Uncommon Presentation of Wyburn-Mason Syndrome in a Pediatric Patient

Authors

  • Julie Barliana
  • Syntia Nusanti
  • Manoa Panjaitan
  • Anggun Yudantha
  • Laura Djunaedi

DOI:

https://doi.org/10.35749/journal.v47i1.100146

Keywords:

Arteriovenous Malformation, Racemose hemangiomatosis, Wyburn-Mason syndrome

Abstract

We report an uncommon presentation of Wyburn-Mason syndrome in a pediatric patient. An 11-year- old girl presenting with no light perception in her right eye. Examination revealed an exotropia and a large and tortuous retina vessel in the posterior part of her right eye. However, other examinations, including dermatological and neurological examination, are within normal limits. Magnetic Resonance Angiography (MRA) showed vascular malformation at the basal cistern that extends to the retrobulbar area. Therefore, a thorough examination of the eye and brain, including MRA, is mandatory in every case, even in pediatric with normal neurological examinations.

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References

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Pangtey BP, Kohli P, Ramasamy K. Wyburn– Mason syndrome presenting with bilateral ret- inal racemose hemangioma with unilateral se- rous retinal detachment. IJO 2018; 66:1869- 71

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Published

2021-02-25

How to Cite

Barliana, J., Nusanti, S., Panjaitan, M., Yudantha, A., & Djunaedi, L. (2021). Uncommon Presentation of Wyburn-Mason Syndrome in a Pediatric Patient. Ophthalmologica Indonesiana, 47(1), 20-23. https://doi.org/10.35749/journal.v47i1.100146

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