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Unusual Presentation of Atrial Myxoma: A Case Report and Review of the Literature

Patient: Female, 40-year-old Final Diagnosis: Atrial myxoma • myocardial infarction Symptoms: Dry cough • shortness of breath • wheezing Medication: — Clinical Procedure: — Specialty: Cardiology • Pathology • Pulmonology OBJECTIVE: Unusual clinical course BACKGROUND: Although rare, atrial myxoma is...

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Detalles Bibliográficos
Autores principales: Jaravaza, Diana Rufaro, Lalla, Usha, Zaharie, Stefan Dan, de Jager, Louis Johann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8105743/
https://www.ncbi.nlm.nih.gov/pubmed/33939684
http://dx.doi.org/10.12659/AJCR.931437
Descripción
Sumario:Patient: Female, 40-year-old Final Diagnosis: Atrial myxoma • myocardial infarction Symptoms: Dry cough • shortness of breath • wheezing Medication: — Clinical Procedure: — Specialty: Cardiology • Pathology • Pulmonology OBJECTIVE: Unusual clinical course BACKGROUND: Although rare, atrial myxoma is the most common benign cardiac tumor. The recognized triad of presenting symptoms relates to constitutional, embolic, and obstructive effects produced by the tumor. However, the presentation may be non-specific and mimic other diseases, confounding diagnosis. CASE REPORT: A middle-aged woman presented with wheezing and shortness of breath. With a strong background smoking history, the initial impression was that of acute bronchospasm. She however deteriorated rapidly, with decreased consciousness and cardiac arrest requiring resuscitation. Despite intensive care management, she died within 1 day of admission. Autopsy revealed a previously undiagnosed left atrial myxoma with coronary and systemic embolization. CONCLUSIONS: This case highlights an unusual presentation of atrial myxoma, resulting in fatal simultaneous embolization to the coronary and cerebral arteries. This simultaneous embolic presentation is not common, but the potential consequences are serious. This report also demonstrates that the presentation of a left-sided atrial myxoma with cardiac asthma can mimic respiratory disease and confound diagnosis. In adult patients without a history of chronic respiratory disease, the possibility of cardiac asthma should always be entertained. Furthermore, the importance of considering atrial myxoma as a cause for cardiac asthma is emphasized. The use of transthoracic echocardiogram in aiding the rapid diagnosis of atrial myxoma is recommended. Finally, the continued acknowledgement of the important contribution the academic autopsy makes in complementing and improving clinical practice remains imperative.