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  2. Multiple endocrine neoplasia type 1 - Wikipedia

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

    Pituitary tumor in MEN1 can be large and cause signs by compressing adjacent tissues. Pancreatic tumors associated with MEN-1 usually form in the beta cells of the islets of Langerhans, causing over-secretion of insulin, resulting in low blood glucose levels (hypoglycemia). However, many other tumors of the pancreatic Islets of Langerhans can ...

  3. 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 ...

  4. Multiple endocrine neoplasia - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine_neoplasia

    Multiple endocrine neoplasia (abbreviated MEN) is a condition which encompasses several distinct syndromes featuring tumors of endocrine glands, each with its own characteristic pattern. In some cases, the tumors are malignant, in others, benign. Benign or malignant tumors of nonendocrine tissues occur as components of some of these tumor ...

  5. What Is Low Testosterone & What Causes It? - AOL

    www.aol.com/low-testosterone-causes-125700734.html

    These signs and symptoms may vary in severity and affect the quality of your life. Some of the most common signs and symptoms of low testosterone in men include: Reduced drive. ED. Testicular ...

  6. 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.

  7. 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 ).

  8. Macroorchidism - Wikipedia

    en.wikipedia.org/wiki/Macroorchidism

    Treatment of macroorchidism depends on pathogenesis. Surgical removal of the tumor is the most important and advised option for treating macroorchidism caused by non-functioning pituitary macroadenoma. [12] A non-functioning pituitary adenoma is a kind of benign tumor that does not secrete active hormones, and is from the pituitary gland. [13]

  9. Hyperprolactinaemia - Wikipedia

    en.wikipedia.org/wiki/Hyperprolactinaemia

    Men often present late in the course of hyperprolactinemia, typically symptoms are related to the expansion of their pituitary tumor, such as headaches, visual defects, and external opthalmoplegia, or symptoms from secondary adrenal or thyroid failure. [8]