| Literature DB >> 26388605 |
Oktav Bosnalı1, İnanç Cici, Serdar Moralıoğlu, Ayşenur Cerrah-Celayir.
Abstract
Splenogonadal fusion is a rare congenital anomaly. It has two subtypes, discontinuous and continuous. Up to one-third of continuous-type fusion is associated with other congenital anomalies. We present a continuous-type splenogonadal fusion case that was found incidentally during indirect hernia repair; the testicle was preserved during excision. Laparoscopic exploration was helpful in identifying the isolated polysplenia as the origin of continuous-type splenogonadal fusion, and in excising the cord-like attachment proximally. The patient had no other associated anomaly.Entities:
Mesh:
Year: 2014 PMID: 26388605
Source DB: PubMed Journal: Turk J Pediatr ISSN: 0041-4301 Impact factor: 0.552