The scientific program is currently be created by the Meetings Committee, which consists of experts from various specialties across multiple continents. We also encourage you to consider participating in the meeting through the submission of a case. While we will not be able to include all submitted cases, we invite you to considering submitting some of your most interesting for inclusion.
Call for Cases
We are calling for cases and are asking for your most interesting, complicated, compelling, innovative and interdisciplinary dilemmas and controversies. For all cases that are submitted, we ask that they have a multidisciplinary approach (IR, Surgery, Medical) and you have information outlining how your team decided on the best approach for the case.
We are looking for the conundrums; cases that make our heads hurt; cases that, at first make sense, but something in our investigation did not fit (like a phenotype that did not go along with the genotype found); innovative therapeutic options; disorders that do not have an exact diagnosis, etc.
The cases, preferably, should fit in one of the following categories.
- Arteriovenous / venous / lymphatic / capillary malformations
- Complicated lymphatic anomalies (CLA: GLA / KLA / GSD /CCLA)
- Complicated hemangiomas
- Rare vascular tumors
- Cases that mimic vascular anomalies (but are not a vascular anomaly)
- Complications of medical treatment
Call for submissions closes on Friday, 09 December 2022 at 11:59 pm, US Eastern Time.
The program will be available after all cases have been received, reviewed and selected. We anticipate the program will be available in early 2023.