ReviewHigh blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension2018
Secondary Arterial Hypertension: From Routine Clinical Practice to Evidence in Patients with Adrenal Tumor.
Review in High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 19 citations in OpenAlex.
- Non-incidentally detected adrenal mass: a paradigm shift beyond incidentaloma?Journal of endocrinological investigation · 2026Article
- A combined encoder-transformer-decoder network for volumetric segmentation of adrenal tumors.Biomedical engineering online · 2023Article
- CT Texture Analysis of Adrenal Pheochromocytomas: A Pilot Study.Current oncology (Toronto, Ont.) · 2023Article
- Editorial: Predictive tools in pheochromocytoma and paraganglioma.Frontiers in endocrinology · 2023Article
- Frequently asked questions and answers (if any) in patients with adrenal incidentaloma.Journal of endocrinological investigation · 2021Review
- Endocrine hypertension secondary to adrenal tumors: clinical course and predictive factors of clinical remission.Langenbeck's archives of surgery · 2021Article
- Autonomous cortisol secretion in adrenal incidentalomas.Endocrine · 2019Review
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
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Abstract
Prevalence of arterial hypertension is up to 30-40% in epidemiological studies, it increases with aging and affects the cardiovascular risk. Essential form of hypertension is the most frequent; however, 5-10% of patients are affected by a specific and potentially reversible cause of increased blood pressure levels, called secondary hypertension. In general, all patients with young onset-age (< 40-50 years) or resistant hypertension should be screened for secondary forms. Among them, primary aldosteronism, Cushing's Syndrome and pheochromocytoma are the most common cause of endocrine hypertension associated with an autonomous secretion of adrenal hormones, often secondary to a tumor (either mono- or bi-lateral, or not always in the adrenals). Their diagnosis could be challenging, especially in patients with hypertension as the first (and/or isolated) clinical manifestation. Moreover, they are all rare form of hypertension, therefore a correct screening with a sensitive test is mandatory, to refer quickly the patients to an Endocrine Unit. In this short review we pinpoint our attention to these adrenal-related secondary form of hypertension, describing in a concise way their first-line screening procedures.
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