Case Report


A clinical challenge of cardiomyopathies: Beyond the heart

,  ,  ,  ,  

1 Internal Medicine Service, Medicine Department, Pedro Hispano Hospital, Matosinhos, Porto, Portugal

2 Cardiology Service, Álvaro Cunqueiro Hospital, Vigo, Spain

Address correspondence to:

Dina Fernandes Neto

Internal Medicine Service, Medicine Department, Pedro Hispano Hospital, Matosinhos, Porto,

Portugal

Message to Corresponding Author


Article ID: 101434Z01DZ2024

doi: 10.5348/101434Z01DZ2024CR

Access full text article on other devices

Access PDF of article on other devices

How to cite this article

Neto DF, Zhygalova I, Melendo-Viu M, Dobarro D, Romo AI. A clinical challenge of cardiomyopathies: Beyond the heart. Int J Case Rep Images 2024;15(1):1–5.

ABSTRACT


Introduction: The relation between the cancer and the heart is diverse. It can be affected all parts of the heart directly or indirectly caused by the systemic manifestation of the cancer or by cancer therapy. Paraneoplastic dermatomyositis and tumor lysis syndrome (TLS) are two examples of systemic manifestations of cancer. Being systemic, the cardiovascular system can be affected. Heart failure and arrhythmias are the main cardiac manifestations.

Case Report: A 68-year-old man with a recent diagnosis of diffuse large B-cell lymphoma waiting to begin chemotherapy, and paraneoplastic dermatomyositis, presented at the emergency department (ED) with palpitations and dyspnea with a week of evolution. At the physical examination, he presented with pulmonary edema and the novo rapid atrial fibrillation. Also, an Nt-pro BNP of 8957 pg/mL, and echocardiography with severe dilated left ventricle, with a severe reduced ejection fraction. Already in the ward, the patient developed a spontaneous TLS. The etiological interpretation was that paraneoplastic dermatomyositis and TLS were the triggers of atrial fibrillation (AF). Then, the combination of them was responsible for development of the dilated cardiomyopathy (tachymyocardiopathy). The chemotherapy regimen was changed to R-CEOP (Rituximab, cyclophosphamide, etoposide, vincristine sulfate, and prednisone).

Conclusion: This clinical case perfectly shows how the world of cardiomyopathies can be challenging and hard to understand all the complexity of the patients.

Keywords: Cardiomyopathy, Heart failure, Paraneoplastic dermatomyositis, Tumor lysis syndrome

SUPPORTING INFORMATION


Author Contributions

Dina Fernandes Neto - Substantial contributions to conception and design, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published

I Zhygalova - Substantial contributions to conception and design, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published

M Melendo-Viu - Substantial contributions to conception and design, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published

D Dobarro - Substantial contributions to conception and design, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published

A Iñiguez Romo - Substantial contributions to conception and design, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published

Guarantor of Submission

The corresponding author is the guarantor of submission.

Source of Support

None

Consent Statement

Written informed consent was obtained from the patient for publication of this article.

Data Availability

All relevant data are within the paper and its Supporting Information files.

Conflict of Interest

Authors declare no conflict of interest.

Copyright

© 2024 Dina Fernandes Neto et al.. This article is distributed under the terms of Creative Commons Attribution License which permits unrestricted use, distribution and reproduction in any medium provided the original author(s) and original publisher are properly credited. Please see the copyright policy on the journal website for more information.


Comment on Article