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Published on: May 16, 2020
Dilated Cardiomyopathy Caused by Wilms Tumor
Emmanuelle Chalavon1, Marie-Emilie Lampin, Cyril Lervat
1From the *Pediatric Oncology Unit, Lille Anti Cancer Center Oscar Lambret; †Intensive Care Unit, Lille Children's Hospital, ‡Department of Pathology, Lille University Hospital §Department of Surgery, Lille Children's Hospital, and ║Department of Cardiology, Lille University Hospital, Lille, France.
A rare case of a 7-month-old girl with unilateral Wilms tumor (a type of kidney cancer) and dilated cardiomyopathy (heart muscle disease) is presented. Treatment improved both the tumor and cardiac function, highlighting a unique association.
Area of Science:
- Pediatric Oncology
- Pediatric Cardiology
- Cardio-oncology
Background:
- Wilms tumor is the most common pediatric kidney cancer.
- Dilated cardiomyopathy can lead to heart failure in children.
- The co-occurrence of these conditions is exceptionally rare, particularly without hypertension.
Observation:
- A 7-month-old infant presented with unilateral Wilms tumor and concurrent dilated cardiomyopathy.
- The patient experienced cardiac failure necessitating intensive care.
- No history of hypertension was noted in this case.
Findings:
- The patient received chemotherapy and underwent surgical tumor removal.
- Following treatment, significant improvement in cardiac function was observed.
- This case underscores a rare, non-hypertensive association between nephroblastoma and dilated cardiomyopathy.
Implications:
- Early recognition of cardiac issues in pediatric kidney cancer patients is crucial.
- This case expands the understanding of potential comorbidities in Wilms tumor.
- Further research into the pathophysiology linking nephroblastoma and cardiomyopathy is warranted.
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