Evidence map›Paper›PMID 41467148›Full record

ArticleAACE endocrinology and diabetes

Giant Prolactinoma: Challenges in Management.

Sapna Sharma, Madhav Acharya, Chheki Sherpa

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. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

3 authors.

Sapna SharmaDepartment of Endocrinology, Diabetes and Metabolism, Tower Health/Reading Hospital, Reading, Pennsylvania.
Madhav AcharyaDepartment of Endocrinology, Diabetes and Metabolism, Tower Health/Reading Hospital, Reading, Pennsylvania.
Chheki SherpaDepartment of Endocrinology, Diabetes and Metabolism, Tower Health/Reading Hospital, Reading, Pennsylvania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Objective: Prolactinomas are the most common form of pituitary adenomas, 90% of which are microprolactinomas measuring <1 cm. A giant prolactinoma is defined as a prolactinoma measuring >4 cm with a serum prolactin level of >1000 ng/mL. We report a case of giant prolactinoma causing optic nerve compression that initially responded well to cabergoline and later developed intratumoral hemorrhage requiring transsphenoidal resection. Case Report: A 47-year-old man presented with blurry vision and intermittent headaches for 6 months. Visual field (VF) testing demonstrated bitemporal VF defect, which prompted magnetic resonance imaging of brain that showed a 4.1 × 3.1 × 3.1-cm pituitary macroadenoma with suprasellar extension compressing the optic chiasm. Laboratory evaluation revealed an increased prolactin level, low testosterone level, inappropriately normal luteinizing hormone level, and follicle-stimulating hormone level consistent with central hypogonadism. Cabergoline 0.5 mg twice weekly was started. Repeat VF testing and prolactin level in 4 weeks after starting cabergoline showed improvement. Nine months later, his symptoms worsened, and repeat magnetic resonance imaging showed intratumoral hemorrhage and that the size of the tumor had increased. He underwent an emergent transsphenoidal resection. After surgery, he developed central adrenal insufficiency and central hypothyroidism requiring steroid and thyroid hormone replacement. Discussion: Only a few cases of giant prolactinomas have been reported, and no clear guidelines for management of giant prolactinomas have been established. First-line medical management includes dopamine agonists such as cabergoline and bromocriptine. Conclusion: The dilemma between medical management and surgical management occurs during initial presentation of giant prolactinoma with VF defect. Our case report highlights the challenges and complications encountered in the treatment of a patient with giant prolactinoma.

Indexed as

apoplexycabergolinecentral hypogonadismgiant prolactinomapituitary tumortranssphenoidal surgerytreatment resistancevisual field defect

Identifiers

PMID41467148
PMCPMC12744783

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