Persistent primary vitreous: A report on 2 rare pediatric cases
Persistence of the fetal vasculature (PFV) is a rare ocular malformation of unknown origin, characterized by a spectrum of complex presentations with varying functional prognoses. We reported the cases of 2 male patients: a 3-month-old infant and a 4-year-old child. A thorough examination of their eyes, often requiring general anesthesia, is essential for diagnosis. The malformation can manifest in mild forms without visual impact or associated anomalies, as well as severe forms involving multiple ocular structures and systemic syndromes. A comprehensive pediatric examination is recommended to identify any associated conditions. Treatment is personalized and typically includes early, targeted surgical and medical interventions to optimize outcomes. The cases highlight the importance of early diagnosis and comprehensive evaluation in managing persistence of the fetal vasculature, as timely intervention can significantly improve visual outcomes.
Authors
- Sanae Jellal
- Jihane El Houssni (ORCID: https://orcid.org/0000-0002-9738-341X)
- Fatima Zohra Benbrahim (ORCID: https://orcid.org/0009-0009-8517-9524)
- Latifa Chat (ORCID: https://orcid.org/0000-0002-6902-1913)
- Rachida Chehrastane
- Sara Ez-Zaky
- Siham El Haddad
- Nazik Allali
Institutions
- Hôpital Ibn Sina-Rabat (MA)
- Ibn Sina Hospital (KW)
Publication Details
- Journal
- Radiology Case Reports
- Published
- 2024-10-31
- DOI
- https://doi.org/10.1016/j.radcr.2024.10.045
- Citations
- 1
- Primary Topic
- Retinal and Macular Surgery
- Type
- article
- Field-Weighted Citation Impact
- 0.40