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一名患有发育性青光眼和静脉曲张的年轻男性的双侧色素血管性母斑病

Bilateral Phacomatosis Pigmentovascularis in a Young Male with Developmental Glaucoma and Varicose Veins.

作者信息

Singh Kirti, Dangda Sonal, Mutreja Ankush, Bhattacharyya Mainak, Jaisingh Kirti

机构信息

Director Professor, Guru Nanak Eye Centre, Maulana Azad Medical College, New Delhi, India.

Research Fellow, New York Eye and Ear Infirmary, New York, USA (Formerly Senior Resident, Guru Nanak Eye Centre, Maulana Azad Medical College, New Delhi, India).

出版信息

J Curr Glaucoma Pract. 2018 May-Aug;12(2):94-98. doi: 10.5005/jp-journals-10008-1251. Epub 2018 Aug 1.

Abstract

AIM

To 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.

BACKGROUND

The 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 DESCRIPTION

A 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.

CONCLUSION

This 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 SIGNIFICANCE

This 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. 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.

摘要

目的

报告一例年轻男性双侧色素血管性母斑病(PPV),伴有发育性青光眼和高度近视以及克-特-韦综合征(KTW)的全身特征。

背景

眼皮肤黑素细胞增多症(ODM)和葡萄酒色斑并存被太田称为PPV。葡萄酒色斑是斯特奇-韦伯综合征(SWS)的一部分。KTW表现为静脉曲张和组织肥大以及葡萄酒色斑。

病例描述

一名22岁男性因高度近视和晚期青光眼导致视力下降。偶然发现有色素痣以及面部葡萄酒色斑,这些共同构成了PPV。还发现双侧静脉曲张,这通常与KTW相关。鉴于晚期视野损害以及局部用药无法控制眼压(IOP),他接受了双眼青光眼滤过手术。术中采取措施避免通过控制性前房穿刺突然减压,并采用可松解缝线进行巩膜瓣关闭,以防止术后早期出现低眼压相关并发症。这些预防措施使术后恢复顺利,即使在3年的随访中,患者眼压维持在十几岁的水平,视力和视野稳定。

结论

本病例突出了先天性疾病如眼皮肤黑素囊肿(ODM)、SWS、KTW的重叠特征,出现在一名年轻男性身上。PPV较少报道的全身特征包括腭部色素沉着和腭部血管畸形。

临床意义

本病例再次强调了这些实体PPV和KTW起源于神经嵴细胞。早期识别全身特征并在适当预防措施下及时进行手术干预,在这种发育性青光眼病例中可挽救视力。辛格K、丹达S、穆特雷贾A、巴塔查里亚M、贾辛格K。一名患有发育性青光眼和静脉曲张的年轻男性双侧色素血管性母斑病。《当代青光眼实践杂志》2018年;12(2):94 - 98。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01dd/6236123/9baa860dacaa/jocgp-12-094-g001.jpg

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