Resistant hypertension - pheochromocytoma

We 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.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:109

Enthalten in:

Laeknabladid - 109(2023), 3 vom: 09. März, Seite 141-145

Sprache:

Isländisch

Beteiligte Personen:

Jonsson, Krister Blaer [VerfasserIn]
Gudmundsson, Eirikur Orri [VerfasserIn]
Sigurdardottir, Margret [VerfasserIn]
Jonsson, Jon Johannes [VerfasserIn]
Sigurjonsdottir, Helga Agusta [VerfasserIn]

Links:

Volltext

Themen:

Case Reports
English Abstract
Journal Article
Metanephrine
Neuroendocrine tumor
Paraganglioma
Pheochromocytoma
Resistant hypertension

Anmerkungen:

Date Completed 03.03.2023

Date Revised 03.03.2023

published: Print

Citation Status MEDLINE

doi:

10.17992/lbl.2023.03.735

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM353624810