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A Case of Refractory Childhood Glaucoma Associated With Sturge-Weber Syndrome Treated With Baerveldt Glaucoma Implant
Wakako Imamura1, Akira Matsuda1, Akira Hirota1
1Division of Ophthalmology, Nihon University School of Medicine, Tokyo, Japan, nihon-u.ac.jp.
Insights
This case study details treating refractory childhood glaucoma in a Sturge-Weber syndrome (SWS) patient with a Baerveldt glaucoma implant (BGI). Careful management is crucial to avoid complications like retinal detachment post-surgery.
Area of Science:
- Ophthalmology
- Pediatric Glaucoma Management
- Vascular Anomalies
Background:
- Sturge-Weber syndrome (SWS) can cause refractory childhood glaucoma.
- Previous surgeries included trabeculotomies and vitrectomy for complications.
- The patient presented with severe intraocular pressure (30 mmHg) despite maximal medical therapy.
Purpose of the Study:
- To report the clinical course of refractory childhood glaucoma in a patient with SWS.
- To evaluate the use of Baerveldt glaucoma implant (BGI) in this complex case.
- To highlight potential complications and management strategies.
Main Methods:
- A 14-year-old male with SWS received a Baerveldt glaucoma implant (BGI).
- Conservative management was initiated for postoperative complications.
- Intraocular pressure was monitored closely.
Main Results:
- The patient developed extensive serous retinal and choroidal detachments on postoperative day 9.
- These detachments resolved within 8 days with conservative therapy.
- The complication was potentially linked to SWS-related choroidal hemangioma and episcleral venous pressure.
Conclusions:
- Baerveldt glaucoma implant (BGI) can be used for refractory childhood glaucoma in SWS.
- Close monitoring for complications like serous detachments is essential.
- Avoiding postoperative hypotony is critical in managing secondary childhood glaucoma associated with SWS.
Abstract:
We reported the clinical course of refractory childhood glaucoma associated with Sturge-Weber syndrome (SWS) treated with Baerveldt glaucoma implant (BGI). The patient was a 14-year-old male diagnosed with SWS after birth. He had previously undergone four trabeculotomies for glaucoma and vitrectomy for submacular hemorrhage from a diffuse choroidal hemangioma in his left eye. Before the BGI surgery, his intraocular pressure was 30 mmHg under full medications. The patient experienced extensive serous retinal and choroidal detachments on Postoperative Day 9. The cause may have been the increased leakage of serous fluid from the choroidal hemangioma and the high venous pressure in the episclera due to SWS. Retinal and choroidal detachments subsided within 8 days with conservative therapy. It is important to avoid postoperative hypotony for the treatment of secondary childhood glaucoma due to SWS.
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