Previous Page  15 / 32 Next Page
Information
Show Menu
Previous Page 15 / 32 Next Page
Page Background

Notes:

Page 35

Ophthalmology Congress 2016

December 05-06, 2016

Volume 7 Issue 11(Suppl)

J Clin Exp Ophthalmol

ISSN: 2155-9570 JCEO, an open access journal

conferenceseries

.com

December 05-06, 2016 Madrid, Spain

7

th

European Ophthalmology Congress

Malik Y Ghannam et al., J Clin Exp Ophthalmol 2016, 7:11(Suppl)

http://dx.doi.org/10.4172/2155-9570.C1.054

Acute multifocal hemorrhagic retinal vasculitis in a child: A case report

Malik Y Ghannam

1

, Mohammed Naseemuddin

2

, Peter Weiser

2

and John O Mason

2

1

An-Najah National University, Palestine

2

University of Alabama, USA

Background:

Acute multifocal hemorrhagic retinal vasculitis (AMHRV) is a rare disease with unknown incidence that

presents with abrupt onset of visual loss associated with retinal vasculitis, retinal hemorrhage, non-confluent posterior retinal

infiltrates, vitreous cellular inflammation and papillitis in, otherwise, healthy adult individuals. The reported treatment options

for acute multifocal hemorrhagic retinal vasculitis are oral corticosteroids, intravitreal ganciclovir and laser photocoagulation

or vitrectomy. We report a child with acute multifocal hemorrhagic retinal vasculitis who was treated with aggressive

immunosuppressive therapy resulting in a favorable visual outcome.

Case Presentation:

This is a retrospective case report of a 10-year-old African American girl who developed unilateral

acute multifocal hemorrhagic retinal vasculitis, which later on progressed bilaterally. We conducted a review of the clinical,

laboratory and photographic records to evaluate her functional and anatomic outcome after aggressive immunosuppressive

treatment. During the first four months of treatment of OD with intravitreal ganciclovir, intravitreal dexamethasone and

systemic prednisone, the change in vision in OD improved from light perception (LP) to counting fingers (CF). During the

next 18 months of aggressive systemic treatment of OD and the newly affected left eye (OS), the change in vision improved

from CF in OD and CF in OS to 20/200 in OD and 20/80 in OS. Management during the 18-month interval included rituximab

infusions, cyclophosphamide/methylprednisolone infusions, prednisone and mycophenolate.

Conclusions:

This is the first reported case of acute multifocal hemorrhagic retinal vasculitis occurring in a child.

Ophthalmologists should be aware of the need to treat severe acute multifocal hemorrhagic retinal vasculitis with aggressive

immunosuppressive agents in collaboration with rheumatologists to obtain the best possible visual outcome.

Biography

Dana Ghazaleh is currently a Medical student at An-Najah National University, Palestine. Her passion for medicine has come to surface ever since high school where

she founded a weekly medical show in the school broadcast to promote health and wellness among the community. She has been part of many voluntary projects

which fostered her desire more and more in pursuing her career as a physician. During college years, she expressed great interest in providing competent and

compassionate care for a wide variety of patients. Moreover, she realized the role of scientific research as a major contributor to medical care development, so she

became a Research Assistant. She was the Student Representative for a whole of 4 years. Her professional interests include internal medicine and ophthalmology.

danaghazaleh@hotmail.com