Young asthmatic woman with dyspnea of very unusual etiology

Authors

  • Miguel Ángel Barón-Ramos Unidad de Gestión de Medicina Interna, Hospital de la Serranía de Ronda, Málaga, Spain
  • María Aurora Ruz-Zafra Unidad de Gestión de Medicina Interna, Hospital de la Serranía de Ronda, Málaga, Spain
  • María Ángeles González-Benítez Unidad de Gestión de Medicina Interna, Hospital de la Serranía de Ronda, Málaga, Spain
  • Irene Pernía-Rodríguez Unidad de Gestión de Medicina Interna, Hospital de la Serranía de Ronda, Málaga, Spain
  • Alberto Ruiz-Cantero Unidad de Gestión de Medicina Interna, Hospital de la Serranía de Ronda, Málaga, Spain

DOI:

https://doi.org/10.32818/reccmi.a4n1a8

Keywords:

rare tumors, cardiac tumors, myxofibrosarcoma, cardiac sarcoma.

Abstract

We present the case of a 36-year-old woman with a history of bronchial asthma who presented progressive dyspnea without improvement, despite intensive steroid and bronchodilator treatment. In view of the multiple consultations in the Emergency Room, admission to Internal Medicine was decided for study. After the initial approach, and always focused on his asthmatic background, it was a surprise to find the true cause of dyspnea: an infiltrating malignant cardiac tumor of the left atrium of sarcomatous lineage, which despite being operated on, led the patient to death.

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References

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Published

2019-04-30

How to Cite

1.
Barón-Ramos M Ángel, Ruz-Zafra MA, González-Benítez M Ángeles, Pernía-Rodríguez I, Ruiz-Cantero A. Young asthmatic woman with dyspnea of very unusual etiology. Rev Esp Casos Clin Med Intern [Internet]. 2019 Apr. 30 [cited 2024 Dec. 26];4(1):21-3. Available from: https://www.reccmi.com/RECCMI/article/view/351

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