Rhabdoid tumors are rare but highly aggressive malignancies of infancy and early childhood with a generally unfavorable prognosis. Despite a wide variety of anatomic locations rhabdoid tumors share mutational inactivation of the SWI/SNF (SWItch/Sucrose NonFermentable) core component gene SMARCB1 (also known as INI1, hSNF5 or BAF47) in chromosome 22. As this inactivation usually results in loss of SMARCB1 expression, detectable by an antibody against the SMARCB1 protein, the accurate diagnosis of a rhabdoid tumor may be more distinctly and frequently made. Several reports on rhabdoid tumors presenting in various anatomic sites outside the kidneys and CNS are on record. We report two cases of rhabdoid tumors originating in the heart (cardiac tissue), which were entered into the European Rhabdoid Registry (EU-RHAB). The first case presented with intracardial and -cranial lesions as well as malignant ascites, while the second patient demonstrated an isolated cardiac tumor. This induced a different therapeutic approach and subsequently different clinical course (death 7 weeks after diagnosis in patient 1). Patient 2 presented with a bifocal intracardial tumor without metastases and remains in complete remission for 46 months since diagnosis following multimodal therapy. The second case demonstrates that even in a potentially futile clinical situation early and accurate diagnosis followed by prompt and intensive multimodal therapy may offer prolonged survival, potential cure and improved quality of life.

Children's Hospital Augsburg Swabian Children's Cancer Center Augsburg Germany

Children's Hospital Augsburg Swabian Children's Cancer Center Augsburg Germany; Department of Pediatric Hematology and Oncology University Children's Hospital Münster Germany

Department of Biology and Medical Genetics University Hospital Motol Charles University 2nd Medical School Prague Czech Republic

Department of Paediatric Haematology and Oncology University Medical Center Hamburg Eppendorf Germany

Department of Pathology and Molecular Medicine University Hospital Motol Charles University 2nd Medical School Prague Czech Republic

Department of Pediatric Hematology and Oncology Childrens' Hospital Schwabing University of Technology Munich Germany

Department of Pediatric Hematology and Oncology University Hospital Motol Charles University 2nd Medical School Prague Czech Republic

Department of Radiology University of the Saarland Homburg Saar Germany

Institute of Human Genetics Christian Albrechts University Kiel and University Hospital Schleswig Holstein Campus Kiel Kiel Germany

Kardiocentrum and Cardiovascular Research Centre University Hospital Motol Prague Czech Republic

Kiel Pediatric Tumor Registry Department of Pediatric Pathology University Kiel Germany

References provided by Crossref.org

Age and DNA methylation subgroup as potential independent risk factors for treatment stratification in children with atypical teratoid/rhabdoid tumors