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Research Article Open access CC BY 4.0

A Rare Case of Chiai II Malformation with Uterine Rupture at a Regional Hospital in Guyana

Kudzai Sengwe, Cosmos Ikpefuran

International Journal of Research and Reports in Gynaecology · pp. 417–423 · Published 16 Oct 2026

10.9734/ijrrgy/2026/v9i1192

Abstract

Background: Chiari II malformation is a congenital hindbrain anomaly that is commonly associated with neural tube defects and can present substantial prenatal and perinatal management challenges. This report describes an unusual co-occurrence of Chiari II malformation and rupture of an unscarred uterus. Case Presentation: A 26-year-old woman, G3P2001, was admitted at 40 weeks + 6 days of gestation for delivery. She had attended 10 antenatal visits and had undergone one ultrasound examination at 17+0 weeks, which reported no congenital abnormality. She presented in spontaneous labour at 5 cm cervical dilatation with spontaneous rupture of membranes and a breech presentation. Emergency caesarean delivery resulted in the birth of a live male neonate weighing 5.3 kg, with Apgar scores of 2 and 2. The neonate had hydrocephalus, clubfoot, spina bifida, and meningiomylocele. Intraoperative examination identified an 8 cm rupture of the unscarred uterus extending from the lower segment to the fundus. Hysterorrhaphy and B-Lynch compression sutures achieved haemostasis; estimated blood loss was 450 mL. The neonate died after 100 minutes. Post-mortem findings included cerebral atrophy, congenital hydrocephaly consistent with Arnold-Chiari type II malformation, and meningiomylocele. Conclusion: This case highlights the importance of accurate prenatal detection, counselling, multidisciplinary planning, and prompt obstetric management when severe fetal anomalies and unexpected maternal complications occur.

Chiari II malformation hydrocephalus meningiomylocele spina bifida neural tube defects uterine rupture

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