Evidence map›Paper›PMID 40255443›Full record

ArticleJCEM case reports2025

Familial Paraganglioma Presenting With Acute Coronary Syndrome and Coronary Vasospasm.

Carlos Puig-Jové, Luis García Pascual, Verónica Perea, Carmen Quirós, Andreu Simó-Servat, María-José Barahona

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. 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

6 authors.

Carlos Puig-JovéEndocrinology and Nutrition Department, Hospital Universitari Mútua Terrassa, Terrassa 08221, Spain.ORCID https://orcid.org/0000-0001-9466-2627
Luis García PascualEndocrinology and Nutrition Department, Hospital Universitari Mútua Terrassa, Terrassa 08221, Spain.
Verónica PereaEndocrinology and Nutrition Department, Hospital Universitari Mútua Terrassa, Terrassa 08221, Spain.ORCID https://orcid.org/0000-0001-8104-7326
Carmen QuirósEndocrinology and Nutrition Department, Hospital Universitari Mútua Terrassa, Terrassa 08221, Spain.
Andreu Simó-ServatEndocrinology and Nutrition Department, Hospital Universitari Mútua Terrassa, Terrassa 08221, Spain.
María-José BarahonaEndocrinology and Nutrition Department, Hospital Universitari Mútua Terrassa, Terrassa 08221, Spain.ORCID https://orcid.org/0000-0003-2935-6521

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial paraganglioma syndrome (FPS) is a rare genetic disorder characterized by the development of paragangliomas (PGLs) and pheochromocytomas (PCCs). Here, we describe the case of a 42-year-old man with a family history of FPS, who presented with episodic chest pain and was diagnosed with acute coronary syndrome secondary to cardiac PGL-induced vasospasm. A thorough review of the family history confirmed several cases of PGLs and PCCs in the immediate family circle. A pathogenic variant in the succinate dehydrogenase (

Indexed as

cardiac paragangliomafamilial paraganglioma syndromevasospasm

Identifiers

PMID40255443
PMCPMC12006788

What OpenQuestion holds

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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.