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BRAIN TUMORS IN CHILDREN

"I am truly sorry, but your child has a brain tumor..."

 The World of Childhood Brain Tumors has no "Welcome" sign leading into it.

No matter what anyone says to minimize the situation, this statement is the most painful sentence a human can hear. The combination of fear, shock, pain is much to bear.

"To see such innocence, so roughly shaken by this terrible trial, at such a young age, is nothing short of incomprehensible." I still hear this sentence, uttered by a visibly shaken parent. Instead of my becoming more routine and distant, the visceral terror that it engendered in me (the supposed all- knowing physician/advisor), the delivery of such information has grown more and more difficult, even personal. I watch my own small children grow and develop. As a physician, one realizes more than ever, there is no place for impersonal behavior when caring for the children who are afflicted by a brain tumor, benign or otherwise--their families as well. No amount of experience or training can help one to ease or minimize the situation.

When we discuss special areas such as:

     
  • Outcome: Does "excellent long-term results" mean a ten-year survival for a 3-year old-- your child living long enough to be frustrated by death at the age of thirteen? We parents think only of 50 and 60 year plans. Five and ten-year plans are unacceptable. We want to know that our grandchildren will not live to see their parents die at a young age.
  • Quality of life: Does that mean that a 5-year old child will have no hair, be skinny and slow to walk and play with his friends and classmates? How can we parents bear to live through the process of trying to give our child a childhood instead of a world of I.V. tubes, doctors who speak of life-and-death, hospital corridors and toys that our children will never play with?
  • Doctors: Who are they? Can we do anything to keep them human, warm, and caring for our child? How do we deal with our own resentment for the fearful news, difficult therapies and their human frailty? How do we keep our child happy to see them? Most children cringe at the mere mention of visiting a doctor-with-a-shot-to-give, or a visit to the dentist with his drills and instruments?
  • Hospitals: How do we keep these innocents away from such large and frightening monoliths?
  • We parents: How can we possibly bear all of this without frightening our little, loving child?
  • Hope: Yes, there IS hope! God and goodness are your guide. Your child is truly a precious gift. No matter what cards we are dealt, a child's joy and innocence are somehow never lost. In the worst of times, a child's pain often becomes the parent's teacher. And, when we expect the best for our children, we often get it despite all odds.

THE BIOLOGY OF CHILDHOOD BRAIN TUMORS

Pediatric brain tumors are different
Most frequently, they come from "young" cells. These are cells that are still developing ("immature" or "primitive" cells) and have not reached full maturity. They are developing at the same time as the child is developing. If one looks at the way a normal cell matures from its very beginning as a "primitive" brain cell (a precursor) through its stages of normal development, towards becoming an adult cell type, one can start to understand the logic of the progression of tumor types in children.

A diagrammatic representation of the manner in which brain cells develop from the embryo to the adult is under constructiion. It will be posted soon.

For every normal cell type, there is a corresponding tumor that can arise from it. Thus, there is the primitive neurectodermal tumor (PNET), the medulloblastoma, the astroblastoma, the neuroblastoma, the astrocytoma, the gangliocytoma/neurocytoma, the ependymoma and so on.

There are also other unusual tumors such as the teratoma, the pinealblastoma, the esthesioneuroblastoma, etc. There are also other tumors thay come from non-brain origins such as the pituitary tumors, teratomas, meningiomas, the skull bone tumors, and blood vessel tumors such as the hemangioblastoma or cavernous angioma.

Children commonly have brain tumors such as the PNET, medulloblastoma, various embryonic tumors and unusual tumors of the developing brainstem, hypothalamus and optic nerves (juvenile pilocytic astrocytomas, teratomas, etc.) There are variations of these tumors and they are rare as well as difficult to understand.

Parents and children should ask as many questions as possible. The questions can help reach level of comfort confident that the problem is clearly comprehended. Knowledge of the expected and the potentially unexpected will allow you to guide your child through the process of battle against their brain tumor. No matter how harried, tired or busy your surgeon and doctors might seem, it is important to understand the problem at hand fully. This will make the efforts of all involved more effective. More often than not, knowledge helps us cope with the developing situation better.

The most important point is that some of these tumors hold the promise for a true and complete cure! There is nothing more satisfactory than the complete removal of a dreadful sounding cerebellar microcystic astrocytoma or a hemangioblastoma. Families soar from the depths of despair to the heights of sublime elation when the smiling surgeon comes to the waiting room after a difficult surgery. The surgeon may not look tired at all. The smile-on-his-face says that he has just had the privilege of completely removing a tumor!

MEDULLOBLASTOMA

This tumor is probably the most common tumor of children. It arises from one of the "junior" cells of the developing brain, called the medulloblastoma. This tumor almost always grows in the middle of the cerebellum (the balance part of the brain, in the back, behind the brainstem). More often than not, small children are found to have the tumor only after it has caused secondary problems relating to blockage of the normal flow of cerebrospinal from the ventricles to the drainage system located along the outer surface of the brain (Obstructive Hydrocephalus). This results in headaches, visual problems, and decreased alertness. Often, parents will notice "sundowning", (the eyes are "stuck" in the downward gaze position) of the baby's eyes, due to local pressure on one of the brain's centers for eye control.

EPENDYMOMA

The ependymoma arises from the cells that line the internal surfaces of the brain. These cells line the fluid spaces of the brain (ventricular system) and are relatively few in number. Some of these cells are quite specialized, having little frond-like protruberances that move the cerebrospinal fluid as it permeates into the brain from the ventricular system and back again.

These tumors are rare. They are usually found on the internal surfaces of the brain and spinal cord, such as the fourth ventricle of the brain (in the back, inside) and within the central canal of the spinal cord. Occasionally they grow just beneath the surface of the lateral ventricles (called "subependymoma").

Although these tumors are capable of malignant behavior, they are almost always benign. Surgical removal often leads to a cure, especially when the tumor arises right from the surface to the fluid spaces of the brain and grows into the ventricles, an "exophytic" growth, allowing for complete removal.

If you or yours has this tumor, be confident that your future holds promise.

CEREBELLAR ASTROCYTOMA

This tumor is quite cureable. The small cyst version is one that, when surgically removed, is gone for good. Forget about all the fears, just thank God that your child will do well. Even if the MRI or CAT scan shows a large cyst with surrounding tumor or a tumor "nodule" in the wall of the cyst, the surgery can go well. When the tumor is the more aggressive type, the outcome deplends on the grade/size of the tumor.

TREATMENT OF CHILDHOOD BRAIN TUMORS

The treatment of these tumors usually include a combination of approaches, each tailored to deal with the problems that children are presented with:
     
  1. Surgery:- In some cases the definitive treatment is surgery. In most, however, surgery serves as a temporizing measure that will keep a child out of trouble for long enough to get through definitive therapy that will hopefully eliminate of the tumor. Brain surgery is usually the easiest part of a child's treatment.
  2. Shunting:- Quite often (e.g. medulloblastomas) childhood tumors present the blockage of the fluid spaces of the brain, (obstructive hydrocephalus). In Shunting, a thin silastic tube (the shunt) is placed into the fluid spaces of the brain, passed under the skin into the child's tummy where the fluid is absorbed.
  3. Chemotherapy:- Unfortunately, chemotherapy is the hard part of brain tumor treatment. It is only required for the more aggressive tumors. As a rule, chemotherapy should be even more aggressive than the tumor itself. The trials which are imposed both on the child and parents are legion. Bravery and an unremitting attitude of hope are required by all involved.
  4. Radiation:- Because the developing brain of a child is so very sensitive to radiation therapy, it is deliberately limited. The irony of effective radiation therapy is that when it works well, the brain damage it causes might exceed that done by the original tumor. More often than not, your doctor will recommend that if any radiation is to be given, it should be held off until the child has grown older and the brain has sufficiently matured.
The Good News is that REAL HOPE exists. Long term results are becoming more and more common, some children surviving fifty years and beyond. This has become especially true with the wonderful improvements in chemotherapy and surgical techniques. The promise of cures for difficult tumors is becoming a reality to more families than ever before.




Post a Question/Comment:

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I was first diagnosed at age 7 with a Grade I Astrocytoma in the fourth ventricle (1972). My doctor performed surgery to locate the tumor and then used radiation to shrink the tumor due to CSP Blockage. A shunt was implanted. Presently I have a second shunt due to unrelated head trauma. I am beginning to experience short term memory loss at age 46. Has anyone in the medical field, an individual, or caretaker experienced similar decline in mental alertness?

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my nephew is 8 years old.hediagnose with who grade 4 tumor in 2008.surgery , chemo and radiation already done.but he again diagnse with 3 cm tumor in same location?doctors said no to tratments.what we can do further to save him?

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im currently 16 years old and i was diagnosed with a brain tumor in march of 2010 .my surgeon told me that i had to go in brain surgery in may.it was something to think about i mean thats a little to much for a 16 year old but all i could do is think about god in how good he is i prayed in prayed and on may the third my prayers were answered jesus stayed with me in helped me through my surgery .it was done at johns hopkins hospital by dr.E.Ahn .im in wonderful conditon with no side effects as far as medication i take seizure medicine because my tumor caused me to have seizures also trauma to the brain can to .So i share my story to tell you that you think your going through something but its always someone going through something worse .so have faith stay strong in god will help you move along . the type of tumor i had was a astrocytoma grade 2(isaih 41:10)do not fear nor be dismayed for i am your god i will strenghen you in help you i will uphold you with my righteous right hand...tell the devil you though i was broken but i was just bruised !!!! stay strong

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Brain stem tumor (8/15/2010)
My 24 month old son has been diagnosed with a brain stem tumor. His Dr`s have said it is inoperable and can`t even do a biopsy. Looking for anyone who has had any experience of this.

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Neurocytoma (8/5/2010)
Sorry, this neurocytoma of the brain stem has been found in my 4 year old granddaughter. As much as could was removed. Will wait until she is older or what is left starts to grow substantially to start radiation and chemo.

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What info do you have on this? We have been told a neurocytoma is rare and even rarer to be in the brain stem?

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Both my sons have been diagnosed with anterior thalamic brain tumours, considered to be inoperable. We are waiting for our 11 yr olds next MRI to see how it and if it's growing.He has previously been diagnosed with Autism because of his symptoms, which now we are sure are more to do with the tumour. Does anyone out there know of any neurosurgeons willing and capable of doing surgery in the Thalamus?
Please help. thanks

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my son who was 2yrs 3 mths recently passed away after being diagnoised with a.t.r.t. and now its been said the one of his chemo drugs was the cause of his body shutting down as a m.r.i five days before showed now progresson of tumor, can methatrexate of been the cause. donna.

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anything please help advise someone that has been there

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brain tumor (4/4/2010)
I need some info on long term mental effects of frontal lobe brain tumor surgery, my son is suffering from extreme mental difficulties, 25 years after his surgery. Thanks to anyone who has info!

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i nedd some information about desmopl inf astrocytoma grade II
My daughter is 8 y old.
thank you so much.

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Tumors/Tumours (2/12/2010)
how do you spell it? Some people spell without a u some spell with?
Im confused :S

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