Clinical experience in treatment of diffuse unilateral subretinal neuroretinitis

Purpose To describe the clinical features, management, and outcomes of patients with diffuse unilateral subacute neuroretinitis (DUSN). Methods A noncomparative, consecutive analysis of case series from two tertiary care campuses of LV Prasad Eye Institute, India, between January 2011 and April 2014 was performed. Medical records of the patients presenting with DUSN (early or late stage) were reviewed. Results The current study included 13 patients. The majority (10/13, 76.92%) of the patients were aged 20 years or less. All patients had unilateral eye involvement. Visual acuity at presentation was 20/200 or worse in 9/13 (69.23%) patients. A delay in diagnosis occurred in 6/13 patients, and initial diagnosis in these patients included retinitis pigmentosa (4 patients) and posterior uveitis (2 patients). Clinical features included early presentation (prominent vitritis, localized retinitis, and vasculitis) in 7/13 (53.85%) patients and late presentation (attenuation of vessels, retinal pigment epithelium atrophic changes, and optic atrophy) in 6/13 (46.15%) patients. Worm could not be identified in any of the cases. All the patients received laser photocoagulation of retina and oral albendazole treatment for a period of 30 days. With treatment, visual acuity improved in seven patients (six early stage, one late stage) and remained unchanged in six patients. Mean follow-up period was 8.69 months (range, 1–21 months). The mean central foveal thickness in the affected eye, done by optical coherence tomography, during the late stage of the disease was 188.20±40 µm (range, 111–242 µm), which was significantly thinner than the fellow eye, 238.70±36.90 µm (range, 186–319 µm), P=0.008. Conclusion DUSN is a serious vision threatening disease, which may progress to profound vision loss in the later stage of the disease. Visualization of subretinal worm is usually not possible. Treatment with high-dose albendazole therapy and laser photocoagulation may alter the blood–retinal barrier and may be useful in achieving visual recovery.

[1]  A. H. Gomes,et al.  Clinical features of 121 patients with diffuse unilateral subacute neuroretinitis. , 2012, American journal of ophthalmology.

[2]  F. Penha,et al.  Spectral Domain Optical Coherence Tomography in Diffuse Unilateral Subacute Neuroretinitis , 2011, Journal of ophthalmology.

[3]  G. Giuliari,et al.  Ocular parasitic diseases: a review on toxocariasis and diffuse unilateral subacute neuroretinitis. , 2011, Journal of pediatric ophthalmology and strabismus.

[4]  Z. A. Ghani,et al.  Intraocular nematode with diffuse unilateral subacute neuroretinitis: case report , 2011, BMC ophthalmology.

[5]  A. Berrocal,et al.  Spectral Domain OCT Findings in Diffuse Acute Unilateral Neuroretinitis (DUSN) with Subretinal Neovascularization , 2011 .

[6]  K. Ramasamy,et al.  Diffuse unilateral subacute neuroretinitis with unusual findings. , 2006, American journal of ophthalmology.

[7]  A. Bird,et al.  Progressive retinal dysfunction in diffuse unilateral subacute neuroretinitis , 2006, British Journal of Ophthalmology.

[8]  Rafael Cortez,et al.  Diffuse unilateral subacute neuroretinitis in Venezuela. , 2005, Ophthalmology.

[9]  Y. Nakashima,et al.  Clinical features and outcomes of patients with diffuse unilateral subacute neuroretinitis treated with oral albendazole. , 2005, American journal of ophthalmology.

[10]  C. A. G. Filho,et al.  Late-stage Diffuse Unilateral Subacute Neuroretinitis: Photocoagulation of the Worm does not Improve the Visual Acuity of Affected Patients , 2005, International Ophthalmology.

[11]  C. A. G. Filho,et al.  Early-stage diffuse unilateral subacute neuroretinitis: improvement of vision after photocoagulation of the worm , 2004, Eye.

[12]  E. C. de Souza,et al.  Nematode infections of the eye: toxocariasis and diffuse unilateral subacute neuroretinitis , 2001, Current opinion in ophthalmology.

[13]  R. Belfort Jr.,et al.  Hypopyon in a patient with presumptive diffuse unilateral subacute neuroretinitis , 2000, Ocular immunology and inflammation.

[14]  J. Gass,et al.  Diffuse bilateral subacute neuroretinitis: first patient with documented nematodes in both eyes. , 1999, Archives of ophthalmology.

[15]  J. Menezo,et al.  Diffuse unilateral subacute neuroretinitis in Europe. , 1999, European journal of ophthalmology.

[16]  R. Spaide OCULAR INFECTION AND IMMUNITY , 1997 .

[17]  J. Pepose,et al.  Ocular Infection and Immunity , 1996 .

[18]  M. Goldberg,et al.  Diffuse unilateral subacute neuroretinitis. Morphometric, serologic, and epidemiologic support for Baylisascaris as a causative agent. , 1993, Ophthalmology.

[19]  J. Gass,et al.  Diffuse unilateral subacute neuroretinitis in South America. , 1992, Archives of ophthalmology.

[20]  J. Gass,et al.  Oral therapy in diffuse unilateral subacute neuroretinitis. , 1992, Archives of ophthalmology.

[21]  J. Gass,et al.  Successful oral therapy for diffuse unilateral subacute neuroretinitis. , 1991, Transactions of the American Ophthalmological Society.

[22]  M. Zarbin,et al.  Ocular penetration of thiabendazole. , 1990, Archives of ophthalmology.

[23]  J. Donnelly,et al.  Retinal pigment epitheliopathy and neuroretinal degeneration in ascarid-infected eyes. , 1987, Investigative ophthalmology & visual science.

[24]  D. M. Gass,et al.  Stereoscopic Atlas of Macular Diseases: Diagnosis and Treatment , 1987 .

[25]  P. Liao,et al.  Stereoscopic Atlas of Macular Diseases. Diagnosis and Treatment , 1987, The Yale Journal of Biology and Medicine.

[26]  J. Gass,et al.  Further observations concerning the diffuse unilateral subacute neuroretinitis syndrome. , 1983, Archives of ophthalmology.

[27]  T. Meredith,et al.  Principles and Practice of Ophthalmology , 1982 .

[28]  J. D. Gass,et al.  Diffuse unilateral subacute neuroretinitis. , 1978, Ophthalmology.

[29]  W. Bénédict Nematode endophthalmitis. , 1958, The Journal of the Tennessee State Medical Association. Tennessee State Medical Association.