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Clinical and Experimental Pheochromocytoma

Clinical and Experimental Pheochromocytoma The new edition of Clinical and Experimental Pheochromocytoma by Drs Manger and Gifford is a unique compendium and textbook on this topic. The first edition was written entirely by the principal authors, but a number of other investigators have contributed to the second edition. All are experts in their fields and deserve gratitude and respect for sharing their knowledge with the reader. In 1886 Frankel first described pheochromocytomas that were found at autopsy in both adrenal glands of an 18-year-old girl. In 1922, L'Abbé and his colleagues first made the fascinating observation that paroxysms of high blood pressure occurred in a young woman who was found at autopsy to have an adrenal tumor. Volhard had previously described the clinical syndrome. A pheochromocytoma was successfully removed by Roux the first time in 1926 in Switzerland, and by C. H. Mayo in 1927. Both patients had had paroxysmal episodes of hypertension http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png JAMA American Medical Association

Clinical and Experimental Pheochromocytoma

JAMA , Volume 278 (1) – Jul 2, 1997

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Publisher
American Medical Association
Copyright
Copyright © 1997 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.
ISSN
0098-7484
eISSN
1538-3598
DOI
10.1001/jama.1997.03550010092050
Publisher site
See Article on Publisher Site

Abstract

The new edition of Clinical and Experimental Pheochromocytoma by Drs Manger and Gifford is a unique compendium and textbook on this topic. The first edition was written entirely by the principal authors, but a number of other investigators have contributed to the second edition. All are experts in their fields and deserve gratitude and respect for sharing their knowledge with the reader. In 1886 Frankel first described pheochromocytomas that were found at autopsy in both adrenal glands of an 18-year-old girl. In 1922, L'Abbé and his colleagues first made the fascinating observation that paroxysms of high blood pressure occurred in a young woman who was found at autopsy to have an adrenal tumor. Volhard had previously described the clinical syndrome. A pheochromocytoma was successfully removed by Roux the first time in 1926 in Switzerland, and by C. H. Mayo in 1927. Both patients had had paroxysmal episodes of hypertension

Journal

JAMAAmerican Medical Association

Published: Jul 2, 1997

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