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Section Endocrinology, Department of Medicine, Erasmus MC, Rotterdam, The Netherlands
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Introduction Over the past decades, survival rates of childhood nephroblastoma and neuroblastoma have increased to respectively ~90% and ~40–95% (strongly dependent on stadium) ( 1 , 2 ). These tumours are of embryonic origin, with a peak
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thyroidectomy. Struma nodosa and thyrotoxicosis occurred in seven patients, and hypothyerosis and type 2 diabetes mellitus occurred in three patients. One patient was previously subjected to unilateral nephrectomy due to the nephroblastoma. In three patients