| Literature DB >> 28099337 |
Xinhua Zheng1, Ping Xie, Zizhong Hu, Weiwei Zhang, Kang Liang, Xiuying Wang, Qinghuai Liu.
Abstract
RATIONALE: A large proportion of the output of quartz infrared heat lamps is emitted as infrared radiation (IR). Retinal damage induced by IR-A and visible light on arc welders has been reported. However, case reports of retinal damage caused by quartz infrared heat lamps are rare. To the best of our knowledge, this is the first reported case of phototoxic maculopathy induced by quartz infrared heat lamps. PATIENT CONCERNS: We report a female with a 1-month history of progressive blurred vision and dysmorphopsia in her right eye after improper staring at the tubes of a quartz infrared heater. Her best corrected visual acuity of the right eye was 20/32. Optical coherence tomography revealed a defect from the ellipsoid zone to retinal pigment epithelium (RPE)/Bruch's complex layer with a diameter of 360mmat its widest. P1 amplitudes in the two central concentric rings were reduced as assessed by multifocal electroretinography. DIAGNOSES: The patient was diagnosed with phototoxic maculopathy.Entities:
Mesh:
Year: 2017 PMID: 28099337 PMCID: PMC5279082 DOI: 10.1097/MD.0000000000005830
Source DB: PubMed Journal: Medicine (Baltimore) ISSN: 0025-7974 Impact factor: 1.889
Figure 1Optical coherence tomography scan of the right eye at the first visit. Optical coherence tomography revealed a defect (wide transparent white arrow) from the ellipsoid zone to the RPE/Bruch's complex layer with a diameter of 360 μm, with a pigment disorder in adjacent areas from the external limiting membrane to RPE/Bruch's complex layer. The inset image at the bottom right corner shows the normal appearance of the macular region. RPE = retinal pigment epithelium.
Figure 2Color fundus photograph, fundus autofluorescence, fundus fluorescein angiography, visual field, and multifocal electroretinography images of the right eye at the first visit. The color fundus photograph demonstrated a light-yellow lesion with obscure boundaries at the inferior nasal region of the fovea (2A). Fundus autofluorescence revealed mottled hypofluorescence in the inferior nasal fovea (2B), consistent with fundus fluorescein angiography demonstrating mottled hyperfluorescence in the same location. There was no fluorescence leakage (2C). The visual field analysis was unremarkable (2D). P1 amplitudes in the 2 central concentric rings were reduced as assessed by multifocal electroretinography (2E).
Figure 3Optical coherence tomography scans of the right eye during the follow-up. In follow up at 1 month (3A), 3 months (3B), and 7 months (3C), her optical coherence tomography scans demonstrated that the diameter of the defect gradually shrank from 313 μm to 274 μm to 232 μm, respectively. The pigment disorder abated. A small round lump of high signal appeared in the layer of outer segments of the photoreceptors. Ten months later, at the last visit (3D), a 152 μm residual defect could be observed in the interdigitation zone and RPE/Bruch's complex layer. RPE = retinal pigment epithelium.