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Updated: Jul 27, 2025

Chronic Thromboembolic Pulmonary Hypertension and Assessment of Right Ventricular Function in the Piglet
Published on: November 4, 2015
Case report: obstruction in the right ventricular outflow tract due to hemolymphangioma
Bo Chen1, Ting Fan1, Yong Cao1
1Department of Cardiovascular Surgery, GaoZhou People's Hospital, Gaozhou, China.
Insights
A rare hemolymphangioma, a congenital vascular malformation, was found in the right ventricular outflow tract. This cardiac tumor was successfully removed, with no recurrence observed after 18 months.
Area of Science:
- Cardiology
- Vascular Malformations
- Surgical Oncology
Background:
- Cardiac masses include primary tumors, metastatic diseases, and endocarditis, with myxomas being the most common primary cardiac tumor (75%).
- Hemolymphangiomas are congenital mesenchyme-derived vascular and lymphatic malformations with an incidence of 0.12%-0.28% annually.
- While found in various organs, hemolymphangiomas have not been previously reported in the heart's ventricular outflow tract.
Observation:
- This report details a case of a hemolymphangioma located in the right ventricular outflow tract (RVOT).
Findings:
- The hemolymphangioma in the RVOT was surgically resected.
- Post-operative follow-up for 18 months showed no evidence of tumor recurrence.
Implications:
- This case expands the known anatomical locations for hemolymphangiomas.
- Successful surgical management of RVOT hemolymphangioma demonstrates a viable treatment option.
- Highlights the importance of considering rare vascular malformations in cardiac mass differential diagnoses.
Abstract:
Cardiac masses commonly involve primary tumors, metastatic diseases, and nonbacterial thrombotic and infective endocarditis. myxomas are the most common primary tumors, accounting for 75%. Hemolymphangiomas are a group of congenital vascular and lymphatic malformations that originate from the mesenchyme, with an incidence rate of 0.12%-0.28% per year. Hemolymphangiomas have been found in the rectum, small intestine, spleen, liver, chest wall, and mediastinum but have not yet been reported in the ventricular outflow tract in the heart. Herein, we report a case of a hemolymphangioma tumor in the right ventricular outflow tract (RVOT). The tumor was successfully resected, and the patient was followed up for 18 months and did not exhibit tumor recurrence.
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