Case studies

Pheochromocytomas/Paragangliomas and two cases

W. van Vuuren, N.E. Nyakale, F.S.J. Naude, B.J. Meyer, M.M. Sathekge
South African Family Practice | Vol 49, No 5 : June| a849 | DOI: https://doi.org/10.1080/20786204.2007.10873557 | ©
Submitted: 26 June 2007 | Published: 30 June 2007

About the author(s)

W. van Vuuren, University of Pretoria, South Africa
N.E. Nyakale, University of Pretoria, South Africa
F.S.J. Naude, University of Pretoria, South Africa
B.J. Meyer, University of Pretoria, South Africa
M.M. Sathekge, University of Pretoria, South Africa

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Abstract

Pheochromocytomas are catecholamine-producing neuroendocrine tumours that arise from the adrenal medulla or extramedullary pheochromoblasts with highly variable clinical presentation, including episodes of headache, sweating, palpitations and hypertension. Due to the non-specificity of the symptoms there is usually a delay between the onset of symptoms and the final diagnosis. To make a firm diagnosis, biochemical testing of the blood (catecholamines) or urine (metanephrines and VMA) are mandatory. Many stimuli increase circulating catecholamines and metabolites and must receive due attention to prevent false-positive results. Therapeutically, surgery is the gold standard. To minimise complications during and post surgery the lesion(s) should be carefully localised via imaging studies. Adequate pre- and postoperative medical treatment is important. The history, diagnosis and therapy of two patients—the one with a paraganglioma of the organ of Zuckerkandl, the other with a intra thoracic paraganglioma are presented.

Keywords

pheochromocytomas; paragangliomas

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