Wilms tumor, pleuropulmonary blastoma, and DICER1: case report and literature review
Olivier Abbo1, Kalitha Pinnagoda2, Laurent Brouchet3
1Pediatric Surgery Department, Children's Hospital of Toulouse, CHU Toulouse, 330 Avenue de Grande Bretagne, 31059, Toulouse, France. abbo.o@chu-toulouse.fr.
Background:
Pleuroblastoma (PPB) is a rare pediatric tumor which, in 30% of cases, is associated with cystic nephroma. It has been recently linked to the DICER1 mutation as part of a predisposition syndrome for various tumors. However, if DICER 1 anomalies have been reported in patients with Wilms tumor (WT), to date, no cases of PPB, WT, and DICER1 mutations have been reported in the same patient.
Case Presentation:
We report the case of a 3-year-old patient, initially managed for metastatic WT. During his clinical course, the diagnosis of a PPB was made after detecting the DICER1 mutation and subsequent management was therefore modified.
Conclusion:
This case highlights that in case of simultaneous discovery of a renal tumor and a pulmonary lesion in a child, the DICER 1 mutations should be looked for as these could help adapt management and schedule the surgical procedures.
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