Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/29997
Title: Treatment of severe keratoconus hydrops with intracameral platelet-rich plasma injection
Authors: Alio, J.L.
Toprak, İbrahim
Rodriguez, A.E.
Keywords: corneal surgery
corneal transplantation
Down syndrome
keratoconus
platelet-rich plasma
sulfur hexafluoride
adult
Article
case report
clinical article
clinical examination
controlled study
cornea edema
cornea transplantation
corrected distance visual acuity
disease severity
eye pain
female
follow up
human
intraocular pressure
keratometry
optical coherence tomography
photophobia
postoperative period
priority journal
slit lamp microscopy
thrombocyte rich plasma
treatment failure
visual impairment
anterior eye chamber
complication
diagnostic imaging
drug effect
intraocular drug administration
treatment outcome
visual acuity
Adult
Anterior Chamber
Corneal Edema
Down Syndrome
Female
Humans
Injections, Intraocular
Intraocular Pressure
Keratoconus
Platelet-Rich Plasma
Tomography, Optical Coherence
Treatment Outcome
Visual Acuity
Publisher: Lippincott Williams and Wilkins
Abstract: Purpose: To present successful management of severe corneal hydrops by corneal optical coherence tomography (OCT) guidance and intracameral application of eye platelet-rich plasma (E-PRP) in a case with Down syndrome. Methods: A 36-year-old woman with Down syndrome presented with acute vision loss, pain, photophobia, and corneal edema in the left eye. Clinical examination revealed keratoconus in the right eye and extreme keratoconus with severe corneal hydrops in the left eye. Anterior segment OCT (MS-39, Costruzione Strumenti Oftalmici, Firenze, Italy) showed intrastromal cystic fluid collection and ruptured and detached Descemet membrane. The OCT-guided management of hydrops is first described in this case report. Results: Medical treatment and intracameral sulfur hexafluoride injection failed. A sterile 0.3 mL of E-PRP was injected into the anterior chamber. Clinical and anatomical improvement began from the first postoperative day, and corneal edema totally resolved at 1 week. Postoperatively, no significant side effect was noted except an early transient moderate (28 mm Hg) intraocular pressure peak. Anterior segment-OCT demonstrated dramatic normalization in corneal morphology with total disappearance of fluid in the cystic intracorneal space, closure of the DM rupture, and DM reattachment. The patient was stable during the 6-month follow-up.Conclusions:In this case, intraocular E-PRP was a promising, apparently safe, and effective treatment option in management of corneal hydrops, in which conventional approaches failed. This is the first case in the literature to describe OCT appearance of corneal hydrops and intracameral use of E-PRP for the resolution of DM rupture in acute corneal hydrops. © 2019 Wolters Kluwer Health, Inc. All rights reserved.
URI: https://hdl.handle.net/11499/29997
https://doi.org/10.1097/ICO.0000000000002070
ISSN: 0277-3740
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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