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Recent News and Articles on the Keywords: pineal tumors + pineal + tumor  Related to the article below (Last Update: 8/5/2008)

Oh My! Three Fun Ways To Die
American Chronicle, CA - Jul 17, 2008
And the fluoride that we consume is said to collect in the pineal gland nestled deep in our brains. Rene Descartes referred to the pineal gland as The Seat ...
YOUR BIRTHDAY: Is it purely coincidence?
Colorado Daily, CO - Jul 9, 2008
Melatonin, a hormone secreted by the pineal gland in the brain in response to darkness, is suppressed by sunshine. Salib has speculated that having too much ...
Source: Google News

A multivariate analysis of prognostic factors in management of pineal tumor. -
CK Chao, ST Lee, FJ Lin, SG Tang, WM Leung - Int J Radiat Oncol Biol Phys, 1993 - ncbi.nlm.nih.gov
... tumor. METHODS AND MATERIALS: From February 1979 to June 1987, 25 patients
with primary pineal tumors were treated in our department. ...

Tryptophan Hydroxylation: Measurement in Pineal Gland, Brainstem, and Carcinoid Tumor -
W Lovenberg, E Jequier, A Sjoerdsma - Science, 1967 - sciencemag.org
... in several mammalian tissues and assay of enzyme activity in certain serotonin-rich
tissues including pineal gland, brainstem, and carcinoid tumor. ...

Melatonin replacement corrects sleep disturbances in a child with pineal tumor -
A Etzioni - Neurology, 1996 - AAN Enterprises
... Academy of Neurology. ARTICLES. Melatonin replacement corrects sleep disturbances
in a child with pineal tumor. A Etzioni, R Luboshitzky ...

Surgical management of pineal region tumors -
JN Bruce, BM Stein - Acta Neurochirurgica, 1995 - Springer
... One-third of pineal tumors were benign for which surgery alone was usually curative. ...
Neuro- surg Quart 3:103-119 3. Bruce JN, Stein BM (1990) Pineal tumors. ...

[CITATION] Operative experience in cases of pineal tumor
WE Dandy - Arch Surg, 1936

Pineal region tumors in children. -
MS Edwards, RJ Hudgins, CB Wilson, VA Levin, WM … - J Neurosurg, 1988 - ncbi.nlm.nih.gov
J Neurosurg. 1988 May;68(5):689-97. Pineal region tumors in children. Edwards
MS, Hudgins RJ, Wilson CB, Levin VA, Wara WM. Department ...

Malignant pineal region tumors. A clinico-pathological study.
EA Neuwelt, M Glasberg, E Frenkel, WK Clark - J Neurosurg, 1979 - ncbi.nlm.nih.gov
... Eight patients with primary malignant pineal tumors have been seen at this institution
over the past 6 years; six of them underwent definitive surgical ...

MR imaging of pineal tumors.
RD Tien, AJ Barkovich, MS Edwards - AJR Am J Roentgenol, 1990 - ncbi.nlm.nih.gov
AJR Am J Roentgenol. 1990 Jul;155(1):143-51. Click here to read MR imaging
of pineal tumors. Tien RD, Barkovich AJ, Edwards MS. ...

Pineal tumors: experience with 48 cases over 10 years -
BK Cho, KC Wang, DH Nam, DG Kim, HW Jung, HJ Kim, … - Child's Nervous System, 1998 - Springer
... OPERATIVE TECHNIQUES Pineal tumors: experience with 48 cases over 10 years ... proce-
dure. Results Incidence of pineal tumors In this series ...

Diagnosis and management of pineal tumors.
R Jooma, BE Kendall - J Neurosurg, 1983 - ncbi.nlm.nih.gov
Diagnosis and management of pineal tumors. Jooma R, Kendall BE. ... This paper reports
a study of 35 patients with pineal tumors including two ectopic germinomas. ...

Source: Google Scholar
 

Pineal Tumors

Tumors in the region of the pineal gland account for about one percent of brain tumors. Many different types of tumors with completely different characteristics occur in this region, but the most common type is called a germinoma.

Symptoms

When pineal tumors occur in childhood, they can produce an early puberty, especially in boys. This type of tumor causes pressure in the channel that connects two cavities of the brain where fluid flows around the brain and spinal cord. The tumor can cause pressure inside the brain (leading to hydrocephalus), swelling inside the eye and vomiting. It can also cause paralysis of the upward gaze, sagging or drooping of the upper eyelid and a loss of reflex reactions in the eye.

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Causes and Risk Factors

Pineal tumors can occur at any age, but they are most common in childhood.

Diagnosis

A neurologic evaluation should be done if a patient has slowly increasing signs of mental dysfunction, new seizures, persistent headaches or evidence that there is pressure inside the skull (such as vomiting or swelling or protrusion of the blind spot at the back of the eye). A neurologist (a doctor who has received special additional training in the diagnosis and treatment of disorders of the brain, spinal cord and nerves) will perform a complete examination.

He or she may also request that a magnetic resonance imaging (MRI) scan or a computed tomography (CT or CAT) scan be done, as well as chest X-rays, to determine if the tumor has spread from another part of the body. An MRI usually finds low-grade astrocytomas earlier than CT. Cerebral angiography is rarely used to diagnose a brain tumor, but it may be done before surgery.

Depending on the patient's symptoms, specialized tests may be done, including tests of the field of vision, the sharpness of vision and hearing. If the results of other tests are not conclusive, an examination of the fluid that surrounds the brain and spinal cord may be done, although it is usually unnecessary. It is essential for diagnosing chronic or subacute meningitis or for identifying benign hypertension inside the skull.

Treatment

Treatment of a brain tumor depends on the nature of the tumor, how rapidly it is growing, what symptoms it is causing and where it is located. Several treatment approaches may be used. Surgery is usually done to make a diagnosis and to improve symptoms. This may be enough to cure benign tumors.

Radiation therapy is required to treat gliomas. Radiation therapy may also be beneficial in the short-term for tumors that have spread from other parts of the body. Chemotherapy also benefits some patients with such tumors.

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Pituitary Adenomas

The pituitary gland is a small oval gland at the base of the brain. It controls most of our hormones. These control thyroid activity, the monthly cycle in women, sex drive, growth in children, adrenal gland activity, urine output, the start childbirth and milk-production after pregnancy.

Doctors describe these tumors in several ways. One is as:

  • Secreting, which release hormones. These can trigger symptoms such as impotence, stopping of a woman's monthly periods, galactorrhea, abnormal body growth, Cushing's syndrome or hyperthyroidism.
  • Non-secreting, which are usually larger when found and treated with surgery and radiation therapy.

Another is by size:

  • Microadenomas, which are smaller than one centimeter
  • Macroadenomas, which are larger than one centimeter. These can be quite large if not found until they affect nearby brain tissues. The optic nerves are particularly vulnerable. Early on, the vision at the edges of the field of sight can be affected. Pituitary tumors can spread into the area of the head that contains the carotid artery and cranial nerves. When this occurs, the tumors may be particularly difficult to completely remove.

Symptoms

Symptoms vary based on the tumor's size, where it is and whether it secretes or not. They may include:

  • Overproduction of hormones. Functional tumors, which secrete hormones, can produce too much hormones. Almost 20% secrete prolactin, a hormone that causes milk production in women. Very high levels can cause milk production in men and women who are not pregnant. Menstrual irregularities may also occur.
  • Underproduction of hormones. Some 75% of pituitary tumors don't produce hormones. These can grow and damage normal gland tissue. This cuts hormone production. Often the first hormones affected are those that relate to sex. This can cause irregularity or loss of menstruation in women and sterility with loss of sex drive in men and women.
  • Growth disorders. These cause excessive growth (gigantism) in children. In adults, they cause acromegaly, or abnormal growth of the face bones, enlarged hands and feet, excessive sweating and heart disease.
  • Disturbances in vision will occur if the tumor presses on the optic nerves.

Diagnosis

A magnetic resonance imaging (MRI) scan is the most sensitive test for pituitary tumors. It can rapidly show even small tumors. Sometimes computed tomography (CT) scanning is used. However, this may not detect small tumors.

Complete hormone testing is also important. An endocrinologist may need to be consulted. A complete neurological evaluation, including a visual field exam, is also needed to see if there is any visual loss.

Treatment

Treatment is set by the size of the tumor and the patient's symptoms and hormone status. Reducing pressure on nearby structures (generally the optic nerves) and restoring normal hormone production is important.

Treatment may include:

  • Observation and monitoring with MRI scans and visual field studies, if the patient's vision is not threatened and hormone production is normal
  • Surgery
  • Stereotactic radiosurgery
  • Radiation therapy
  • Drugs

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