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  2. Pheochromocytoma - Wikipedia

    en.wikipedia.org/wiki/Pheochromocytoma

    Metastatic pheochromocytoma is best managed with a multidisciplinary team of oncologists, surgeons, radiologists, nuclear medicine physicians, and endocrinologists. There are several treatment options available to patients depending on the amount and location of disease:

  3. Multiple endocrine neoplasia type 2 - Wikipedia

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

    Before gene testing was available, the type and location of tumors determined which type of MEN2 a person had. Gene testing now allows a diagnosis before tumors or symptoms develop. [citation needed] Comparison of main types of multiple endocrine neoplasia. A table in the multiple endocrine neoplasia article compares the various MEN syndromes ...

  4. Multiple endocrine neoplasia type 2B - Wikipedia

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

    MEN2B should be entertained as a diagnosis whenever a person is found to have either medullary thyroid carcinoma or pheochromocytoma. Before DNA testing became available, measurement of serum calcitonin was the most important laboratory test for MEN2B. Calcitonin is produced by the "C" cells of the thyroid, which, because they are always ...

  5. WHO model list of essential in vitro diagnostics - Wikipedia

    en.wikipedia.org/wiki/WHO_Model_List_of...

    Where there is a health care facility with laboratories, tests are divided into either general tests or disease-specific tests for clinical laboratories, and disease-specific tests for blood screening laboratories. [5] For each group of tests, the EDL specifies the test's name, purpose, assay format and type of specimen. [6]

  6. Paraganglioma - Wikipedia

    en.wikipedia.org/wiki/Paraganglioma

    When the same type of tumor is found in the adrenal gland, they are referred to as a pheochromocytoma. They are rare tumors, with an overall estimated incidence of 1 in 300,000. [1] There is no test that determines benign from malignant tumors; long-term follow-up is therefore recommended for all individuals with paraganglioma. [2]

  7. Self-tests recommended for women ages 30 to 65 to ... - AOL

    www.aol.com/news/self-tests-recommended-women...

    The U.S. Preventive Services Task Force said the draft recommendations aim to avoid unnecessary follow-up tests and procedures. Self-tests recommended for women ages 30 to 65 to screen for ...

  8. Von Hippel–Lindau disease - Wikipedia

    en.wikipedia.org/wiki/Von_Hippel–Lindau_disease

    The detection of tumours specific to VHL disease is important in the disease's diagnosis. In individuals with a family history of VHL disease, one hemangioblastoma, pheochromocytoma or renal cell carcinoma may be sufficient to make a diagnosis. As all the tumours associated with VHL disease can be found sporadically, at least two tumours must ...

  9. Gallium scan - Wikipedia

    en.wikipedia.org/wiki/Gallium_scan

    Gallium scan showing panda (A) and lambda (B) patterns, considered specific for sarcoidosis in the absence of histological confirmation. In the past, the gallium scan was the gold standard for lymphoma staging, until it was replaced by positron emission tomography (PET) using 18 F-fluorodeoxyglucose (FDG).