Evidence map›Paper›PMID 39986263›Full record

ArticleEndocrinology, diabetes & metabolism case reports2025

Resistant hypertension post-transsphenoidal surgery for pituitary Cushing's disease, leading to a diagnosis of primary aldosteronism.

Jack Lee, Maria Tomkins, Darran McDonald, Julie Martin-Grace, Claire Carthy, John Finnegan, Douglas Mulholland, Neal Dugal, Arnold D K Hill, Michael W O'Reilly and 1 more

Abstract read
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Article in Endocrinology, diabetes & metabolism case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Jack LeeAcademic Division of Endocrinology, Royal College of Surgeons in Ireland, Dublin, Ireland.ORCID https://orcid.org/0009-0005-7169-1974
Maria TomkinsAcademic Division of Endocrinology, Royal College of Surgeons in Ireland, Dublin, Ireland.
Darran McDonaldAcademic Division of Endocrinology, Royal College of Surgeons in Ireland, Dublin, Ireland.
Julie Martin-GraceAcademic Division of Endocrinology, Royal College of Surgeons in Ireland, Dublin, Ireland.
Claire CarthyDepartment of Endocrinology, Beaumont Hospital, Dublin, Ireland.
John FinneganDepartment of Interventional Radiology, Beaumont Hospital, Dublin, Ireland.
Douglas MulhollandDepartment of Interventional Radiology, Beaumont Hospital, Dublin, Ireland.
Neal DugalDepartment of Surgery, Beaumont Hospital, Dublin, Ireland.
Arnold D K HillDepartment of Surgery, Beaumont Hospital, Dublin, Ireland.
Michael W O'ReillyAcademic Division of Endocrinology, Royal College of Surgeons in Ireland, Dublin, Ireland.
Mark SherlockAcademic Division of Endocrinology, Royal College of Surgeons in Ireland, Dublin, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Summary: We describe a case of a 42-year-old gentleman, 5 years post-transsphenoidal surgery (TSS) for pituitary-dependent Cushing's disease, initially presenting with malignant hypertension. Despite an initial improvement in his blood pressure post-TSS, he was found to be persistently hypertensive on follow-up despite no clinical or biochemical evidence of recurrence of hypercortisolism. His blood pressure remained elevated despite five antihypertensive agents. His renin concentration was <5 mIU/L (9-103.5) and aldosterone concentration was 877 pmol/L (0-670). A subsequent CT of the adrenals showed a 1.2 cm left adrenal nodule. He was not suitable for adrenal vein sampling (AVS) at this time due to difficult-to-control hypertension. Biochemistry was difficult to interpret in the context of a multitude of interfering medications, which were necessary given his difficult-to-control hypertension and hypokalaemia. Once suitable, his initial AVS was unsuccessful due to failure to cannulate the right adrenal vein. He was given the further options of repeat AVS vs 11C-metomidate PET vs medical management of his blood pressure. He proceeded with a repeat AVS, with successful cannulation of both adrenal veins. This showed evidence of hyperaldosteronism on the left side, with a lateralisation index of 39.5 and a contralateral suppression index of 0.28. He proceeded with a robotic left adrenalectomy, leading to significant improvement in his blood pressure, dropping from a mean reading of 142/85 during daytime and 150/88 mmHg at nighttime on five antihypertensive agents to normotensive levels of 114/77 mmHg on two agents. Learning points: It is important to consider a broad differential for uncontrolled hypertension. It must be considered that patients can present with multiple, isolated endocrinopathies. There are diagnostic challenges with primary aldosteronism, with medication regimens regularly effecting suitability of testing and interpretation of results. AVS can be a challenging procedure, leading to diagnostic challenges in the lateralisation of primary aldosteronism; however, it or another form of lateralisation is essential to guide management options.

Indexed as

adrenalarticlescardiovascularcasesrare diseases/syndromes

Identifiers

PMID39986263
PMCPMC11883862

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