Evidence map›Paper›PMID 38026486›Full record

ArticleFrontiers in surgery2023

Rare adrenal cavernous hemangioma: a case report highlighting diagnostic challenges.

Ryan Michael Antar, Christian Mark Farag, Kirolos Youssef, Vincent Xu, Arthur Drouaud, Noah Panitch, Zoon Tariq, Ali Alzeer, Michael J Whalen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in surgery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. An imaging and diagnostic conundrum-the adrenal haemangioma.Journal of surgical case reports · 2024
    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

9 authors at 1 institution in 1 country.

Ryan Michael AntarDepartment of Urology, George Washington University School of Medicine, Washington, DC, United States.
Christian Mark FaragDepartment of Medicine, George Washington University School of Medicine, Washington, DC, United States.
Kirolos YoussefDepartment of Urology, George Washington University School of Medicine, Washington, DC, United States.
Vincent XuDepartment of Urology, George Washington University School of Medicine, Washington, DC, United States.
Arthur DrouaudDepartment of Urology, George Washington University School of Medicine, Washington, DC, United States.
Noah PanitchDepartment of Urology, George Washington University School of Medicine, Washington, DC, United States.
Zoon TariqDepartment of Pathology, George Washington University School of Medicine, Washington, DC, United States.
Ali AlzeerDepartment of Pathology, George Washington University School of Medicine, Washington, DC, United States.
Michael J WhalenDepartment of Urology, George Washington University School of Medicine, Washington, DC, United States.
George Washington University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Adrenal cavernous hemangiomas are rare benign vascular tumors that pose significant diagnostic challenges. Despite their benign nature, features overlapping with malignancies often complicate management decisions. Case presentation: A 64-year-old male presented with a 4.4 cm necrotic left adrenal mass discovered incidentally on imaging. His medical history included papillary thyroid carcinoma, with subsequent thyroidectomy and radioactive iodine ablation. Evaluations for hiccups revealed multiple lung nodules, hypertrophic cardiomyopathy, and anemia. Given the patient's previous cancer history, elevated aldosterone/renin ratio, and mass size, our multidisciplinary tumor board decided to proceed with a left adrenalectomy. Post-surgical pathology confirmed a diagnosis of adrenal cavernous hemangioma. Conclusion: The occurrence of ambiguous adrenal mass with other pathologies, such as our patient's papillary thyroid carcinoma, complicates the diagnostic and therapeutic landscape. As demonstrated in our case, opting for surgery remains a viable solution for adrenal cavernous hemangiomas, especially for masses greater than 4 cm. Interdisciplinary collaboration, exemplified by our tumor board's decision-making process, is crucial for optimal management. This case underscores the need for a multifaceted approach when confronting adrenal masses with such diagnostic ambiguity.

Indexed as

adrenalectomyadrenal massadrenalomacavernous hemangiomahemangiomaincidentaloma

Identifiers

PMID38026486
PMCPMC10667707
OpenAlexW4388638563

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.