Tumor Recurrence and Hypertension Persistence After Successful Pheochromocytoma Operation
- 1 May 1997
- journal article
- research article
- Published by Wolters Kluwer Health in Hypertension
- Vol. 29 (5) , 1133-1139
- https://doi.org/10.1161/01.hyp.29.5.1133
Abstract
Pheochromocytoma is a catecholamine-secreting tumor and a rare cause of hypertension that is usually curable. However, pheochromocytoma may recur as a benign or malignant tumor, and hypert...Keywords
This publication has 27 references indexed in Scilit:
- Evolving Concepts in the Pathophysiology, Diagnosis, and Treatment of PheochromocytomaEndocrine Reviews, 1994
- Pheochromocytomas, Multiple Endocrine Neoplasia Type 2, and von Hippel-Lindau DiseaseNew England Journal of Medicine, 1993
- Cardiac pheochromocytomasThe Annals of Thoracic Surgery, 1992
- Lisch Nodules in Neurofibromatosis Type 1New England Journal of Medicine, 1991
- Long‐term evaluation following resection of apparently benign pheochromocytoma(s)/paraganglioma(s)World Journal of Surgery, 1990
- MALIGNANT PHAEOCHROMOCYTOMA: CLINICAL, BIOCHEMICAL AND SCINTIGRAPHIC CHARACTERIZATIONClinical Endocrinology, 1984
- Biochemical tests for diagnosis of phaeochromocytoma: urinary versus plasma determinations.BMJ, 1981
- Analysis of urinary metanephrines by reversed-phase high-performance liquid chromatography and electrochemical detectionClinica Chimica Acta; International Journal of Clinical Chemistry, 1981
- Reporting results of cancer treatmentCancer, 1981
- Phaeochromocytomas in 72 patients: Clinical and diagnostic features, treatment and long term resultsBritish Journal of Surgery, 1979