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Journal articles on the topic 'Keratopathy'

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1

Watson, A. P., A. B. Tullo, M. G. Kerr-Muir, A. E. A. Ridgway, and D. R. Lucas. "Arborescent bacterial keratopathy (infectious crystalline keratopathy)." Eye 2, no. 5 (1988): 517–22. http://dx.doi.org/10.1038/eye.1988.101.

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2

Szentmáry, Nóra, Kitti Kormányos, Gábor Tóth, et al. "Szemészeti tünetek és szemészeti társbetegségek monoklonális gammopathiával járó kórképekben." Hematológia–Transzfuziológia 54, no. 2 (2021): 82–88. http://dx.doi.org/10.1556/2068.2021.54.2.4.

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Összefoglaló. Célkitűzés: A monoklonális fehérjetermeléssel járó haematológiai kórképek szemészeti tüneteinek és szemészeti társbetegségeinek összefoglalása irodalmi adatok alapján. Módszer: A Pubmedben rendelkezésre álló adatok kigyűjtése, elemzése és összefoglalása. Eredmények: Immunglobulin-lerakódás a szem szövetei közül leggyakrabban a szaruhártyában figyelhető meg (paraproteinaemiás vagy immuntaktoid keratopathia). A monoklonális fehérjeszaporulattal járó plazmasejtes betegség gyakoribb szemészeti jelei pedig a paraproteinaemiás keratopathia mellett a kristályhordozó histiocytosis (CSH),
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3

Yeung, Alexander, and Surendar Dwarakanathan. "Diabetic keratopathy." Disease-a-Month 67, no. 5 (2021): 101135. http://dx.doi.org/10.1016/j.disamonth.2021.101135.

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4

Karp, C. L., and I. Y. Scott. "CACTUS KERATOPATHY." Cornea 15, no. 2 (1996): 215. http://dx.doi.org/10.1097/00003226-199603000-00019.

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5

Trujillo, Fernando, Diemngoc Dang, and Tomy Starck. "Xylene Keratopathy." Cornea 22, no. 1 (2003): 88–90. http://dx.doi.org/10.1097/00003226-200301000-00023.

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6

DeRosa, Anthony J. "Toxic Keratopathy." International Ophthalmology Clinics 38, no. 4 (1998): 15–22. http://dx.doi.org/10.1097/00004397-199803840-00004.

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7

U??akhan, ??m??r ??, Ayfer Kanpolat, Nurg??l Ylmaz, and Muhip ??zkan. "Amiodarone Keratopathy." Eye & Contact Lens: Science & Clinical Practice 31, no. 4 (2005): 148–57. http://dx.doi.org/10.1097/01.icl.0000165283.36659.35.

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8

Manabe, Reizo, Mamoru Matsuda, and Yuichi Ohashi. "Diabetic Keratopathy." Cornea 6, no. 2 (1987): 154. http://dx.doi.org/10.1097/00003226-198706020-00037.

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9

Rao, Gullapalli N. "Diabetic Keratopathy." Cornea 6, no. 2 (1987): 156. http://dx.doi.org/10.1097/00003226-198706020-00048.

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10

Forsius, Henrik. "LIPID KERATOPATHY." Acta Ophthalmologica 39, no. 2 (2009): 272–83. http://dx.doi.org/10.1111/j.1755-3768.1961.tb00259.x.

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11

Dailey, John R., Robert E. Parnes, and Ali Aminlari. "Glutaraldehyde Keratopathy." American Journal of Ophthalmology 115, no. 2 (1993): 256–58. http://dx.doi.org/10.1016/s0002-9394(14)73936-4.

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12

Milman, Tatyana, Andrew A. Kao, David Chu, et al. "Paraproteinemic Keratopathy." Ophthalmology 122, no. 9 (2015): 1748–56. http://dx.doi.org/10.1016/j.ophtha.2015.05.029.

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13

Del Valle, Maria, and Ramon L. Font. "Achromobacter Keratopathy." Ophthalmology 116, no. 1 (2009): 165–165. http://dx.doi.org/10.1016/j.ophtha.2008.09.031.

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14

Gonçalves, Eliana D., Fabiana dos S. Paris, José Álvaro P. Gomes, Liliane Kanecadan, and Mauro Campos. "Bullous Keratopathy." Ophthalmology 118, no. 11 (2011): 2303–2303. http://dx.doi.org/10.1016/j.ophtha.2011.05.034.

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15

Peddada, Krishi, Brett Campbell, Briana Ply, and An Vo. "Neurotrophic Keratopathy." Advances in Ophthalmology and Optometry 4 (August 2019): 275–82. http://dx.doi.org/10.1016/j.yaoo.2019.05.003.

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16

Dua, Harminder S., Dalia G. Said, Elisabeth M. Messmer, et al. "Neurotrophic keratopathy." Progress in Retinal and Eye Research 66 (September 2018): 107–31. http://dx.doi.org/10.1016/j.preteyeres.2018.04.003.

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17

Frazer, D. G., M. F. J. Armstrong, and D. B. Archer. "Compression Keratopathy." American Journal of Ophthalmology 102, no. 2 (1986): 208–10. http://dx.doi.org/10.1016/0002-9394(86)90146-7.

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18

Holland, Edward J., Cy A. Stein, Alan G. Palestine, et al. "Suramin Keratopathy." American Journal of Ophthalmology 106, no. 2 (1988): 216–20. http://dx.doi.org/10.1016/0002-9394(88)90838-0.

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19

Ezugbaya, Maggie B., Sergey Y. Astakhov, Inna A. Riks, et al. "Neurotrophic keratopathy and Wallenberg – Zakharchenko syndrome: a clinical case." Ophthalmology Journal 14, no. 3 (2021): 83–90. http://dx.doi.org/10.17816/ov79199.

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BACKGROUND: Degenerative changes of cornea after transection of the trigeminal nerve were first described by F. Magendie in 1824. Neurotrophic keratopathy is considered to be an orphan disease which lately has been recognized more and more often. According to literature data, neurotropchic keratopathy affects 5 individuals in 10,000. The diagnosis is difficult due to the lack of information about this condition, the rare occurrence and the presence of a large number of etiological factors.
 AIM: To determine the causes of the neurotrophic keratopathy development and the treatment tactics
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20

Mamtani, Nidhi, Sagarika Snehi, Kanishk Singh, and Rajesh Pattebahadur. "Ripasudil’s paradox: bullous keratopathy with honeycomb twist." BMJ Case Reports 17, no. 12 (2024): e261052. https://doi.org/10.1136/bcr-2024-261052.

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We present a case of a male patient in his mid-50s who presented with bullous keratopathy secondary to an anterior chamber intraocular lens, complicated by superimposed honeycomb keratopathy while on ripasudil 0.4%. The bullous keratopathy was characterised by generalised microcystic epithelial oedema, alongside more centrally located, variable-sized macrocystic epithelial oedema with a honeycomb appearance. Discontinuation of ripasudil resulted in the resolution of the honeycomb keratopathy, although with the persistence of pre-existing microcystic corneal oedema. This case highlights the com
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21

Klaassen-Broekema, N., and O. P. Van Bijsterveld. "Rapid Progression of Band-Shaped Keratopathy with Early Central Localisation in a Patient on Chronic Dialytic Treatment." European Journal of Ophthalmology 4, no. 2 (1994): 126–29. http://dx.doi.org/10.1177/112067219400400210.

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This clinical study reports on an unusual start of a band-shaped keratopathy in a patient with diabetic nephropathy on dialytic treatment. The earliest corneal manifestations were centrally located small greyish-white disc-shaped lesions evenly distributed in the interpalpebral area in the left eye. Later a typical peripheral band-shaped keratopathy developed. In the course of the observation period the peripheral keratopathy rapidly spread towards the centre, finally resulting in a complete band-shaped keratopathy in which only the most central original disc-shaped lesions could be identified
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22

Khambati, Alisha, Patrick Shean-Young Lee, Shabbir Khambati, and Mark McDermott. "Removal of band keratopathy involving a LASIK flap with Amoils brush and ethylenediaminetetraacetic acid chelation." Journal of Cataract & Refractive Surgery Online Case Reports 13 (January 2025): e00147. https://doi.org/10.1097/j.jcro.0000000000000147.

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Introduction: To report a new method for ethylenediaminetetraacetic acid (EDTA) chelation with the use of an Amoils brush to debride calcium band keratopathy involving a laser-assisted in situ keratomileusis (LASIK) flap. Patient and Clinical Findings: A 77-year-old man with a history of bilateral LASIK presented with visually significant band keratopathy involving the flap. Diagnosis, Intervention, and Outcomes: We report the successful removal of the band keratopathy using EDTA chelation and debridement with an Amoils brush to prevent flap dislodgment. 1 month postoperatively, the patient ex
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23

Hsu, Hung-Jui, Chia-Yi Lee, Kun-Lin Yang, et al. "The Development of Keratopathy after Surgery-Indicated Chronic Rhinosinusitis: A Population-Based Cohort Study." International Journal of Environmental Research and Public Health 16, no. 7 (2019): 1218. http://dx.doi.org/10.3390/ijerph16071218.

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The aim of the present study was to evaluate the risk of developing keratopathy in patients with surgery-indicated chronic rhinosinusitis (CRS) via the National Health Insurance Research Database in Taiwan. Patients with a diagnostic code of CRS and who received functional endoscopic sinus surgery (FESS) were considered to have surgery-indicated CRS. The exclusion criteria were legal blindness, an ocular tumor, eyeball removal or previous keratopathy, and each individual in the study group was matched to four non-CRS patients by age and sex. The outcome was set as the occurrence of keratopathy
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24

Ikegawa, Yasuhito, Atsushi Shiraishi, Yasuhito Hayashi, Akiyoshi Ogimoto, and Yuichi Ohashi. "In Vivo Confocal Microscopic Observations of Vortex Keratopathy in Patients with Amiodarone-Induced Keratopathy and Fabry Disease." Journal of Ophthalmology 2018 (2018): 1–7. http://dx.doi.org/10.1155/2018/5315137.

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Purpose. To compare the morphology of two types of vortex keratopathy: amiodarone-induced keratopathy and the Fabry disease-associated keratopathy. Patients and Methods. Eight patients who were receiving oral amiodarone therapy and 3 patients with Fabry disease, a mother and her 2 daughters, were examined by slit-lamp biomicroscopy and in vivo confocal microscopy (IVCM) regularly. Results. Amiodarone-induced keratopathy developed in 7 of the 8 patients, and it was detected as early as 7 days by IVCM and 14 days by slit-lamp biomicroscopy. The in vivo confocal microscopic images showed a cluste
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25

AlGhadeer, Huda, Thamer Bukhari, and Mohammed AlAmry. "Toxic Keratopathy Induced by Self-Application of Seawater." Middle East African Journal of Ophthalmology 29, no. 1 (2022): 63–65. http://dx.doi.org/10.4103/meajo.meajo_313_21.

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To report a case of toxic keratopathy secondary to the self-application of seawater eye drops. A 60-year-old male who presented with unexplained unilateral decrease in vision and corneal thinning. Best-corrected visual acuity was 20/400 OD, slit-lamp examination indicated diffuse corneal edema with central thinning, intact sensation, and no vascularization. Laboratory analysis of the eye drops in conjunction with clinical symptoms and findings was consistent with toxic keratopathy. Toxic keratopathy can masquerade as the other forms of keratopathy, and a thorough history taking and laboratory
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26

Mahajan, Deepti, Anil Verma, and Rajesh Sharma. "Amiodarone-induced vortex keratopathy at a low maintenance dose." Asian Journal of Ophthalmology 17, no. 2 (2020): 170–72. http://dx.doi.org/10.35119/asjoo.v17i2.553.

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Vortex keratopathy is a common side effect of amiodarone, which is a class III antiarrhythmic agent. We describe a 50-year-old man who developed vortex keratopahy with amiodarone 200 mg BD for atrial fibrillation since two years. The daily (400 mg/day) and cumulative dose (100 g) combined with the length of therapy is associated with the toxicity. Toxic effects may also be observed at lower maintenance doses, as observed in this patient. This case indicates that multi-organ toxicity due to amiodarone may develop even with short-term use and a low maintenance dose. Having been off the medicatio
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27

Denisko, M. S., T. A. Zhigalskaya, and O. I. Krivosheina. "The role of inflammation in pathogenesis of bullous kerathopathy." Modern technologies in ophtalmology, no. 6 (October 29, 2023): 67–70. http://dx.doi.org/10.25276/2312-4911-2022-6-67-70.

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Background. Bullous keratopathy is a chronic steadily progressive disease that leads to a significant decrease in vision and is accompanied by the appearance of a pronounced pain syndrome. Currently, the role of cytokines in the pathogenesis of the disease remains insufficiently studied. The aim of the study was to study the level of proinflammatory cytokines of the lacrimal fluid in bullous keratopathy. Results. There was a statistically significant increase of the level of proinflammatory cytokines in the lacrimal fluid of patients with bullous keratopathy: interleukin (IL) 1β by 3.6 times (
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28

Choi, Woo Chul, Sang Kyung Choi, and Jin Hak Lee. "Silicone oil keratopathy." Korean Journal of Ophthalmology 7, no. 2 (1993): 65. http://dx.doi.org/10.3341/kjo.1993.7.2.65.

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29

Shinisha D P, Siddharam S. Janti, and Stephen Sudhakar K. "Moxifloxacin induced keratopathy." Indian Journal of Clinical and Experimental Ophthalmology 7, no. 3 (2021): 594–95. http://dx.doi.org/10.18231/j.ijceo.2021.116.

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Moxifloxacin being a broad-spectrum fluoroquinolones is widely used in various ocular disorders by ophthalmologists for its broad-spectrum of action. Various studies on moxifloxacin use indicates it as a safe drug and ocular toxicity following moxifloxacin use is very rare. We present a rare case of moxifloxacin induced keratopathy post cataract surgery.
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30

TABBARA, KHALID F. "Climatic Droplet Keratopathy." International Ophthalmology Clinics 26, no. 4 (1986): 63–68. http://dx.doi.org/10.1097/00004397-198602640-00006.

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31

Stern, George A. "Infectious Crystalline Keratopathy." International Ophthalmology Clinics 33, no. 1 (1993): 1–7. http://dx.doi.org/10.1097/00004397-199303310-00003.

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32

Pricopie, Stefan, Sanziana Istrate, Liliana Voinea, Costin Leasu, Vanessa Paun, and Radu Ciuluvica. "Pseudophakic bullous keratopathy." Romanian Journal of Ophthalmology 61, no. 2 (2017): 90–94. http://dx.doi.org/10.22336/rjo.2017.17.

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33

Chilov, Michael N., Con N. Moshegov, and Frances Booth. "Unilateral amiodarone keratopathy." Clinical and Experimental Ophthalmology 33, no. 6 (2005): 666–68. http://dx.doi.org/10.1111/j.1442-9071.2005.01121.x.

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34

Pye, David C., and H. Barry Collin. "Aphakic bullous keratopathy." Clinical and Experimental Optometry 69, no. 2 (1986): 71–72. http://dx.doi.org/10.1111/j.1444-0938.1986.tb04571.x.

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35

Samples, John R., Stephen D. Baumgartner, and Perry S. Binder. "Infectious Crystalline Keratopathy." Cornea 4, no. 2 (1985): 118???126. http://dx.doi.org/10.1097/00003226-198502000-00007.

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36

Pandit, Rahul T. "Dendriform Filamentary Keratopathy." Cornea 28, no. 1 (2009): 123–25. http://dx.doi.org/10.1097/ico.0b013e318182ed19.

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37

Seitzman, Gerami D., Erich C. Strauss, and Todd P. Margolis. "“Steel Wool Keratopathy”." Cornea 25, no. 6 (2006): 742–44. http://dx.doi.org/10.1097/01.ico.0000214235.51732.8e.

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38

Porter, Ashley J., Graham A. Lee, and Albert S. Jun. "Infectious crystalline keratopathy." Survey of Ophthalmology 63, no. 4 (2018): 480–99. http://dx.doi.org/10.1016/j.survophthal.2017.10.008.

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39

Ormerod, L. David, Kathryn L. Ruoff, David M. Meisler, et al. "Infectious Crystalline Keratopathy." Ophthalmology 98, no. 2 (1991): 159–69. http://dx.doi.org/10.1016/s0161-6420(91)32321-2.

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40

Freedman, Jeffrey. "Climatic Droplet Keratopathy." Ophthalmology 101, no. 10 (1994): 1646. http://dx.doi.org/10.1016/s0161-6420(94)31122-5.

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41

Sutton, Gerard L., Ross C. Miller, and Lyon P. Robinson. "Infectious crystalline keratopathy." Australian and New Zealand Journal of Ophthalmology 18, no. 2 (1990): 151–54. http://dx.doi.org/10.1111/j.1442-9071.1990.tb00606.x.

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42

Horsburgh, Bradley, Lawrence W. Hirst, Geoff A. Hoole, Kevin Vandeleur Snr, W. Richard Green, and R. Michael Whitby. "Infectious crystalline keratopathy." Australian and New Zealand Journal of Ophthalmology 22, no. 1 (1994): 69–72. http://dx.doi.org/10.1111/j.1442-9071.1994.tb01699.x.

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43

Arentsen, Juan J., Elisabeth J. Cohen, Steven E. Brady, et al. "Pseudophakic Bullous Keratopathy." American Journal of Ophthalmology 106, no. 3 (1988): 264–69. http://dx.doi.org/10.1016/s0002-9394(14)76615-2.

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44

Ormerod, L. David, H. Barry Collin, Claes H. Dohlman, Joseph L. Craft, Jane F. Desforges, and Daniel M. Albert. "Paraproteinemic Crystalline Keratopathy." Ophthalmology 95, no. 2 (1988): 202–12. http://dx.doi.org/10.1016/s0161-6420(88)33200-8.

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45

Schwab, Ivan R., and Richard L. Abbott. "Toxic Ulcerative Keratopathy." Ophthalmology 96, no. 8 (1989): 1187–93. http://dx.doi.org/10.1016/s0161-6420(89)32752-7.

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46

Gordon, Judy F., Penny Asbell, Richard Norden, and Richard Eiferman. "Toxic Ulcerative Keratopathy." Ophthalmology 97, no. 9 (1990): 1091. http://dx.doi.org/10.1016/s0161-6420(90)38018-8.

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47

Sakuma, T. "Amiodarone-induced Keratopathy." Japanese Journal of Ophthalmology 45, no. 6 (2001): 682. http://dx.doi.org/10.1016/s0021-5155(01)00444-0.

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48

Carpel, Emmett F., J. Douglas Cameron, and Mark R. Wick. "Circumferential nodulocystic keratopathy." Graefe's Archive for Clinical and Experimental Ophthalmology 226, no. 6 (1988): 505–9. http://dx.doi.org/10.1007/bf02169196.

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49

James, C. B., P. J. McDonnell, and M. G. Falcon. "Infectious crystalline keratopathy." British Journal of Ophthalmology 72, no. 8 (1988): 628–30. http://dx.doi.org/10.1136/bjo.72.8.628.

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50

DUA, HS. "Infectious crystalline keratopathy." Acta Ophthalmologica 87 (September 2009): 0. http://dx.doi.org/10.1111/j.1755-3768.2009.1322.x.

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