| Literature DB >> 18689909 |
E M Abma1, P M Kluin, R P F Dullaart.
Abstract
We describe a case of hypokalaemic hypertension due to hyperaldosteronism caused by a unilateral adrenocortical tumour with unfavourable histopathology suggestive of malignancy. After removal, the aldosterone excess disappeared. The patient's clinical course was uneventful, until she presented with extensive metastases of adrenal carcinoma four years later. Biochemical abnormalities were now consistent with glucocorticoid excess without hyperaldosteronism. She died four months later. Although malignant aldosterone-producing adrenal tumours are very rare, the present case underscores that clinicians should be aware that primary hyperaldosteronism can occur in the context of adrenocortical carcinoma.Entities:
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Year: 2008 PMID: 18689909
Source DB: PubMed Journal: Neth J Med ISSN: 0300-2977 Impact factor: 1.422