10.6084/m9.figshare.7546706.v1 Imle R. Imle R. Tosev G. Tosev G. Behnisch W. Behnisch W. Schenk J.-P. Schenk J.-P. Rauch H. Rauch H. Mueller A. Mueller A. Gorenflo M. Gorenflo M. Loukanov T. Loukanov T. Kulozik A. Kulozik A. Nyarangi-Dix J. Nyarangi-Dix J. Supplementary Material for: Intracardiac Extension of Wilms Tumor: A Case of a 2.5-Year-Old Girl Presenting with Upper Venous Congestion Caused by Tumor Growth into the Right Cardiac Ventricle Karger Publishers 2019 Wilms Tumor Intravascular tumor extent Intracardiac tumor extent Cardiopulmonary bypass Neoadjuvant chemotherapy 2019-01-04 10:44:26 Dataset https://karger.figshare.com/articles/dataset/Supplementary_Material_for_Intracardiac_Extension_of_Wilms_Tumor_A_Case_of_a_2_5-Year-Old_Girl_Presenting_with_Upper_Venous_Congestion_Caused_by_Tumor_Growth_into_the_Right_Cardiac_Ventricle/7546706 While Wilms tumors (WT) typically present solely with an abdominally palpable mass, rare cases exhibiting vascular tumor growth can also present with circulatory problems. Here, we report the case of a 2.5-year-old girl presenting with upper venous congestion and arterial hypertension as the primary symptoms of intraventricular tumor growth exhibiting remarkable tubular and perfused morphology. Clinical situation stabilized after initiation of neoadjuvant chemotherapy (NAC) with actinomycin D and vincristine, followed by surgical resection via laparotomy and sternotomy supported by cardiopulmonary bypass and deep hypothermia. Our results highlight the previously reported feasibility of this approach, even in primarily unstable patients.