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dc.contributor.authorDurmus, Gul
dc.contributor.authorBoybeyi-Turer, Ozlem
dc.contributor.authorGharibzadeh-Hizal, Mina
dc.contributor.authorEkinci, Saniye
dc.contributor.authorKiper, Nural
dc.date.accessioned2019-12-12T06:43:00Z
dc.date.available2019-12-12T06:43:00Z
dc.date.issued2018
dc.identifier.issn0041-4301
dc.identifier.urihttps://doi.org/10.24953/turkjped.2018.05.025
dc.identifier.urihttp://hdl.handle.net/11655/16777
dc.description.abstractMeconium periorchitis (MPO) is a rare disorder caused by meconium peritonitis with the leakage of meconium into the scrotal sac through the patent processus vaginalis. MPO may be rarely detected during inguinal hernia repair. The association of MPO with cystic fibrosis is rarely seen. We present a male infant with the complaint of left groin swelling, compatible with reducible inguinal hernia. An herniotomy was carried out and the greenish nodules with calcifications were detected. Histopathological examination was compatible with MPO. Two months later the patient was diagnosed with atypical cystic fibrosis. Clinicians should be aware of MPO presentations and its appearance on the hernia sac to prevent unnecessary orchiectomy.
dc.language.isoen
dc.publisherTurkish J Pediatrics
dc.relation.isversionof10.24953/turkjped.2018.05.025
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPediatrics
dc.titleMeconium Periorchitis: An Incidentally Diagnosed Rare Entity During Inguinal Herniorraphy
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalTurkish Journal Of Pediatrics
dc.contributor.departmentÇocuk Cerrahisi
dc.identifier.volume60
dc.identifier.issue5
dc.identifier.startpage612
dc.identifier.endpage614
dc.description.indexWoS
dc.description.indexScopus


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