Craniopharyngioma: Symptoms, Causes, Diagnosis, and Treatment
Summary
TLDRDr. Aaron Cohen Gadol discusses craniopharyngiomas, a rare, benign brain tumor near the pituitary gland. He outlines symptoms like headaches and vision problems, common in children and older adults. Treatment options include observation, radiation, and surgery, with the latter often requiring a balance between removal and preserving gland function. Despite potential complications and recurrence, survival rates are high, emphasizing the importance of an experienced surgeon for optimal outcomes.
Takeaways
- đ§ Craniopharyngiomas are benign, slow-growing brain tumors typically occurring near the pituitary gland and hypothalamus.
- đ„ These tumors can compress surrounding structures like the optic nerve, affecting vision, but they are not cancerous.
- đ Incidence is rare, affecting less than two people per one million per year, with two age peaks: children aged 5-14 and adults aged 50-70.
- đŹ Key terminologies include 'pituitary gland', a hormone-producing gland, and 'hormone', which controls cell or tissue actions.
- đ€ Typical symptoms include headaches, vomiting, visual problems, and less commonly, confusion, excessive thirst, fatigue, and cognitive issues.
- đ Diagnostic tests include CT scans for calcifications and MRI for tumor differentiation from surrounding tissues.
- đ ïž Treatment options encompass observation, radiation, and surgical resection, often requiring a combination for effective management.
- âïž Surgical resection is primary but complex due to the tumor's adhesive nature; complete removal may require hormone replacement.
- â ïž Surgical complications can include vision deterioration, hormonal imbalances, excessive thirst or urination, and optic neuropathy.
- đšââïž The experience of the surgeon is critical for a favorable outcome, with maximal safe tumor removal as the goal.
- đ Recurrence is possible in nearly a third of cases but can be managed with additional therapies, including radiation.
- đŻ Prognosis is favorable, with 90% of adults and children alive and functional at 10 years post-treatment.
Q & A
What is a craniopharyngioma?
-A craniopharyngioma is a benign, slow-growing brain tumor that typically occurs near the pituitary gland and the hypothalamus, often compressing surrounding structures like the optic nerve.
Is a craniopharyngioma a type of cancer?
-No, a craniopharyngioma is not a cancer. It is a benign tumor, meaning it is not cancerous and does not spread to other parts of the body.
How common are craniopharyngiomas?
-Craniopharyngiomas are rare, affecting less than two people per one million people per year and accounting for about 1-3% of all brain tumors.
What are the two age peaks for the occurrence of craniopharyngiomas?
-The two age peaks for the occurrence of craniopharyngiomas are in children between the ages of 5 to 14 and older adults between the ages of 50 to 70.
What is the role of the pituitary gland in relation to craniopharyngiomas?
-The pituitary gland is closely associated with craniopharyngiomas. It is a small, bean-shaped gland at the base of the skull that produces hormones critical for body function, such as growth hormones.
What are the typical symptoms of a craniopharyngioma?
-The typical symptoms of a craniopharyngioma include headache, vomiting, and visual problems. Less common symptoms can include confusion, extreme thirst or urination, feeling tired, loss of appetite, weight changes, and problems with thinking or learning.
What diagnostic tests are used to identify craniopharyngiomas?
-Diagnostic tests for craniopharyngiomas include CT scans, which can identify calcifications within the gland, and MRI, which can differentiate the tumors from surrounding soft tissues and identify cysts filled with fluid.
What are the treatment options for craniopharyngiomas?
-Treatment options for craniopharyngiomas include observation, radiation, and surgical resection. Surgical resection is the primary mode of treatment, but most patients may require a combination of these options.
What is radiosurgery and how is it used in treating craniopharyngiomas?
-Radiosurgery is a treatment that uses concentrated beams of radiation aimed at the tumor while protecting the surrounding vital structures. It is particularly effective for recurrent tumors or tumors that cannot be easily or safely removed via surgery.
What are some potential complications of surgery for craniopharyngiomas?
-Potential complications of surgery for craniopharyngiomas include vision deterioration, hormonal abnormalities due to injury to the pituitary gland, excessive thirst or urination, leakage of brain fluid through the nose, hyperphagia, and radiation-induced optic neuropathy.
What is the most common surgical approach for removing craniopharyngiomas?
-The most common surgical approach for removing craniopharyngiomas is through the nose using a transvenor operation, which provides the most effective and least invasive pathway to remove the tumor.
What is the long-term outlook for patients with craniopharyngiomas?
-The long-term outlook for patients with craniopharyngiomas is favorable, with a survival rate of 90% for both adults and children at 10 years. However, nearly a third of the tumors can recur and may require additional treatment.
Outlines
đ§ Understanding Craniopharyngiomas: A Neurosurgeon's Perspective
Dr. Aaron Cohen Gadol, a neurosurgeon with extensive experience in managing chronic craniopharyngiomas, introduces the topic and provides an overview of these benign, slow-growing brain tumors. He clarifies that they are not cancerous and typically occur near the pituitary gland and hypothalamus, potentially affecting vision. The tumors' sticky nature makes complete resection challenging, leading to recurrence. They are rare, affecting less than two people per million annually, with symptoms more common in children aged 5-14 and adults aged 50-70. Key terminologies include the pituitary gland, a hormone-producing gland, and hormones, like growth hormones, which are critical for body functions.
đ ïž Treatment and Management of Craniopharyngiomas
The script continues with an in-depth discussion on the diagnosis and treatment options for craniopharyngiomas. Initial tests include CT scans to identify calcifications and MRIs to differentiate the tumor from surrounding tissues. Treatment options range from observation for small, asymptomatic tumors to surgical resection, which is the primary mode of treatment but may require a combination of approaches due to the tumor's complex nature. Surgical resection aims for maximal tumor removal, but complete removal may necessitate sacrificing the pituitary gland function, leading to lifelong hormone replacement. Complications of surgery can include vision deterioration, hormonal abnormalities, excessive thirst or urination, leakage of brain fluid, hyperphagia, and radiation-induced optic neuropathy. The most common surgical approach is the transvenor operation through the nose. The patient's journey involves lifelong management, with nearly a third of tumors recurring but being treatable with other therapies. The survival rate is high, with 90% of adults and children alive and functional after 10 years. Dr. Cohen Gadol emphasizes the importance of the surgeon's experience for a favorable outcome and offers his expertise for second opinions.
Mindmap
Keywords
đĄNeurosurgeon
đĄChronic Pharyngeal Tumor
đĄPituitary Gland
đĄHormone
đĄSymptoms
đĄCT Scan
đĄMRI
đĄRadiosurgery
đĄFractionated Radiotherapy
đĄSurgical Resection
đĄComplications
Highlights
Introduction to the topic by neurosurgeon Aaron Cohen-Gadol, focusing on chronic craniopharyngiomas.
Definition of craniopharyngiomas as benign and slow-growing brain tumors, typically near the pituitary gland and hypothalamus.
Craniopharyngiomas can compress surrounding structures such as the optic nerve, affecting vision.
Despite being benign, the tumors are sticky to normal structures, making complete resection challenging.
Craniopharyngiomas are rare, affecting less than two people per million annually and accounting for about 1-3% of all brain tumors.
The tumors are most commonly seen in children aged 5-14 and older adults aged 50-70.
Explanation of key terminologies: the pituitary gland and hormones, particularly growth hormones.
Typical symptoms of craniopharyngiomas include headaches, vomiting, and visual problems, with less common symptoms being confusion, extreme thirst or urination, and slow growth.
Diagnostic tests include CT scans for detecting calcifications and MRIs for detailed imaging of the tumor and surrounding tissues.
Treatment options: observation, radiation, and surgical resection, with surgery being the primary mode of treatment.
Observation is recommended for small, asymptomatic tumors, with regular MRI follow-ups.
Radiosurgery and fractionated radiotherapy are alternatives for recurrent or non-removable tumors, with details on each method's process and effectiveness.
Surgical resection aims to remove as much of the tumor as safely possible, with complete removal sometimes requiring hormone replacement for life.
Potential complications from surgery include vision deterioration, hormonal abnormalities, and excessive thirst or urination.
The most common surgical approach is the transsphenoidal operation, providing an effective and minimally invasive pathway for tumor removal.
Craniopharyngiomas are chronic conditions requiring lifelong treatment, with up to a third of tumors potentially recurring.
Despite the challenges, survival rates are favorable, with 90% of patients being alive and functional at 10 years.
Emphasis on the importance of the surgeon's experience for a favorable outcome and safe maximal tumor removal.
Encouragement for patients to seek a second opinion consultation if needed.
Transcripts
[Music]
hello ladies and gentlemen my name is
aaron cohen gadol i'm a neurosurgeon
i've been involved in the management of
patients suffering from chronic friend
jomos for many years and today i'd like
to talk to you about the information
that is important for the journey of the
patients after they have been diagnosed
with this tumor type
so what is a chronic pharyngeal it's a
brain tumor that
is benign and slow growing that's very
important this tumor is not a cancer
and it occurs typically near the
pituitary gland and the hypothalamus in
other words at the level of the skull
base it can compress the surrounding
structures such as the optic nerve in
other words the vision nerve that takes
information from the eyes to the brain
and effect
visualization
of things every day
also because they're sticky to the
normal structures complex resection
unfortunately is not possible and
therefore these tumors tend to occur and
that tends to be the most challenging
detail under management
fortunately these tumors are rare they
affect less than two people per
one million people per year they account
for about one to two one to three
percent of all brain tumors
and the symptoms are more commonly seen
in children between the age of 5 to 14
and older adults in the age of 50 to 70.
so there are two peaks of age for this
tumor type there is a couple of
terminologies that are very important
for patients who have been diagnosed
with a chronic pharyngeal the first
terminology is a pituitary gland it is a
gland that is very much
involved with these tumors and closely
associated the pituitary gland is a
small bean shaped gland at the level of
the skull base
that produces hormones that are very
critical for body function such as
growth hormones
and the second terminology is what is a
hormone it's a chemical substance such a
growth such as a growth hormone that
helps controls actions of cells or
tissues in the body
and more specifically for the growth
hormone would be controlling the growth
so what are the typical symptoms related
to chronic pharyngeals number one is
headache vomiting or visual problems
these are the top three problems that
can be associated with a
cranipharyngeoma
there are other less common symptoms
such as confusion extreme thirst or
urination feeling tired loss of appetite
weight changes problems with thinking or
learning and slow growth
or
other related
problems
what are the tests that we typically use
the first test is using a ct scan or a
computer tomography where we can see the
calcifications within the gland and
obviously very importantly an mri
magnetic resonance imaging where the
tumors are easily differentiated from
the surrounding soft tissues
and their character in terms of having
cysts filled with fluid are found
but typically in this area
presence of calcification of ct scan and
cysts in the tumor
signifies the presence of a
craniopharyngioma
relative to a typical pituitary tumor
what are the options for treatment
observation radiation and
surgical resection surgical resection is
the primary mode of treatment
however at the end
most
of the patient require
three of these options in some form
uh to treat the tumor most effectively
so when we start
with observation this is
for tumors that are relatively small
they're asymptomatic
and these tumors can be observed and
obviously every six months or a year mri
is performed to make sure the tumor is
not growing
also radiosurgery may be an option for
these tumors that is most effective
for recurrent tumors or tumors that
cannot be removed
easily via surgery
or safely
what is radiosurgery is concentrated
beams of radiation that are aimed
at the tumor while preserving and
protecting the surrounding vital
structures it takes this takes about 30
to 50 minutes and the patients go home
same day
also there is another form of
radiotherapy called fractionated
radiotherapy this is smaller dose of
radiation that are aimed at the tumor
over several visits up to
you know a month of treatment
and it takes up to 18 months
or more for the radiation to take effect
and stop the growth of the tumor
when we talk about surgery
the surgeon tries to remove as much of
the tumor wholly or partially
the more the tumor is removed the better
it is obviously it requires an
experienced surgeon to be able to remove
as much of the tumor as safely as
possible
partial removal again is for those
situations where the tumor is very stuck
to the vessels or the pituitary gland
itself
complete removal is possible but may
require sacrificing the pituitary gland
function and hormone replacement for the
rest of life
what are the complications related to
surgery it could be vision deterioration
hormonal abnormalities due to
injury to the pituitary gland because
this tumor typically arises and is very
much associated with the stock of the
pituitary gland which
controls the functions of the pituitary
gland
excessive thirst or urination can be
long-term complications related to the
failure of the pituitary gland
leakage of brain fluid through the nose
and strong sensation of hunger
hyperphagia in other words especially
among the children who undergo this
procedure and also radiation induced
optic neuropathy in other words
injury to the optic nerve because of
radiation can be another complication
related to this tumor
the most common approach for removal of
the tumor is through the nose through a
transvenor operation
because this provides the most effective
pathway and least invasive to be able to
remove this tumor
so
what's important to know about chronic
pharyngeal pharyngeals that are cru they
are chronic conditions in other words
the patient require some sort of
treatment for the rest of their life
in terms of radiation treatment or
hormonal therapy to be able to manage
their treatment very effectively
unfortunately nearly up to a third of
tumor can recur but can be treated with
other modes of therapy including
radiation
survival is very favorable with 90 of
the adults and children alive and
functional at 10 years so overall as a
patient i would like you to know
that these tumors are not cancerous very
effective therapies exist
experience of the surgeon is critical
for favorable outcome a maximal tumor
removal
safely it has been an honor for me for
the past 20 years to be involved with
the care of many of patients suffering
from this tumor type and i'll be more
than happy to provide you with a second
consult second opinion consultation if
needed thank you
[Music]
Voir Plus de Vidéos Connexes
Chondrosarcoma: Symptoms, Causes, Diagnosis, and Treatment - Aaron Cohen-Gadol, M.D.
Colorectal carcinoma - causes, symptoms, diagnosis, treatment, pathology
What is Cancer? (HealthSketch)
Cerebral Aneurysm
Cancer: Pathophysiology, Risk Factors, Signs/Symptoms and more - Medical Surgical | @LevelUpRN
Intussusception - causes, symptoms, diagnosis, treatment, pathology
5.0 / 5 (0 votes)