Abstract

ABSTRACTAimTo report a case of bilateral phacomatosis pigmentovascularis (PPV), in a young male,presenting with developmental glaucoma and high myopia along with systemic features of klippel trenanauy weber (KTW) syndrome.BackgroundThe co-existence of oculodermal melanocytosis (ODM)and port-wine stain was termed PPV by Ota. Port-wine stain presents as part of Sturge-Weber syndrome (SWS). KTW presents with varicose veins and tissue hypertrophy alongwith port-wine stain.Case DescriptionA 22-year-old male presented with decreased vision owing to high myopia and advanced glaucoma. Incidental findings noted were pigmentary naevi along with facial port-wine stain, which collectively comprises PPV. Also noted were bilateral varicose veins which are usually seen in association with KTW. In view of advanced visual field damage and inability to control intraocular pressures (IOP) on topical medications, he underwent Glaucoma filtration surgery in both eyes. Intra-operatively care was taken to avoid sudden decompression by controlled anterior chamber paracentesis, and scleral flap closure with releasable sutures was done to prevent hypotony related complications in the immediate postoperative period. Such precautions lead to an uneventful postoperative recovery, and even at 3 years’ follow-up, the patient is maintaining IOP in early teens along with a stable visual acuity and visual fields.ConclusionThis case highlights the overlapping features of congenital conditions like oculodermal melanocystosis (ODM), SWS, KTW; presenting in a young male. Systemic features reported less frequently with PPV, included palatal pigmentation and palatal vascular malformations.Clinical SignificanceThis case re-emphasizes a common origin of these entities, PPV and KTW, from the neural crest cells. Early recognition of the systemic features and timely surgical intervention under appropriate precautions, can be vision salvaging in such cases of developmental glaucoma.How to cite this article: Singh K, Dangda S, Mutreja A, Bhattacharyya M, Jaisingh K. Bilateral Phacomatosis Pigmentovascularis in a Young Male with Developmental Glaucoma and Varicose Veins. J Curr Glaucoma Pract 2018;12(2):94-98.

Highlights

  • The co-existence of oculodermal melanocytosis (ODM)and port-wine stain was termed phacomatosis pigmentovascularis (PPV) by Ota

  • Clinical Significance: This case re-emphasizes a common origin of these entities, PPV and klippel trenanauy weber (KTW), from the neural crest cells

  • Corresponding Author: Sonal Dangda, Research Fellow (Glaucoma), New York Eye and Ear Infirmary, New York, USA (Formerly Senior Resident, Guru Nanak Eye Centre, Maulana Azad Medical College, New Delhi, India), e-mail: sonaldangda@ gmail.com surgical intervention under appropriate precautions, can be vision salvaging in such cases of developmental glaucoma

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Summary

Introduction

The co-existence of oculodermal melanocytosis (ODM)and port-wine stain was termed PPV by Ota. Intra-operatively care was taken to avoid sudden decompression by controlled anterior chamber paracentesis, and scleral flap closure with releasable sutures was done to prevent hypotony related complications in the immediate postoperative period Such precautions lead to an uneventful postoperative recovery, and even at 3 years’ follow-up, the patient is maintaining IOP in early teens along with a stable visual acuity and visual fields. The condition is common in Asians and females, with bilateral cases being rare.[2] Glaucoma occurs in half of the patients with SWS and in 10% of those with ODM.[3,4] KTW, a separate entity, presents with an overlapping feature of port-wine stain along with varicose veins and tissue hypertrophy.[5,6]. We aim to highlight that early diagnosis and timely surgical intervention can prevent glaucoma blindness in these patients

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