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Pheochromocytoma — A Discussion of Symptoms, Signs and Procedures of Diagnostic Value

List of authors.
  • Reginald H. Smithwick, M.D.,
  • William E. R. Greer, M.D.,
  • Charles W. Robertson, M.D.§,
  • and Robert W. Wilkins, M.D.

PHEOCHROMOCYTOMAS are rare tumors that may cause any known form of hypertension. Although the hypertension may be and most commonly is paroxysmal, it may also be nonparoxysmal. In either case, the hypertension may be intermittent or persistent. Pheochromocytomas develop from chromaffin tissue and consequently are found wherever this occurs. The most common location is the medullary portion of the adrenal gland. Tumors also arise from sympathetic-ganglion tissue and consequently may be found in various locations. The most common site of origin other than the adrenal gland is the organ of Zuckerkandl, which is located just above the aortic bifurcation. In . . .

Funding and Disclosures

* Presented at the annual meeting of the New England Surgical Society, Bretton Woods, New Hampshire, September 23, 1949.

From the Medical and Surgical Services, Massachusetts Memorial Hospitals, and the Departments of Medicine and Surgery, Boston University School of Medicine.

Author Affiliations

†Professor of surgery, Boston University School of Medicine; surgeon-in-chief, Massachusetts Memorial Hospitals.

‡Instructor of medicine, Boston University School of Medicine; chief resident, Medical Service, Massachusetts Memorial Hospitals.

§Instructor of surgery, Boston University School of Medicine; assistant visiting surgeon, Massachusetts Memorial Hospitals.

¶Associate professor of medicine, Boston University School of Medicine; assistant director, Evans Memorial, Massachusetts Memorial Hospitals.

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