Evidence map›Paper›PMID 41467134›Full record

ArticleAACE endocrinology and diabetes

Primary Empty Sella Presenting With Anterior Hypopituitarism: Reframing a Benign Radiologic Finding Through Its Endocrine Consequences.

Emmeline Monique T Ngo

Abstract readCase Reports
In one paragraph

Article in AACE endocrinology and diabetes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Emmeline Monique T NgoSection of Endocrinology, Diabetes, and Metabolism - Department of Medicine, University of Missouri-Kansas City, Kansas City, Missouri.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Objective: Primary empty sella (ES) is typically considered a benign incidental radiologic finding characterized by herniation of the subarachnoid space into the sella turcica and flattening of the pituitary gland. Emerging evidence suggests ES can be associated with varying degrees of clinically significant pituitary dysfunction, which is often underrecognized. We present a case highlighting the endocrine implications of ES and the need for comprehensive evaluation. Case Report: A 53-year-old woman was referred for abnormal thyroid function tests found on routine screening. She reported fatigue, cold intolerance, and cognitive slowing. Laboratory evaluation revealed central hypothyroidism, and a subsequent evaluation of anterior pituitary function revealed central adrenal insufficiency, hypogonadotropic hypogonadism, and growth hormone deficiency. There was no evidence of arginine vasopressin deficiency. Magnetic resonance imaging showed a primary ES with no visualized pituitary gland. Initiation of hormone replacement therapy subsequently resulted in significant clinical improvement. Discussion: This case illustrates that ES may represent a radiologic marker of evolving anterior hypopituitarism, rather than a benign variant. Without appropriate endocrine evaluation, such cases may be misdiagnosed or untreated, leading to worsened morbidity. Given the increasing use of advanced neuroimaging, incidental detection of ES is rising, making awareness of its potential endocrine consequences timely and relevant. Clinical vigilance and comprehensive endocrine assessment are essential to avoid delayed diagnosis and complications. Conclusion: Primary ES may herald progressive pituitary dysfunction. Clinicians should maintain a high index of suspicion and evaluate for central hormonal deficits when primary ES is identified incidentally.

Indexed as

anterior hypopituitarismempty sellapituitary

Identifiers

PMID41467134
PMCPMC12744797

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.