ArticleCase reports in oncology
Concurrent Wilms Tumor and Severe Dilated Cardiomyopathy in an Infant Requiring Veno-Arterial Extracorporeal Membrane Oxygenation.
Article in Case reports in oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
8 authors.
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Abstract
Introduction: The combination of Wilms tumor (WT) and severe dilated cardiomyopathy (DCM) in infants is a rare occurrence, as is the need for advanced life support with extracorporeal membrane oxygenation (ECMO). Case Presentation: We present a 3-month-old infant with concurrent WT and severe DCM, which required complex management, including urgent veno-arterial (VA) ECMO support and neoadjuvant chemotherapy prior to resection. Conclusion: This case underscores the exceptional nature of managing an infant with concurrent WT and DCM, highlighting the need for tailored, multidisciplinary approaches. The use of ECMO, neoadjuvant chemotherapy, and careful surgical planning facilitated the successful management of this complex pediatric patient.
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