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The Evolution of Full Thickness Macular Hole After Short Exposure to High Powered Hand-held Laser Pointer

Keshet, Yariv; Weseley, Peter E; Ceisler, Emily J; Ngo, Wei Kiong; Salcedo, Alfredo; Walia, Jay; Spaide, Richard F
PURPOSE/OBJECTIVE:To report a case of a full thickness macular hole (FTMH) after exposure to an extremely powerful handheld laser pointer. METHODS:We evaluated a 14-year-old male with a laser induced FTMH one month after a momentary exposure to a 5000 mW blue laser pointer. Imaging modalities including fundus color, autofluorescence, and spectral domain optical coherence tomography (SD-OCT), acquired both at our clinic and by the referring physician soon after the injury, are used to describe the clinical evolution of the case. RESULTS:Soon after the injury an intensely white, circular opacification of the retina approximately 400 µm in diameter was seen in the fovea. Early SD-OCT images showed full thickness hyperreflectivity, likely representing tissue necrosis. One month later, a FTMH and eradication of the retinal pigment epithelium at its base were evident in the fundus color, autofluorescence and SD-OCT images. CONCLUSION/CONCLUSIONS:High power laser pointers have become easily available online. The presenting findings after exposure to such high-power devices are distinct from those reported after exposure to weaker laser pointers. While long exposure to weaker lasers typically produces extensive, calligraphic figures and yellow placoid lesions involving only the outer retina, in our case a very brief exposure led to focal, full-thickness injury of the fovea.
PMID: 36730459
ISSN: 1937-1578
CID: 5420372

Simultaneous scleral buckling and Baerveldt glaucoma implant surgery in patients with coexisting retinal detachment and glaucoma [Meeting Abstract]

Dias, RH; Will, DV; Sidoti, PA; Gentile, RC; Weseley, P
ISI:000223338000907
ISSN: 0146-0404
CID: 3980622

Lattice degeneration of the retina and the pigment dispersion syndrome

Weseley, P; Liebmann, J; Walsh, J B; Ritch, R
Retinal detachment occurs more frequently in patients with pigment dispersion syndrome. We evaluated the incidence of peripheral retinal abnormalities known to predispose to rhegmatogenous retinal detachment in a consecutive series of 60 patients with pigment dispersion syndrome with or without glaucoma. Lattice degeneration was present in at least one eye of 12 patients (20%). Seven patients had bilateral lesions. Full-thickness retinal breaks were found in seven patients (11.7%) and two patients (3.3%) had asymptomatic rhegmatogenous retinal detachments that required scleral buckle procedures. The incidence of lattice degeneration and full-thickness retinal breaks appears to be increased in this group of patients, and may be responsible for the increased risk of rhegmatogenous detachment.
PMID: 1443014
ISSN: 0002-9394
CID: 4049222

PIGMENT DISPERSION SYNDROME AND LATTICE DEGENERATION OF THE RETINA [Meeting Abstract]

LIEBMANN, J; WESELEY, P; WALSH, J; RITCH, R; MARMOR, M
ISI:A1992HK13500204
ISSN: 0146-0404
CID: 52041

RHEGMATOGENOUS RETINAL-DETACHMENT AFTER INITIATION OF OCUSERT THERAPY [Letter]

WESELEY, P; LIEBMANN, J; RITCH, R
ISI:A1991GJ13100017
ISSN: 0002-9394
CID: 3980642