision problems, cognitive impairments that impair intellect and work activities
  • adult and elderlyGait disturbances, urinary incontinence, foot dragging, memory loss, dementia. The latter must be carefully investigated, as it is necessary to distinguish a symptom of normal pressure hydrocephalus from one of Alzheimer's disease.

Hydrocephalus: diagnosis and treatment

A thorough examination by your primary care physician and a complete neurological exam are the first steps to reaching a definitive diagnosis of hydrocephalus. Depending on the patient's age, the instrumental tests to be performed are: Ultrasound for newborns, brain MRI for children, brain CT or MRI for young people, adults and the elderlyTreatment is determined based on the causes of hydrocephalus, the severity of the condition, and the patient's condition. If hydrocephalus is caused by a tumor or malformation, it can be intervene directly on the cause. It is also possible drain the fluid elsewhere, through a valve, specially implanted just under the hair or behind the ear, and two cathetersThis instrument is constantly in operation and must remain in that location for its entire life. Alternatively, a reset operation can be performed. third ventriculostomy: the procedure, performed with the aid of an endoscope that allows internal visualization, opens a new passage for the cerebrospinal fluid on the floor of the third ventricle.

Recovery and life expectancy

Immediately after any surgical procedure, neurological functions should be measured and compared with those present before the operation. If the symptoms persist, a specific rehabilitationIf the patient has had a drainage shunt implanted, it is necessary constantly monitor the valve's operation via CT or MRI of the brain, as it should be check the positioning of the catheters with abdominal X-rays and ultrasound. It is essential to contact your doctor promptly if you experience pain, redness, tenderness, or swelling in the incision area or along the tube; drowsiness; irritability; fever; nausea; vomiting; headache; double vision; abdominal pain; or previously experienced neurological symptoms. If the valve malfunctions, causing the recurrence of hydrocephalus symptoms, replacement is possible, which is generally curative. The prognosis is strictly linked to the origin of the hydrocephalus, symptoms, and response to treatment. Consequently, It is very difficult to make a prediction for the patient's recovery. A weighty element in this path is the timeliness, both in diagnosis and treatment. If left untreated, congenital hydrocephalus unfortunately does not have a long life expectancy: approximately 4 years.