Natural history of a sporadic pheochromocytoma

Endocrine Practice

Volumn 14, Issue 3, 2008, Pages 391-

  Yu, Run ^a   Ginsburg, Eli ^a  

^a CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

(3 IODOBENZYL)GUANIDINE; ALDOSTERONE; CALCITONIN; CHROMOGRANIN A; HYDROCORTISONE; NORMETADRENALIN;

ADRENALECTOMY; AGED; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; HUMAN; LETTER; MALE; NEUROFIBROMATOSIS; PHEOCHROMOCYTOMA; VON HIPPEL LINDAU DISEASE; ADRENAL TUMOR; INCIDENTAL FINDING; NOTE; RADIOGRAPHY; TIME;

ADRENAL GLAND NEOPLASMS; ADRENALECTOMY; AGED; HUMANS; INCIDENTAL FINDINGS; MALE; PHEOCHROMOCYTOMA; TIME FACTORS; TOMOGRAPHY, X-RAY COMPUTED;

EID: 48949097200     PISSN: 1530891X     EISSN: None     Source Type: Journal    
DOI: 10.4158/EP.14.3.391     Document Type: Letter

References (2)

1. Magill SB, Fritsche CM, Klinger DE, Tector AJ, Shaker JL. Evolution of a pheochromocytoma. Endocr Pract. 2006;12:545-551.
2. Walther MM, Reiter R, Keiser HR, et al. Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma. J Urol. 1999;162(3 Pt 1):659-664.