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Dr. Sarang Rote

Best Neurosurgeon in Pune

Dr. Sarang Rote is a Consultant Neurosurgeon & Neurointerventionist in Pune. He had very well focused training from specialty-specific Legends in Neurosurgery as well as with new generation Neurosurgeons around the world. He is trained in Neurointervention to form the pioneers of Neurointervention and many others. Also, he is well trained in the use of all-new advanced minimal invasive modalities, and technology. His area of interest are-

Cerebrovascular diseases for which he offers microscopic cerebrovascular neurosurgery as well as endovascular neurosurgery i.e. Neurointervention.
Skull base tumors & other lesions for which he offers microscopic as well as endoscopic skull base neurosurgery.
Stroke intervention & surgery.


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This is neurosurgery in children, and requires dedicated paediatric neurosurgeons with experience of operating on the developing nervous system working in close collaboration with paediatricians to achieve the best outcome for each child.  The London Neurosurgery Partnership has assembled just such a group.

Although brain tumours are rare in childhood, they are now the commonest solid cancer seen in children in the UK. There are 300 new cases in the UK every year and thanks to ongoing research, advances in both survival and quality of life continue.

 

Symptoms of Tumours
Tumours can present with a variety of symptoms, partly depending on the child’s age.  These symptoms include headaches, usually early morning, nausea and vomiting, fits or seizures, focal neurological deficit (weakness of limb or numbness), balance problems, increasing head size (babies from 0-18 mths), failure to put on weight and regression of milestones.
 
Investigation
If there is any question of a neurological problem in a child then a CT or MRI scan is mandatory. For babies the scan can be done under oral sedation. Beyond six months children will need a general anaesthetic (GA) for a scan and from 6-12 years old one may be able to MRI the child without any sedation or GA.
 
Treatment
Following admission to a neurosurgical unit all children must have a brain and spine MRI and blood should be sent for tumour markers. Steroids may be commenced to reduce swelling around the tumour and any hydrocephalus treated (by shunt or ventriculostomy or removal of tumour).All cases should be discussed with an oncologist and a plan should be made for excision or biopsy of the tumour.  Occasionally some tumours may be treated with chemotherapy or radiotherapy as a first line.

 

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The role of surgery may be diagnostic or therapeutic. Some patients may not be suitable for surgery.The location and extent of a tumour may make it unsuitable for a removal, in which case a biopsy may be performed to confirm the diagnosis. A biopsy removes a small piece of the tumour so it may be examined under the microscope.  When performing a biopsy we always use image guidance or a stereotactic frame as it is undoubtedly the safest way to perform a brain biopsyIf the tumour is in a relatively "silent" part of the brain or if it so large that it is causing symptoms or raised pressure in the brain, it may be debulked. The aim is to safely reduce the volume of the tumour. A craniotomy is performed with image guidance or with the help of the stereotactic frame. For primary malignant tumours of the brain we are able to use the latest tumour fluorescent labelling techniques (Gliadel©) to ensure the most effective possible tumour removal and instil intratumoural chemotherapy (Gliadel Wafers©) at the time of surgery if possible.

Brain Tumours can be divided into primary brain tumours (those that arise from the brain itself) and secondary (those that spread from a cancer somewhere else in the body).  The latter are more common.  Primary Brain Tumours almost never spread out from the central nervous system.

There are between 5-15 primary brain tumours per 100,000 population. This accounts for 5%-10% of all cancers in all age groups and probably 30%-40% of tumours in children.

It is now well recognised that patients with brain tumours (and their family) do best if managed by a group of doctors both medical and surgical who have a particular interest in the management of brain tumours.  This is known as Tumour Multidisciplinary Team (MDT).  As a group of neurosurgeons committed to the best outcome for their patients, we at the London Neurosurgery Partnership have come together with the doctors at Leaders in Oncology Care to provide just such a group.  As a result all patients with brain tumours receive highly individualised care that delivers not only the best treatment possible for the patient but treatment that is appropriate to the patient’s and family’s psychological and emotional needs.

 

Symptoms of Brain Tumours

 

Tumours usually present in one of three ways: headaches (54%), progressive neurological deficit (68%) or seizures (26%).

The headaches are related to raised pressure inside the brain. The classical description is one of early morning headaches, often over the forehead, which is present when the person wakes up. The headache usually settles by afternoon. Many patients also complain of nausea or vomiting.

Any neurological deficit will depend on the site of the tumour. The commonest deficit seen is a weakness (frontal tumour); some patients may have numbness (parietal tumour), problems with speech (dominant temporal tumour), visual problems (temporal, parietal or occipital tumour) or a change in personality (frontal tumour). Certain tumours present in a very specific fashion, i.e. endocrine problems with a pituitary tumour.

Seizures (epileptic fits) occurring for the first time in an adult must be investigated with an urgent scan. The types of fits seen in patients with tumours varies from classical grand mal seizures where the patient loses consciousness, shakes, may be incontinent and tongue bites, to focal seizures which may cause a temporary loss of function. In patients with a tumour in the movement area they may lose movement in one arm for a short period of time which then spontaneously recovers.

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