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- Krister Blaer Jonsson, Eirikur Orri Gudmundsson, Margret Sigurdardottir, Jon Johannes Jonsson, and Helga Agusta Sigurjonsdottir.
- Faculty of Medicine, University of Iceland.
- Laeknabladid. 2023 Mar 1; 109 (3): 141145141-145.
AbstractWe report a case of a man with a 30-year history of treatment-resistant hypertension, hydropoiesis, tachycardic spells and dysgeusia. Despite repeated visits to the emergency department and work-up in an out-patient clinic, the diagnosis was unknown. Three years prior to remittance to an endocrinologist, the hypertension worsened, and he developed diabetes type-II. Further work-up revealed a 3 cm extra-adrenal pheochromocytoma, a paraganglioma. After surgical removal of the tumor, he is without medication and symptom free. Pheochromocytoma and paraganglioma are rare causes of hypertension, estimated to explain 0.1-0.6% of all cases, but nonetheless an important diagnosis to make, due to serious side effects.
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