|
- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2014
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/18063
Title: | Ocular complications in patients with Marfan syndrome - considerations on two clinical cases |
Authors: | Pavlovschi, Ecaterina Lîsîi, Irina |
Keywords: | Marfan syndrome;ocular manifestations;lens subluxation;surgical treatment |
Issue Date: | 2014 |
Publisher: | Ministry of Health of the Republic of Moldova, State Medical and Pharmaceutical University Nicolae Testemitanu, Medical Students and Residents Association |
Citation: | PAVLOVSCHI, Ecaterina, LÎSÎI, Irina. Ocular complications in patients with Marfan syndrome - considerations on two clinical cases. In: MedEspera: the 5th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2014, pp. 185-186. |
Abstract: | Introduction: Marfan syndrome is an autosomal dominant connective tissue disorder due to
mutations in the fibrillin 1 gene (15 q21.1). Ocular features are highly variable and may be
complicated by blindness. Ectopia lentis (subluxation of lens) is a hallmark feature of Marfan
syndrome (according to international Ghent criteria) and is present in approximately 60% to 80% of
patients; in most cases it is found until the age of 10.
Materials and methods: The authors present two clinical cases of 2 children with
predetermined Marfan syndrome with bilateral ectopia lentis, admitted to the Medical Center
Ophthalmology "Ovisus".
Results: In the 1st case both eyes underwent extracapsular lens extraction by phacoaspiration with a scleral fixated capsular tension ring (right eye) and a non-sutured capsular tension ring (left
eye) and primary implantation of lOL (26,OD for RE and 27,OD for LE, AcrySof IQ) in the capsular
bag. In the 2nd case, the bilateral lens dislocation was treated by lensectomy with primary
implantation of scleral fixation IOL (18,0D for the right eye, 24,0 D for the left eye).
Discussion: Ophthalmologists play an important role in detecting Marfan syndrome. The
diagnosis and management of the many associated ocular disorders is challenging. Patients should be
instructed to seek immediate ophthalmological consultation if light flashes, floaters or any sudden
decrease of vision occur. Timely diagnosis and treatment of refractive problems, retinal detachment and
glaucoma can prevent amblyopia and help to preserve sight in patients with this syndrome.
Conclusions: Management of ocular complications in Marfan syndrome must be
multidisciplinary and include a treatment plan tailored to each individual’s manifestations. Due to
zonular reliability and resulting capsular instability, the correction of the aphakia with intraocular lens
implantation in lens subluxation is a challenge. In some cases, subluxation can be compensated by
optical correction, but this does not prevent other complications. Surgery, though difficult, provides an
improved, stable visual acuity, preventing amblyopia (in children). At the moment, one of the methods
of choice is extraction of subluxated lens with capsular ring placement (with or without scleral fixation)
and primary implantation of the IOL in the capsular bag. Eye control is performed annually and assesses
intraocular pressure, peripheral retina, the optic nerve and refractive disorders. |
metadata.dc.relation.ispartof: | MedEspera: The 5th International Medical Congress for Students and Young Doctors, May 14-17, 2014, Chisinau, Republic of Moldova |
URI: | http://repository.usmf.md/handle/20.500.12710/18063 |
Appears in Collections: | MedEspera 2014
|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
|