Evidence map›Paper›PMID 40470420›Full record

ArticleCureus2025

Pituitary Apoplexy Following Gonadotropin-Releasing Hormone Agonist Therapy: A Rare and Life-Threatening Complication.

Aytan Naghiyeva, Nadia Smati, Calixto-Hope G Lucas, Brandi R Page, Mihail Zilbermint

Abstract readCase Reports
In one paragraph

Article in Cureus, 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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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Aytan NaghiyevaDepartment of Endocrinology, Diabetes, and Metabolism, Ege Hospital, Baku, AZE.
Nadia SmatiDepartment of Internal Medicine, Kaiser Permanente, Gaithersburg, USA.
Calixto-Hope G LucasDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, USA.
Brandi R PageDepartment of Head and Neck Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, USA.
Mihail ZilbermintDivision of Hospital Medicine, Johns Hopkins Community Physicians, Baltimore, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pituitary apoplexy is a rare but potentially life-threatening endocrine emergency characterized by acute hemorrhage or infarction of the pituitary gland. While often associated with pre-existing adenomas, it may also occur in previously normal glands. Risk factors include surgery, pregnancy, and medications such as gonadotropin-releasing hormone (GnRH) agonists, which are rarely implicated in pituitary apoplexy. We present the case of a 59-year-old male with a history of type 2 diabetes mellitus, hypertension, hyperlipidemia, and prostate cancer who developed intractable headache, nausea, vomiting, photophobia, and blurred vision shortly after receiving a leuprolide, GnRH agonist injection, for the treatment of prostate cancer. Brain imaging revealed a sellar and suprasellar pituitary tumor with hemorrhage. He was treated with intravenous fluids and steroids. The patient underwent emergent transsphenoidal hypophysectomy surgery, and pathology confirmed a gonadotroph adenoma with necrosis. The patient was discharged in stable condition. Pituitary apoplexy following GnRH agonist therapy is exceedingly rare, with fewer than 30 cases reported in the public domain. Proposed mechanisms include sudden cell shrinkage and metabolic hyperactivity within the pituitary gland. This case underscores the importance of recognizing the clinical presentation of pituitary apoplexy, as timely diagnosis and treatment are crucial to preventing severe neurological and endocrine sequelae. Clinicians should maintain a high index of suspicion for pituitary apoplexy in patients presenting with acute neurological or endocrine symptoms following GnRH agonist therapy. Increased awareness and vigilance in at-risk populations are essential, as routine pre-screening for pituitary adenomas is not currently standard practice.

Indexed as

gnrh agonistgonadotroph adenomagonadotropin-releasing hormone (gnrh)leuprolidepituitary apoplexytranssphenoidal pituitary surgery

Identifiers

PMID40470420
PMCPMC12136544

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