Hemangioendothelioma: A rare case of a primary intracardiac tumor

Andrea Beaton, Trevor Kuttler, Ali Hassan, Dilip S. Nath, Christine Reyes, Richard A. Jonas, Gerard R. Martin

Research output: Contribution to journalArticlepeer-review

4 Scopus citations


Kaposiform hemangioendothelioma (KH) is a rare tumor of vascular origin that commonly affects the cutaneous tissues of the extremities. It can, however, affect the abdomen, thorax, head, or neck. Compared with juvenile hemangiomas, which tend to regress, KH tumors are locally aggressive and usually persist. Associated morbidity and mortality rates range from 12 to 30 % and typically are related to either compressive effects on surrounding vital structures or effects of the Kasabach-Merritt phenomenon [10, 11, 13]. To our knowledge, this report is the first to describe KH presenting as a primary intracardiac tumor.

Original languageEnglish
Pages (from-to)194-197
Number of pages4
JournalPediatric Cardiology
Issue number1
StatePublished - Jan 1 2013


  • Cardiac tumor
  • Pediatric cardiology
  • Pericardial effusion


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