ArticleItalian journal of pediatrics2023
Report and follow-up on two new patients with congenital mesoblastic nephroma.
Article in Italian journal of pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 4 citations in OpenAlex.
- Laparoscopic training in porcine models: a tool for continuous professional skill enhancement for paediatric surgeons.Pediatric surgery international · 2026Article
- Yolk sac tumor after post-detorsion changes in a torsed undescended testis: a case report.Translational andrology and urology · 2026Article
- Neonatal Esophageal Perforation: A Comprehensive Review of the Literature.Journal of clinical medicine · 2026Review
- Iatrogenic esophageal perforation in extremely preterm newborn with multiple comorbidities: case report and ethical considerations.Frontiers in pediatrics · 2026Article
- Testicular Torsion in Inguinal Cryptorchidism: Report on Two Patients and Literature Review.Children (Basel, Switzerland) · 2025Review
- Poor outcome in congenital mesoblastic nephroma withTranslational pediatrics · 2024Article
- A massive primary congenital mesoblastic nephroma was successfully managed through open total nephrectomy: a case report.Annals of medicine and surgery (2012) · 2023Article
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Authors and funding
10 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundTumors are rare in neonatal age. Congenital mesoblastic nephroma (CMN) is a usually benign renal tumor observed at birth, or in the first months of life. It may also be identified prenatally and associated with polyhydramnios leading to preterm delivery. Effective treatment is surgical in most cases, consisting in total nephrectomy. In literature, very few studies report on the neonatal management of such a rare disease, and even less are those describing its uncommon complications. CASES PRESENTATION: We report on two single-center newborns affected with CMN. The first patient is a preterm female baby, born at 30
conclusionsThe finding of a fetal abdominal mass should prompt suspicion of CMN, especially if it is associated with polyhydramnios; it should also alert obstetricians and neonatologists to the risk of preterm delivery. Although being a usually benign condition, CMN may be associated with neonatal systemic-metabolic or postoperative complications. High-level surgical expertise, careful neonatological intensive care and histopathological/cytogenetic-molecular definition are the cornerstones for the optimal management of patients. This should also include an individualized follow-up, oriented to the early detection of any possible recurrences or associated anomalies and to a better quality of life of children and their families.
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