Evidence map›Paper›PMID 41043910›Full record

ArticleJACC. Case reports2025

Unusual-Appearing Calcified Left Atrial Myxoma.

Paige Holden, Akshat Banga, Paul VanderLaan, Kyle Pond, Louis Chu

Abstract readCase Reports
In one paragraph

Article in JACC. Case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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.

Paige HoldenDepartment of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Akshat BangaDepartment of Medicine, Mount Auburn Hospital, Harvard Medical School, Cambridge, Massachusetts, USA.
Paul VanderLaanDepartment of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Kyle PondDepartment of Medicine, Mount Auburn Hospital, Harvard Medical School, Cambridge, Massachusetts, USA; Department of Cardiology, Mount Auburn Hospital, Harvard Medical School, Cambridge, Massachusetts, USA.
Louis ChuDepartment of Cardiothoracic Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA. Electronic address: lchu@bidmc.harvard.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiac myxoma is a rare tumor with variability in clinical presentation, imaging, and histopathologic findings. CASE SUMMARY: An 82-year-old woman presented with fatigue, dizziness, and declining exercise tolerance. Work-up included echocardiogram notable for an atrial mass. Further imaging diagnosed left atrial myxoma for which she underwent open surgical resection. DISCUSSION: Cardiac myxomas with gross calcifications are uncommon and are usually seen in right rather than left atrial tumors. The pathogenesis of their formation is largely unknown. We present a rare case of a left atrial myxoma with large, dystrophic calcifications that affected both preoperative and intraoperative evaluation of the tumor. TAKE-HOME MESSAGES: Cardiac myxoma tumor characteristics are quite variable, with gross calcifications generally uncommon and more frequently seen in the right rather than the left atrium. Supplemental imaging such as cardiac magnetic resonance may be necessary in preoperative evaluation of heavily calcified cardiac tumors owing to limitations in echocardiographic images regarding sufficient diagnostic detail.

Indexed as

calcificationcardiac magnetic resonancecardiac myxomaechocardiographyhistopathologyimaging

Identifiers

PMID41043910
PMCPMC12540285

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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.