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.