twitter
en POLSKI
eISSN: 2719-3209
ISSN: 0023-2157
Klinika Oczna / Acta Ophthalmologica Polonica
Current issue Archive Videos Articles in press About the journal Supplements Editorial board Reviewers Abstracting and indexing Subscription Contact Instructions for authors Publication charge Ethical standards and procedures
Editorial System
Submit your Manuscript
SCImago Journal & Country Rank
3/2019
vol. 121
 
Share:
Share:
abstract:
Original paper

Treatment Modalities of Ocular Lesions in von Hippel-Lindau Syndrome

Maria Siedlińska
1
,
Agnieszka Kubicka-Trząska
1, 2
,
Krzysztof Morawski
1
,
Bożena Romanowska-Dixon
1, 2

  1. Oddział Kliniczny Kliniki Okulistyki i Onkologii Okulistycznej Szpitala Uniwersyteckiego w Krakowie
  2. Katedra Okulistyki Uniwersytetu Jagiellońskiego Collegium Medicum
Online publish date: 2019/11/18
View full text Get citation
 
PlumX metrics:
Introduction
Von Hippel-Lindau (vH-L) syndrome is a rare autosomal dominant inherited disease, in which mutation of the VHL gene leads to formation of tumors in various different parts of the body, as well as hemangioblastomas in the retina.

Purpose
The aim of the study is to present the various methods of treatment of retinal hemangioblastomas associated with vH-L syndrome and the results of these therapies, their effects on anatomical status as well as the function of the treated eyes.

Material and methods
Twelve patients (18 eyes) with retinal hemangionblastomas were treated in years 1990-2015 in Ophthalmology and Ocular Oncology Clinic in Cracow.The following therapies were applied: laserocoagulation, cryoaplication, pars plana vitrectomy (ppV), transpupillary thermotherapy, photodynamic therapy, brachytherapy and intravitreal injections of anti-VEGF.

Results
Among our patients in 11 cases (16 eyes) multiple treatment modalities were performed, one eye underwent only laserocoagulation and one patient (one eye) underwent only cryoaplication of a single retinal hemangioblastoma. Another patient, after insufficient cryoaplication and TTT, underwent additional 106Ru brachytherapy. Despite of multiple therapies, five patients developed tractional and/or rhegmatogenous retinal detachment and pars plana vitrectomy with silicone oil endotamponade was performed. In one eye after application of intravitreal injections of anti-VEGF factor, the additional therapy, including TTT, cryotherapy, laserocagulation and ppV were performed. In a follow-up period in spite of application of many different and complementary treatments, the progression of ocular lesions and development of serious local complications were observed.

Conclusions
Our results show that treatment efficacy of vH-L hemangiomas is uncertain and depends on localization, number, size of the retinal lesions and dynamics of the disease. The development of posttreatment complications, deteriorate the prognosis of the visual acuity of the treated eye.

keywords:

Hippel-Lindau syndrome, haemangioblastoma of the retina, retinal detachment

Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.