scholarly journals Intravitreal Ranibizumab and Laser Photocoagulation in the Management of Idiopathic Juxtafoveolar Retinal Telangiectasia Type 1: A Case Report

2012 ◽  
Vol 3 (3) ◽  
pp. 298-303 ◽  
Author(s):  
Angela Ciarnella ◽  
Sara Verrilli ◽  
Vito Fenicia ◽  
Cristina Mannino ◽  
Alessandro Cutini ◽  
...  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Martin Pencak ◽  
Miroslav Veith

Abstract Background To present a case report of a patient with a mixed choroidal neovascular membrane (CNV) with an asymmetric response to ranibizumab diagnosed on optical coherence tomography angiography (OCTa). Case presentation A 61-year-old male was referred to our department in September 2017 due to decreased vision in his left eye. Best-corrected visual acuity (BCVA) was 43 Early Treatment Diabetic Retinopathy Study (ETDRS) letters in the left eye. Macular edema was present in the left eye, and a mixed CNV was identified on the OCTa. Therapy with intravitreal ranibizumab was commenced. After 5 ranibizumab injections, the BCVA was 42 ETDRS letters, and considerable intraretinal edema was still present. OCTa showed a resolution of the type 2 lesion of the mixed CNV; however, the type 1 lesion had continued to grow. The patient was then switched to intravitreal aflibercept. After 3 monthly aflibercept injections, the BCVA improved to 53 ETDRS letters, and a reduction of the edema was observed on the optical coherence tomography (OCT). OCTa showed a decrease in both the area and vessel density in the type 1 lesion of the CNV. Therapy with aflibercept was continued; however, while the intraretinal edema continued to improve, atrophy developed in the macula and the BCVA worsened to 43 ETDRS letters. Conclusions Ranibizumab nonresponse in a neovascular age-related macular degeneration is not uncommon. However, to our knowledge, this is the first described case of an asymmetric response to ranibizumab in a mixed CNV. While the type 2 lesion of the CNV reacted swiftly to the ranibizumab therapy, the type 1 lesion continued to grow. As with some other cases of ranibizumab resistance, switching to aflibercept proved effective.


2019 ◽  
Vol 33 (1-4) ◽  
pp. 29-31
Author(s):  
Shilpi H. Narnaware ◽  
Prashant K. Bawankule

Aim: A case which highlights the challenges faced in treating a case of type 1 early treatment of retinopathy of prematurity (ETROP) with persistent corneal defect. Case Report: We report a case of a preterm boy born at 28 weeks with birth weight of 700 g who presented with persistent corneal defect along with type 1 ETROP disease. Because of the inability to complete LASER, intravitreal ranibizumab was given as a rescue therapy to buy some time. But unfortunately, baby succumbed to disease because of associated systemic problems. Conclusion: ROP can present with persistent corneal defect which can challenge the treatment of underlying pathology.


2006 ◽  
Vol 19 (2) ◽  
pp. 213
Author(s):  
Tae Kyu Park ◽  
Kyung Ream Han ◽  
Dong Wook Shin ◽  
Young Joo Lee ◽  
Chan Kim

2018 ◽  
Author(s):  
A Emile J Hendriks ◽  
Ross L Ewen ◽  
Yoke Sin Hoh ◽  
Nazia Bhatti ◽  
Rachel M Williams ◽  
...  

2019 ◽  
Author(s):  
Rolly Junior Louzolo-Kimbembe ◽  
Ghizlane El Mghari ◽  
Nawal El Ansari

Author(s):  
Loukil Fatma ◽  
Pinto Sara ◽  
Tatulashivili Sopio ◽  
Carlier Lea ◽  
Bihan Helène

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