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  2. Pituitary adenoma - Wikipedia

    en.wikipedia.org/wiki/Pituitary_adenoma

    Familial isolated pituitary adenoma (FIPA) is a term that is used to identify a condition that displays an autosomal dominant inheritance and is characterised by the presence of two or more related patients affected by adenomas of the pituitary gland only, with no other associated symptoms that occur in multiple endocrine neoplasia type 1 (MEN ...

  3. Multiple endocrine neoplasia type 1 - Wikipedia

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

    If the tumors become cancerous, some cases can be life-threatening. The disorder affects 1 in 30,000 people. Although many different types of hormone-producing tumors are associated with multiple endocrine neoplasia, tumors of the parathyroid gland, pituitary gland, and pancreas are most frequent in multiple endocrine neoplasia type 1.

  4. Prolactinoma - Wikipedia

    en.wikipedia.org/wiki/Prolactinoma

    A prolactinoma is a tumor of the pituitary gland that produces the hormone prolactin.It is the most common type of functioning pituitary tumor. [1] Symptoms of prolactinoma are due to abnormally high levels of prolactin in the blood (hyperprolactinemia), or due to pressure of the tumor on surrounding brain tissue and/or the optic nerves.

  5. Pituitary apoplexy - Wikipedia

    en.wikipedia.org/wiki/Pituitary_apoplexy

    Many pituitary tumors (25%) are found to have areas of hemorrhagic infarction on MRI scans, but apoplexy is not said to exist unless it is accompanied by symptoms. [ 1 ] [ 4 ] In some instances, lumbar puncture may be required if there is a suspicion that the symptoms might be caused by other problems ( meningitis or subarachnoid hemorrhage ).

  6. Cushing's disease - Wikipedia

    en.wikipedia.org/wiki/Cushing's_disease

    The symptoms of Cushing's disease are similar to those seen in other causes of Cushing's syndrome. [5] Patients with Cushing's disease usually present with one or more signs and symptoms secondary to the presence of excess cortisol or ACTH. [6] Although uncommon, some patients with Cushing's disease have large pituitary tumors (macroadenomas).

  7. Hyperpituitarism - Wikipedia

    en.wikipedia.org/wiki/Hyperpituitarism

    Hyperpituitarism is a condition due to the primary hypersecretion of pituitary hormones; [3] [medical citation needed] it typically results from a pituitary adenoma.In children with hyperpituitarism, disruption of growth regulation is rare, either because of hormone hypersecretion or because of manifestations caused by local compression of the adenoma.

  8. 29-Year-Old in ‘Catatonic State’ After Rare Disorder Causes ...

    www.aol.com/lifestyle/29-old-catatonic-state...

    As the Cleveland Clinic explains, the disorder presents “with a range of neuropsychiatric symptoms” like Tarver experienced, and is commonly caused by a tumor.. However, the GoFundMe says ...

  9. 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. [1] 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 ...

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