Literature DB >> 27363968

Management of childhood glaucoma in Sturge Weber Syndrome: A challenge.

Poonam Lavaju, Pawan Mahat.   

Abstract

BACKGROUND: Sturge-Weber syndrome (SWS) is a rare congenital neuro- oculo- cutaneous disorder. Glaucoma is one of the ocular abnormalities associated with it. Management of glaucoma in SWS is challenging.
OBJECTIVE: To report surgical and visual outcome of trabeculectomy in bilateral glaucoma in Sturge-Weber syndrome and the challenges encountered in its management. CASE DESCRIPTION: A six-year-old girl presented with gradually progressive increase in size of both the eyes associated with watering, photophobia and diminution of vision since birth. On examination she was diagnosed to have bilateral SWS with glaucoma, refractive to antiglaucoma medications. She underwent trabeculectomy with intraoperative use of 5- FU. The post operative period was complicated with choroidal effusion in both the eyes with shallow anterior chamber. In the second post operative day, the right eye anterior chamber re- formation was done with ringer lactate solution. There was spontaneous resolution of choroidal effusion with normalization of intraocular pressure with no adverse effect on visual acuity within one week.
CONCLUSION: Treatment of glaucoma associated with Sturge-Weber syndrome is challenging. When planning surgical intervention an increased risk of choroidal effusion associated with it, should be kept in mind. © NEPjOPH.

Entities:  

Year:  2015        PMID: 27363968     DOI: 10.3126/nepjoph.v7i2.14979

Source DB:  PubMed          Journal:  Nepal J Ophthalmol        ISSN: 2072-6805


  2 in total

1.  Choroidal detachment with exudative retinal detachment following Ahmed valve implantation in Sturge-Weber syndrome.

Authors:  Bipul Kumer De Sarker; Ginger Helen; Mohammad Ibn Abdul Malek; Abdullahi Sadiq; Zafrul Hassan; Jahangir Kabir; Sarat Badmus; Iftekhar Sazzad; Mostafizur Rahman; Mallika Mahatma; Abdus Salam
Journal:  GMS Ophthalmol Cases       Date:  2019-10-25

Review 2.  Systemic and ocular manifestations of a patient with mosaic ARID1A-associated Coffin-Siris syndrome and review of select mosaic conditions with ophthalmic manifestations.

Authors:  Virginia Miraldi Utz; Diana S Brightman; Monica A Sandoval; Robert B Hufnagel; Howard M Saal
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-09-05       Impact factor: 3.359

  2 in total

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