Radiopharmaceutical Treatment of Pheochromocytomas
نویسندگان
چکیده
منابع مشابه
Tumor Markers in Pheochromocytomas
.........................................................................................................................................................10 INTRODUCTION................................................................................................................................................11 REVIEW OF THE LITERATURE.............................................................
متن کاملMolecular markers of paragangliomas/pheochromocytomas
Paragangliomas/pheochromocytomas comprise rare tumors that arise from the extra-adrenal paraganglia, with an incidence of about 2 to 8 per million people each year. Approximately 40% of cases are due to genetic mutations in at least one out of more than 30 causative genes. About 25-30% of pheochromocytomas/paragangliomas develop under the conditions of a hereditary tumor syndrome a third of whi...
متن کاملPheochromocytomas and secreting paragangliomas
Catecholamine-producing tumors may arise in the adrenal medulla (pheochromocytomas) or in extraadrenal chromaffin cells (secreting paragangliomas). Their prevalence is about 0.1% in patients with hypertension and 4% in patients with a fortuitously discovered adrenal mass. An increase in the production of catecholamines causes symptoms (mainly headaches, palpitations and excess sweating) and sig...
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ژورنال
عنوان ژورنال: Annals of the New York Academy of Sciences
سال: 2002
ISSN: 0077-8923,1749-6632
DOI: 10.1111/j.1749-6632.2002.tb04412.x