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  2. Paraganglioma - Wikipedia

    en.wikipedia.org/wiki/Paraganglioma

    Carotid paraganglioma (carotid body tumor): Is the most common of the head and neck paragangliomas. It usually presents as a painless neck mass, but larger tumors may cause cranial nerve palsies, usually of the vagus nerve and hypoglossal nerve .

  3. Carotid body - Wikipedia

    en.wikipedia.org/wiki/Carotid_body

    The carotid body is situated on the posterior aspect of the bifurcation of the common carotid artery. [3] The carotid body is made up of two types of cells, called glomus cells: glomus type I cells are peripheral chemoreceptors, and glomus type II cells are sustentacular supportive cells. Glomus type I cells are derived from the neural crest. [4]

  4. Paraganglion - Wikipedia

    en.wikipedia.org/wiki/Paraganglion

    Tumors of the paraganglionic tissues are known as paragangliomas, though this term tends to imply the nonchromaffin type, and can occur at a number of sites throughout the body. Chromaffin paragangliomas are issued from chromaffin cells, and are known as pheochromocytomas .

  5. Woman, 34, says doctors ‘brushed off’ her symptoms. She had ...

    www.aol.com/woman-34-says-doctors-brushed...

    About six weeks after her symptoms began, she insisted on an ultrasound and was eventually diagnosed with Stage 3 borderline ovarian tumors, a type of pre-cancerous mass.

  6. Glomus tumor - Wikipedia

    en.wikipedia.org/wiki/Glomus_tumor

    A glomus tumor (also known as a "solitary glomus tumor" [1]) is a rare neoplasm arising from the glomus body and mainly found under the nail, on the fingertip or in the foot. [2]: 670 They account for less than 2% of all soft tissue tumors. [3] The majority of glomus tumors are benign, but they can also show malignant features. [4]

  7. Pacak–Zhuang syndrome - Wikipedia

    en.wikipedia.org/wiki/Pacak–Zhuang_syndrome

    The most common therapies for secondary polycythemia are phlebotomies [9] and, for paraganglioma and/or somatostatinoma in this cohort of patients, surgery accompanied by antihypertensive medication. [1] HIF-2α inhibitor belzutifan led to substantial improvement of symptoms in a patient with Pacak–Zhuang syndrome. [10]

  8. Pheochromocytoma - Wikipedia

    en.wikipedia.org/wiki/Pheochromocytoma

    Pheochromocytoma is a rare tumor of the adrenal medulla composed of chromaffin cells and is part of the paraganglioma (PGL) family of tumors, being defined as an intra-adrenal PGL .

  9. Organ of Zuckerkandl - Wikipedia

    en.wikipedia.org/wiki/Organ_of_Zuckerkandl

    It can be the source of paraganglioma. [8]The organ of Zuckerkandl is of pathological significance in the adult as a common extra-adrenal site of pheochromocytoma though the most common extra-adrenal site is in the superior para-aortic region between the diaphragm and lower renal poles.