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Updated: Jun 2, 2026

Direct Re-implantation of Left Coronary Artery into the Aorta in Adults with Anomalous Origin of Left Coronary Artery from the Pulmonary Artery (ALCAPA)

Direct Re-implantation of Left Coronary Artery into the Aorta in Adults with Anomalous Origin of Left Coronary Artery from the Pulmonary Artery (ALCAPA)

Published on: April 24, 2017

Left atrial angiosarcoma: an unusual presentation and location.

Saqib Masroor¹, Rammohan Marla

¹Division of Cardiothoracic Surgery, Medical College of Wisconsin, 9200 West Wisconsin Avenue, Milwaukee, WI 53226, USA. Smasroor@mcw.edu

The Journal of Heart Valve Disease

|May 13, 2011

Summary

Primary cardiac angiosarcoma is a rare, aggressive tumor. This case highlights a left atrial angiosarcoma causing severe dyspnea, rapid recurrence after surgery, and poor prognosis, emphasizing the need for early detection and effective treatment strategies.

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Area of Science:

Cardiology
Oncology
Pathology

Background:

Primary cardiac sarcomas are aggressive neoplasms.
These tumors show a predilection for the right side of the heart.

Observation:

A case of a highly aggressive angiosarcoma involving the entire left atrium is presented.
The patient experienced a rapidly progressive history of dyspnea.

Findings:

Surgical resection revealed invasion into the left pulmonary veins.
The patient suffered a recurrence within three months of surgery.
The patient died one year after initial presentation.

Implications:

This case underscores the aggressive nature and poor prognosis of left atrial angiosarcoma.

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Last Updated: Jun 2, 2026

Direct Re-implantation of Left Coronary Artery into the Aorta in Adults with Anomalous Origin of Left Coronary Artery from the Pulmonary Artery (ALCAPA)

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Published on: April 24, 2017

Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques

Cardiac Magnetic Resonance for the Evaluation of Suspected Cardiac Thrombus: Conventional and Emerging Techniques

Published on: June 11, 2019

Early diagnosis and effective therapeutic strategies are crucial for improving patient outcomes.

Further research into the management of primary cardiac sarcomas is warranted.