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  2. Nelson's syndrome - Wikipedia

    en.wikipedia.org/wiki/Nelson's_syndrome

    Nelson's syndrome is a disorder that occurs in about one in four patients who have had both adrenal glands removed to treat Cushing's disease. In patients with pre-existing adrenocorticotropic hormone ()-secreting pituitary adenomas, loss of adrenal feedback following bilateral adrenalectomy can trigger the rapid growth of the tumor, leading to visual symptoms (e.g. bitemporal hemianopsia) and ...

  3. Pituitary adenoma - Wikipedia

    en.wikipedia.org/wiki/Pituitary_adenoma

    Pituitary adenomas are tumors that occur in the pituitary gland. Most pituitary tumors are benign, approximately 35% are invasive and just 0.1% to 0.2% are carcinomas. [1] Pituitary adenomas represent from 10% to 25% of all intracranial neoplasms and the estimated prevalence rate in the general population is approximately 17%.

  4. Sheehan's syndrome - Wikipedia

    en.wikipedia.org/wiki/Sheehan's_syndrome

    Sheehan's syndrome, also known as postpartum pituitary gland necrosis, occurs when the pituitary gland is damaged due to significant blood loss and hypovolemic shock (ischemic necrosis) usually during or after childbirth leading to decreased functioning of the pituitary gland ( hypopituitarism ). [1] The pituitary gland is an endocrine organ ...

  5. Craniopharyngioma - Wikipedia

    en.wikipedia.org/wiki/Craniopharyngioma

    A craniopharyngioma is a rare type of brain tumor derived from pituitary gland embryonic tissue 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]

  6. Pituitary apoplexy - Wikipedia

    en.wikipedia.org/wiki/Pituitary_apoplexy

    The initial symptoms of pituitary apoplexy are related to the increased pressure in and around the pituitary gland. The most common symptom, in over 95% of cases, is a sudden-onset headache located behind the eyes or around the temples. It is often associated with nausea and vomiting. [1] [2] [3] Occasionally, the presence of blood leads to ...

  7. Horror fusionis - Wikipedia

    en.wikipedia.org/wiki/Horror_fusionis

    Horror fusionis is a rare condition and normally appears only in patients who have been treated by means of surgery or other interventions. Attempts to achieve stereoscopic vision, in particular anti-suppression therapy and other orthoptic exercises, may lead to double vision as undesired side effect, in particular also to horror fusionis.

  8. Empty sella syndrome - Wikipedia

    en.wikipedia.org/wiki/Empty_sella_syndrome

    Pituitary gland. The cause of this condition is divided into primary and secondary, as follows: The cause of this condition in terms of secondary empty sella syndrome happens when a tumor or surgery damages the gland, this is an acquired manner of the condition. patients with idiopathic intracranial hypertension will have empty sella on MRI

  9. Endoscopic endonasal surgery - Wikipedia

    en.wikipedia.org/wiki/Endoscopic_endonasal_surgery

    An endocrinologist is only involved in preparation for an endoscopic endonasal surgery, if the tumor is located on the pituitary gland. The tumor is first treated pharmacologically in two ways: controlling the levels of hormones that the pituitary gland secretes and reducing the size of the tumor. If this approach does not work, the patient is ...

  10. Esotropia - Wikipedia

    en.wikipedia.org/wiki/Esotropia

    Esotropia is a form of strabismus in which one or both eyes turn inward. The condition can be constantly present, or occur intermittently, and can give the affected individual a "cross-eyed" appearance. [1] It is the opposite of exotropia and usually involves more severe axis deviation than esophoria. Esotropia is sometimes erroneously called ...

  11. Multiple endocrine neoplasia type 1 - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine...

    About 3% of tumors secrete ACTH, producing Cushing's disease. Most of the remainder are nonfunctional. Local tumor expansion may cause visual disturbance, headache, and hypopituitarism. Pituitary tumors in MEN 1 patients appear to be larger and behave more aggressively than sporadic pituitary tumors. Other manifestations