Results 301 to 310 of about 51,236 (315)
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Phaeochromocytoma and paraganglioma
Baillière's Clinical Endocrinology and Metabolism, 1993Use of current analytical techniques should lead to the successful diagnosis of most catecholamine-secreting tumours, and the experience and confidence which has evolved with the use of HPLC-ECD for plasma and urinary catecholamine estimation, as well as their greater diagnostic sensitivity and specificity, should soon render the older urinary assays ...
Vivian Fonseca +1 more
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Journal of Clinical Neuroscience, 2009
Mesenteric paraganglioma is a solitary primary paraganglioma that occurs in the mesentery. It is a rare and unusual tumor, especially in non-typical sites such as the inferior mesenteric artery. We incidentally diagnosed a pelvic mass in a 22-year-old woman, who had not experienced vomiting, headache or hypertension.
Zhilan Peng, Hui Liu, Na Guo
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Mesenteric paraganglioma is a solitary primary paraganglioma that occurs in the mesentery. It is a rare and unusual tumor, especially in non-typical sites such as the inferior mesenteric artery. We incidentally diagnosed a pelvic mass in a 22-year-old woman, who had not experienced vomiting, headache or hypertension.
Zhilan Peng, Hui Liu, Na Guo
openaire +3 more sources
Paraganglioma of the Gallbladder
Archives of Surgery, 1973To the Editor .—In the discussion of their well-documented case of paraganglioma of the gallbladder ( Arch Surg 105:637-639, 1972) Miller and co-authors stated that nonneoplastic paraganglionic tissue had not as yet been described in the gallbladder. In the Laboratory of Surgical Pathology at the College of Physicians and Surgeons, we have observed ...
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Pheochromocytoma and Paraganglioma
Seminars in Pediatric Surgery, 2020James K. Moon, Peter Mattei
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Pheochromocytoma and paraganglioma—an update on diagnosis, evaluation, and management
Pediatric nephrology (Berlin, West), 2019Amrish Jain, Rossana Baracco, G. Kapur
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