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Published on: April 4, 2011
Meconium periorchitis: An incidentally diagnosed rare entity during inguinal herniorraphy
Gül Durmuş1, Özlem Boybeyi-Türer1, Mina Gharibzadeh-Hizal2
1Department of Pediatric Surgery, Hacettepe University, Faculty of Medicine, Ankara, Turkey.
Abstract:
Durmuş G, Boybeyi-Türer Ö, Gharibzadeh-Hizal M, Ekinci S, Kiper N. Meconium periorchitis: An incidentally diagnosed rare entity during inguinal herniorraphy. Turk J Pediatr 2018; 60: 612-614. Meconium 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.
Insights
Meconium periorchitis (MPO) is a rare condition where meconium leaks into the scrotum. It can be incidentally found during inguinal hernia repair, sometimes preceding a cystic fibrosis diagnosis.
Area of Science:
- Pediatric Surgery
- Neonatal Pathology
- Gastroenterology
Background:
- Meconium periorchitis (MPO) is a rare disorder resulting from meconium peritonitis, with meconium entering the scrotal sac via a patent processus vaginalis.
- MPO is infrequently diagnosed during surgical repair of inguinal hernias.
Observation:
- A male infant presented with left groin swelling, indicative of a reducible inguinal hernia.
- During herniotomy, greenish nodules with calcifications were observed within the hernia sac.
- Histopathological examination confirmed Meconium periorchitis (MPO).
Findings:
- The infant was diagnosed with atypical cystic fibrosis two months post-operatively.
- This case highlights the association between MPO and cystic fibrosis, although rare.
Implications:
- Clinicians should recognize MPO's presentation during inguinal hernia repair to avoid misdiagnosis or unnecessary procedures like orchiectomy.
- Awareness of MPO's potential association with cystic fibrosis is crucial for timely diagnosis and management.
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