Journal of Pediatric Surgery
Volume 43, Issue 5 , Pages e27-e29, May 2008

Congenital mesoblastic nephroma rich from mitosis after in vitro fertilization: a case report

Department of Pediatric Surgery, Faculty of Medicine, Baskent University, 06490 Bahçelievler, Ankara, Turkey

Received 9 October 2007; received in revised form 3 January 2008; accepted 4 January 2008.

Abstract 

Recently, various childhood tumors such as leukemia, neuroblastoma, hepatoblastoma, retinoblastoma, and central nervous system tumors in patients born after assisted conception have been reported. Although involvement of in vitro fertilization in the tumor pathogenesis was not established, the likely effect of assisted reproductive technology has been increasingly considered in these tumors in the last decade. Congenital mesoblastic nephroma is the most common renal tumor of infancy younger than 6 months associated with an overall good prognosis. The cellular variant of congenital mesoblastic nephroma, which occurs primarily in infants older than 3 months, confers a less favorable prognosis. We present a case of an atypical congenital mesoblastic nephroma with cellular elements in a 2-month-old infant who was born after in vitro fertilization. To our knowledge, this is the second congenital mesoblastic nephroma case and the first one with cellular variant reported to date in the English literature after a pregnancy induced by an assisted reproductive technology.

Key words: Congenital mesoblastic nephroma, Neonatal tumor, In vitro fertilization, Assisted reproduction technology, Retinoblastoma

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PII: S0022-3468(08)00016-X

doi:10.1016/j.jpedsurg.2008.01.008

Journal of Pediatric Surgery
Volume 43, Issue 5 , Pages e27-e29, May 2008