A rare pediatric renal tumor: classic congenital mesoblastic nephroma: two cases and review of literature

Conclusion: When renal tumors occur in infancy or at neonatal age, mesoblastic nephroma should be kept in mind. Association of hypertension and paraneoplastic syndromes should be looked for. Surgery is usually curative and postoperative follow-up for recurrence is required, more so in cellular variety.
Source: Annals of Pediatric Surgery - Category: Surgery Tags: Original Articles Source Type: research