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Neuroblastoma is a form of cancer that starts in certain types
of very primitive developing nerve cells found in an embryo or fetus.
(The term neuro
indicates "nerves," while blastoma
refers to a cancer that affects immature or developing cells). This
type of cancer occurs in infants and young children. It is rarely found
in children older than 10 years.
In order to understand neuroblastoma, it helps to know
something about the normal structure and function of the sympathetic
nervous system.
About the sympathetic nervous system
The nervous system consists of the brain, spinal cord, and the
nerves that reach out from them to all areas of the body. The nervous
system is essential for thinking, sensation, and movement, among other
things.
Part of the nervous system also controls body functions we are
rarely aware of, such as heart rate, breathing, blood pressure,
digestion, and other functions. This part of the nervous system is
known as the autonomic
nervous system.
The sympathetic
nervous system is a part of the autonomic nervous system.
It includes:
- nerve fibers that run along either side the spinal cord
- clusters of nerve cells called ganglia (plural of ganglion)
at certain points along the path of the nerve fibers
- nerve-like cells found in the medulla (center) of the
adrenal glands. The adrenals are small glands that sit on top of each
kidney. These glands make the hormone adrenaline.
The main cells that make up the nervous system are called neurons. These
cells communicate with other types of cells in the body by releasing
tiny amounts of chemicals (hormones). This is important, because
neuroblastoma cells often release certain hormones that can cause
symptoms (see the section, "How
is neuroblastoma diagnosed?").
How neuroblastomas grow
Neuroblastomas are cancers that start in early nerve cells of
the sympathetic nervous system, so they can be found anywhere along
this system.
A little more than 1 out of 3 neuroblastomas start in the
adrenal glands. About 1 out of 3 begins in the sympathetic nerve
ganglia of the abdomen. The rest start in sympathetic ganglia of the
chest or neck or in the pelvis.
In rare cases, a neuroblastoma may have spread so widely by
the time it is found that doctors can't tell exactly where it started.
Neuroblastomas can behave strangely. Sometimes the cells die
without any cause and the tumor disappears. Tumor disappearance is much
more common in very young infants than in older children. Another
behavior that is unusual for childhood tumors is that the cells
sometimes mature spontaneously into normal ganglion cells and stop
dividing. This causes the tumor to become a ganglioneuroma (see below).
Other autonomic nervous system tumors
Not all childhood autonomic nervous system tumors are
malignant (cancerous). There is a benign tumor called ganglioneuroma
which is made up of of mature ganglion and nerve sheaths that do not
continue to grow.
Ganglioneuroblastoma
is a tumor that has both malignant and benign parts. It contains
neuroblasts (immature nerve cells) that can grow and spread abnormally,
as well as areas of more mature tissue that are similar to
ganglioneuroma.
Ganglioneuromas are usually removed by surgery and looked at
carefully under a microscope to be certain they do not have areas of
ganglioneuroblastoma. If the final diagnosis is ganglioneuroma, no
other treatment is needed. In contrast, ganglioneuroblastomas are
treated the same as neuroblastomas (see the section "How
is neuroblastoma treated?").
Last Medical Review: 10/22/2008 Last Revised: 10/22/2008
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