Resolution of a neurotrophic keratopathy associated hypopyon with cenegermin

Purpose: We present a novel case of a neurotrophic keratopathy associated inflammatory hypopyon that resolved after initiation of therapy with cenegermin (Oxervate; Dompe, Milan, Italy), a recombinant human nerve growth factor (rhNGF). This finding illustrates the potential of cenegermin in advanced...

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Main Authors: Nick Zambino, Zeba A. Syed
Format: Article
Language:English
Published: Elsevier 2021-09-01
Series:American Journal of Ophthalmology Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2451993621001225
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spelling doaj-926144d6eae94732a472139f0cc702c82021-08-23T04:56:51ZengElsevierAmerican Journal of Ophthalmology Case Reports2451-99362021-09-0123101113Resolution of a neurotrophic keratopathy associated hypopyon with cenegerminNick Zambino0Zeba A. Syed1Cornea Service, Wills Eye Hospital, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USACorresponding author. Clinical Ophthalmology, Sidney Kimmel Medical College at Thomas Jefferson University, Cornea Service, Wills Eye Hospital, 840 Walnut Street, Suite 920, Philadelphia, PA, 19107, USA.; Cornea Service, Wills Eye Hospital, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USAPurpose: We present a novel case of a neurotrophic keratopathy associated inflammatory hypopyon that resolved after initiation of therapy with cenegermin (Oxervate; Dompe, Milan, Italy), a recombinant human nerve growth factor (rhNGF). This finding illustrates the potential of cenegermin in advanced inflammatory neurotrophic disease. Observations: A 60-year-old female with a history of herpes zoster keratitis was evaluated in our clinic for stage 2 neurotrophic keratopathy. One month later, she presented emergently with a large epithelial defect, infiltrate, and hypopyon. Three separate sets of corneal cultures returned negative. She was treated with oral antivirals and aggressive topical antibiotics with no clinical improvement. Given the presumed diagnosis of stage 3 neurotrophic keratopathy with a sterile hypopyon, she was started on cenegermin 6 times daily for 8 weeks in the absence of a corticosteroid. By 2 weeks after starting cenegermin, the epithelial defect, infiltrate, and hypopyon sizes had improved. Within 4 weeks of starting cenegermin, the hypopyon had clinically resolved. The patient was subsequently started on topical corticosteroid drops for the last 4 weeks of cenegermin therapy. Examination at the conclusion of 8 weeks of cenegermin treatment revealed a closed epithelium and minimal scar. Best-corrected visual acuity with contact lens overrefraction was 20/70. Over the course of 7 months of continued follow-up, the cornea remained epithelialized without recurrent corneal infiltration or hypopyon. Conclusions and importance: While cenegermin has been previously shown to be an effective treatment for neurotrophic keratopathy associated epithelial defects, resolution of a neurotrophic keratopathy associated inflammatory hypopyon with cenegermin is novel.http://www.sciencedirect.com/science/article/pii/S2451993621001225HypopyonCenegerminNeurotrophic keratopathy
collection DOAJ
language English
format Article
sources DOAJ
author Nick Zambino
Zeba A. Syed
spellingShingle Nick Zambino
Zeba A. Syed
Resolution of a neurotrophic keratopathy associated hypopyon with cenegermin
American Journal of Ophthalmology Case Reports
Hypopyon
Cenegermin
Neurotrophic keratopathy
author_facet Nick Zambino
Zeba A. Syed
author_sort Nick Zambino
title Resolution of a neurotrophic keratopathy associated hypopyon with cenegermin
title_short Resolution of a neurotrophic keratopathy associated hypopyon with cenegermin
title_full Resolution of a neurotrophic keratopathy associated hypopyon with cenegermin
title_fullStr Resolution of a neurotrophic keratopathy associated hypopyon with cenegermin
title_full_unstemmed Resolution of a neurotrophic keratopathy associated hypopyon with cenegermin
title_sort resolution of a neurotrophic keratopathy associated hypopyon with cenegermin
publisher Elsevier
series American Journal of Ophthalmology Case Reports
issn 2451-9936
publishDate 2021-09-01
description Purpose: We present a novel case of a neurotrophic keratopathy associated inflammatory hypopyon that resolved after initiation of therapy with cenegermin (Oxervate; Dompe, Milan, Italy), a recombinant human nerve growth factor (rhNGF). This finding illustrates the potential of cenegermin in advanced inflammatory neurotrophic disease. Observations: A 60-year-old female with a history of herpes zoster keratitis was evaluated in our clinic for stage 2 neurotrophic keratopathy. One month later, she presented emergently with a large epithelial defect, infiltrate, and hypopyon. Three separate sets of corneal cultures returned negative. She was treated with oral antivirals and aggressive topical antibiotics with no clinical improvement. Given the presumed diagnosis of stage 3 neurotrophic keratopathy with a sterile hypopyon, she was started on cenegermin 6 times daily for 8 weeks in the absence of a corticosteroid. By 2 weeks after starting cenegermin, the epithelial defect, infiltrate, and hypopyon sizes had improved. Within 4 weeks of starting cenegermin, the hypopyon had clinically resolved. The patient was subsequently started on topical corticosteroid drops for the last 4 weeks of cenegermin therapy. Examination at the conclusion of 8 weeks of cenegermin treatment revealed a closed epithelium and minimal scar. Best-corrected visual acuity with contact lens overrefraction was 20/70. Over the course of 7 months of continued follow-up, the cornea remained epithelialized without recurrent corneal infiltration or hypopyon. Conclusions and importance: While cenegermin has been previously shown to be an effective treatment for neurotrophic keratopathy associated epithelial defects, resolution of a neurotrophic keratopathy associated inflammatory hypopyon with cenegermin is novel.
topic Hypopyon
Cenegermin
Neurotrophic keratopathy
url http://www.sciencedirect.com/science/article/pii/S2451993621001225
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