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  1. Home
  2. Keyword: Tuberous Sclerosis/complications
Figure 1
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Editorial

Has the Natural History of Primary Heart Tumors in Children Been Modified Recently?

Vera Demarchi Aiello

Morphology of the nodular lesions of the fetal and neonatal heart

The most frequent nodular lesions of the fetal and neonatal heart are rhabdomyomas and fibromas, which are considered hamartomas.

In rhabdomyoma cells, the lack of proliferative immunohistochemical markers indicates that these lesions are more likely hamartomas rather than true neoplasms.

[…]

  • Child
  • Fetal Heart/abnormalities
  • Fetus/diagnosis imaging
  • Heart Neoplasms/pathology
  • Tuberous Sclerosis/complications
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Creative Commons Attribution (CC BY) Creative Commons license
18/03/2024 DOI: 10.36660/abc.20230849
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Tuberous Sclerosis: Unusual Findings in the Setting of a Rare Disease

Ines Oliveira et al. Rafaela Lopes Isabel Cruz Bruno Bragança … João Azevedo Aurora Andrade

Case Description

A 40-year-old woman diagnosed with tuberous sclerosis (TS) at the age of one, with cognitive impairment, epilepsy and renal angiomyolipomas, was referred to Cardiology for complaints of fatigue. She had no known family history of TS. Although her mother could not confirm if a genetic test had been performed, the patient had a definite diagnosis of TS, according to International Tuberous Sclerosis Consensus Group revised criteria, due to the presence of several major criteria, as hypomelanotic macules, facial angiofibromas, cortical dysplasia and subependymal nodules.

On cardiovascular evaluation, she had no dyspnea on exertion, chest pain, palpitations or history of syncope. On physical examination, she had multiple cutaneous angiofibromas and hypomelanotic macules, cardiac auscultation with no murmurs or signs of congestion. Electrocardiogram (ECG) showed nonspecific repolarization abnormalities ( ) and no arrhythmic events were detected by the Holter method. Transthoracic echocardiography revealed the presence of multiple intracardiac hyperechogenic lesions, with no blood flow obstruction or valvular impairment, and preserved ventricular systolic function ( ). Cardiac magnetic resonance (CMR) showed the nature of the lesions ( ) – homogeneous high signal intensity in T1 and T2-weighted images (A, B, C), with uniform suppression with the application of fat-saturation pulses, with an intensity similar to adipose tissue (D). The lesions also showed chemical shift , revealing its lipomatous nature (F). No evidence of perfusion, late gadolinium enhancement (E) or other masses. The patient remained asymptomatic after five years of follow-up, performing an annual ECG and echocardiogram, with no increase in the number or size of lipomas.

[…]

  • Atherosclerosis
  • Diagnostic Imaging
  • Familial Multiple Lipomatosis
  • Neoplasms
  • Tuberous Sclerosis/complications
  • Tumor Supressor/genetics
Read Full Article
Creative Commons Attribution (CC BY) Creative Commons license
13/02/2023 DOI: 10.36660/abc.20220147

How to cite this article

EndNote RIS

Electronic Document Format (Vancouver)

Aiello VD. Has the Natural History of Primary Heart Tumors in Children Been Modified Recently?. Arquivos Brasileiros de Cardiologia 2024;121(1):e20230849.

Electronic Document Format (ABNT)

Aiello, Vera Demarchi. Has the Natural History of Primary Heart Tumors in Children Been Modified Recently?. Arquivos Brasileiros de Cardiologia, v. 121, n. 1, e20230849, Mar. 2024.

Electronic Document Format (APA)

Aiello, V. D. (2024). Has the Natural History of Primary Heart Tumors in Children Been Modified Recently?. Arquivos Brasileiros de Cardiologia, 121(1), e20230849.

Electronic Document Format (ISO)

Aiello, Vera Demarchi. Has the Natural History of Primary Heart Tumors in Children Been Modified Recently?. Arquivos Brasileiros de Cardiologia [online]. 2024, vol. 121, n. 1, [cited 2026-10-14], e20230849. Available from: <https://journals.cardiol.br/en/article/has-the-natural-history-of-primary-heart-tumors-in-children-been-modified-recently/>. ISSN 0066-782X

EndNote RIS

Electronic Document Format (Vancouver)

Oliveira I, Lopes R, Cruz I, Bragança B, Azevedo J, Andrade A. Tuberous Sclerosis: Unusual Findings in the Setting of a Rare Disease. Arquivos Brasileiros de Cardiologia 2023;120(1):e20220147.

Electronic Document Format (ABNT)

Oliveira, Ines; Lopes, Rafaela; Cruz, Isabel; Bragança, Bruno; Azevedo, João; Andrade, Aurora. Tuberous Sclerosis: Unusual Findings in the Setting of a Rare Disease. Arquivos Brasileiros de Cardiologia, v. 120, n. 1, e20220147, Feb. 2023.

Electronic Document Format (APA)

Oliveira, I., Lopes, R., Cruz, I., Bragança, B., Azevedo, J., & Andrade, A. (2023). Tuberous Sclerosis: Unusual Findings in the Setting of a Rare Disease. Arquivos Brasileiros de Cardiologia, 120(1), e20220147.

Electronic Document Format (ISO)

Oliveira, Ines and Lopes, Rafaela and Cruz, Isabel and Bragança, Bruno and Azevedo, João and Andrade, Aurora. Tuberous Sclerosis: Unusual Findings in the Setting of a Rare Disease. Arquivos Brasileiros de Cardiologia [online]. 2023, vol. 120, n. 1, [cited 2026-10-14], e20220147. Available from: <https://journals.cardiol.br/en/article/tuberous-sclerosis-unusual-findings-in-the-setting-of-a-rare-disease/>. ISSN 0066-782X

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