Bilateral Glaucoma in a Rare Case of Overlapping Sturge-Weber Syndrome and Klippel-Trenaunay Syndrome

Author:

Chaudhuri Pallabi R.1,Biswas Uttam2,Dey Asim K.3,Chakraborty Milan4

Affiliation:

1. Department of Ophthalmology, B. N. Bose SD Hospital, Barrackpore, West Bengal, India

2. Department of Medicine, Burdwan Medical College and Hospital, Purba Burdwan West Bengal, India

3. Department of Ophthalmology, Gouri Devi Institute of Medical Sciences and Hospital, Durgapur, West Bengal, India

4. Department of Medicine, N. R. S. Medical College and Hospital, Kolkata, West Bengal, India

Abstract

We report a case of 6.year.old boy presented with dimness of vision having a past history of recurrent seizure for last four years and was found to have glaucoma in both eyes. He also had port.wine stain over both sides of face and hypertrophy of left hand and leg, venous prominence over abdominal wall and chest. CT scan shows left-sided angiomatosis in brain and venacaval anomalous connections in abdomen. This case reveals a very rare overlap between SWS and KTS presented with bilateral port-wine stain and bilateral glaucoma.

Publisher

Medknow

Reference8 articles.

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2. An infantile case of Sturge-Weber syndrome in association with Klippel-Trenaunay-Weber syndrome and phakomatosis pigmentovascularis;Lee;J Korean Med Sci,2005

3. Ophthalmic alterations in the Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and the phakomatosis pigmentovascularis: An independent group of conditions?;Abdolrahimzadeh;Biomed Res Int,2015

4. Syndrome de Klippel-Trenaunay avec colombe irien atypique;Schnyder;J Genet Hum,1956

5. Vascular malformations part II: Associated syndromes;Garzon;J Am Acad Dermatol,2007

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