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  2. Pituitary adenoma - Wikipedia

    en.wikipedia.org/wiki/Pituitary_adenoma

    Surgery is a common treatment for pituitary tumors. The normal approach is trans-sphenoidal adenectomy, which usually can remove the tumor without affecting the brain or optic nerves. [70] Radiation is also used to treat pituitary adenomas. Examples include external beam or proton beam radiation therapy or stereotactic radiosurgery.

  3. What does growth hormone therapy treat? What an ... - AOL

    www.aol.com/does-growth-hormone-therapy-treat...

    Growth hormone treatment is a safe and effective therapy that’s often used to ... Children born small for gestational age without catch-up growth ... Tumors in the pituitary gland. Brain surgery.

  4. Pegvisomant - Wikipedia

    en.wikipedia.org/wiki/Pegvisomant

    Pegvisomant, sold under the brand name Somavert, is a growth hormone receptor antagonist used in the treatment of acromegaly. [1] [2] [3] It is primarily used if the pituitary gland tumor causing the acromegaly cannot be controlled with surgery or radiation, and the use of somatostatin analogues is unsuccessful, but is also effective as a monotherapy. [4]

  5. Pituitary apoplexy - Wikipedia

    en.wikipedia.org/wiki/Pituitary_apoplexy

    The pituitary gland consists of two parts, the anterior (front) and posterior (back) pituitary. Both parts release hormones that control numerous other organs. In pituitary apoplexy, the main initial problem is a lack of secretion of adrenocorticotropic hormone (ACTH, corticotropin), which stimulates the secretion of cortisol by the adrenal ...

  6. Prolactinoma - Wikipedia

    en.wikipedia.org/wiki/Prolactinoma

    Surgery should be considered if medical therapy cannot be tolerated or if it fails to reduce prolactin levels, restore normal reproduction and pituitary function, and reduce tumor size. If medical therapy is only partially successful, this therapy should continue, possibly combined with surgery or radiation treatment. [11]

  7. Craniopharyngioma - Wikipedia

    en.wikipedia.org/wiki/Craniopharyngioma

    A craniopharyngioma is a rare type of brain tumor derived from pituitary gland embryonic tissue [1] that occurs most commonly in children, but also affects adults. It may present at any age, even in the prenatal and neonatal periods, but peak incidence rates are childhood-onset at 5–14 years and adult-onset at 50–74 years. [2]

  8. Endoscopic endonasal surgery - Wikipedia

    en.wikipedia.org/wiki/Endoscopic_endonasal_surgery

    The tumor normally results in acral enlargement, arthropathy, hyperhidrosis, changes in facial features, soft tissue swelling, headaches, visual changes, or hypopituitarism. Since pharmacological therapy has had little effect on these tumors, a trans-sphenoidal surgery to remove part of the pituitary gland is the first treatment option. [5]

  9. Hypopituitarism - Wikipedia

    en.wikipedia.org/wiki/Hypopituitarism

    Pituitary tumors require treatment when they are causing specific symptoms, such as headaches, visual field defects or excessive hormone secretion. Transsphenoidal surgery (removal of the tumor by an operation through the nose and the sphenoidal sinuses ) may, apart from addressing symptoms related to the tumor, also improve pituitary function ...

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