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January 22, 2024European Heart Journal - Case ReportsOpen Access

Surgical resection of a rare cardiac paraganglioma in a 43-year-old woman led to clinical improvement from NYHA class III/IV to class I and LVEF recovery from 15% to 56% at 4 months.

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Why the study?

Paragangliomas are catecholamine-producing tumours that can arise from extra-adrenal chromaffin cells, but their occurrence in the heart is very rare.

Population

A 43-year-old woman with arterial hypertension, heart failure, and a cardiac mass

Comparison

Surgical resection of the tumour

Design

Case report

Follow-up

4 months

Key result

Surgical resection of a rare cardiac paraganglioma in a 43-year-old woman led to clinical improvement from NYHA class III/IV to class I and LVEF recovery from 15% to 56% at 4 months.

Authors

WTWikler Bernal TorresLVLeidy A Giraldo VinascoJGJuan Esteban Gómez‐Mesa

Discussion

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Member takes

Overview

May support resection in select cardiac paraganglioma cases with severe LV dysfunction; hypothesis-generating and requires validation in larger series.

Study Design

Type

Case Report (n=1)

Structured PICO

P
Population
A 43-year-old woman with a history of arterial hypertension presenting with severe heart failure symptoms due to a cardiac paraganglioma, followed for 4 months after surgical resection.
I
Intervention
Surgical resection of the tumour
O
Outcome
Clinical and echocardiographic improvement (NYHA class, LVEF, longitudinal strain)surrogate

Surgical resection of a rare cardiac paraganglioma can lead to dramatic recovery of severe left ventricular systolic dysfunction and heart failure symptoms.

Cite This Study

Torres et al. (2024) conducted a case report in Cardiac paraganglioma (n=1). Surgical resection was evaluated. Surgical resection of a rare cardiac paraganglioma in a 43-year-old woman led to clinical improvement from NYHA class III/IV to class I and LVEF recovery from 15% to 56% at 4 months.

synapsesocial.com/papers/6aaa18dfcf2bca5c547e6575https://doi.org/10.1093/ehjcr/ytae032
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