Evidence map›Paper›PMID 40979823›Full record

ArticleJCEM case reports2025

Incidental Adrenal Hemangioma: A Diagnostic and Management Challenge.

Abhinay Jain, Alka Rana, Phibakordor L Nonglait, Pragya Mangla, Nishant Raizada, Sri Venkata Madhu

Abstract readCase Reports
In one paragraph

Article in JCEM case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

6 authors.

Abhinay JainDepartment of Endocrinology, University College of Medical Sciences and GTB Hospital, Delhi 110095, India.
Alka RanaDepartment of Pathology, Medanta-The Medicity Hospital, Gurugram 122001, India.
Phibakordor L NonglaitDepartment of Medicine, Civil Hospital, Shillong 793004, India.
Pragya ManglaDepartment of Endocrinology, University College of Medical Sciences and GTB Hospital, Delhi 110095, India.
Nishant RaizadaDepartment of Endocrinology, University College of Medical Sciences and GTB Hospital, Delhi 110095, India.
Sri Venkata MadhuDepartment of Endocrinology, University College of Medical Sciences and GTB Hospital, Delhi 110095, India.ORCID https://orcid.org/0000-0003-0018-5984

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adrenal hemangioma is a rare, benign vascular tumor often discovered incidentally during imaging. Here, we present the case of a 43-year-old male individual who was incidentally found to have a right adrenal mass during evaluation for polycythemia. Initial imaging revealed a 3.1 × 2.3 cm mass. The unenhanced computed tomography (CT) attenuation was 31 Hounsfield units (HU), and the post-contrast attenuation was approximately 61 HU. Hormonal evaluations, including cortisol, dehydroepiandrosterone sulfate (DHEA-S), aldosterone, renin, and metanephrines, were all within normal limits. The patient was managed conservatively, with close follow-up. Over the course of 2 years, the lesion remained stable in size until a sudden increase was noted, reaching 4.3 × 3.3 cm, with magnetic resonance imaging (MRI) revealing necrotic areas and peripheral enhancement. Due to the lesion's rapid growth and indeterminate features, the patient underwent a laparoscopic right adrenalectomy. The histopathological analysis confirmed the diagnosis of a cavernous adrenal hemangioma. This case emphasizes the importance of recognizing adrenal hemangiomas, as they can mimic more aggressive adrenal tumors and require careful monitoring.

Indexed as

adrenaladrenalectomyhemangiomatumor

Identifiers

PMID40979823
PMCPMC12448940

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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.