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Ocular Disease in Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis

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Foundations of Corneal Disease

Abstract

Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS/TEN) are on a spectrum of a rare and potentially fatal immune-mediated mucocutaneous disease. As mortality rates decrease, more survivors are left with chronic complications including those of the ocular surface. SJS/TEN can result in severe, debilitating ocular surface disease that can lead to corneal blindness. Ophthalmic care from the time of admission onwards is crucial in mitigating the acute and chronic manifestations of SJS/TEN. This chapter discusses the ocular manifestations of disease in the acute and chronic phases, systemic and topical treatment, and the future of care in SJS/TEN.

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Abbreviations

AMT:

Amniotic membrane transplantation

BKP2:

Type 2 Boston keratoprosthesis

IVIG:

Intravenous immunoglobulin

LSCD:

Limbal stem cell deficiency

MMG:

Mucous membrane graft

MOOKP:

Modified osteo-odonto-keratoprosthesis

OSDI:

Ocular surface disease index

PED:

Persistent epithelial defects

PROSE:

Prosthetic replacement of the ocular surface ecosystem

SCORTEN:

SCORe of toxic epidermal necrolysis

SJS:

Stevens-Johnson syndrome

TEN:

Toxic epidermal necrolysis

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Saeed, H.N., Rashad, R. (2020). Ocular Disease in Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis. In: Colby, K., Dana, R. (eds) Foundations of Corneal Disease. Springer, Cham. https://doi.org/10.1007/978-3-030-25335-6_10

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