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Salzmann nodular degeneration: prevalence, impact, and management strategies
This review will summarize the clinical and histological presentation of Salzmann nodular degeneration (SND), its prevalence and risk factors, potential underlying mechanisms, diagnostic tools, management options, and impact on cataract surgery and co-morbid ocular surface diseases. PubMed review of...
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Published in: | Clinical ophthalmology (Auckland, N.Z.) N.Z.), 2019-07, Vol.13, p.1305-1314 |
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description | This review will summarize the clinical and histological presentation of Salzmann nodular degeneration (SND), its prevalence and risk factors, potential underlying mechanisms, diagnostic tools, management options, and impact on cataract surgery and co-morbid ocular surface diseases.
PubMed review of 44 articles published between 1976 and 2018.
SND is a corneal disease characterized by whitish gray or bluish nodules on the peripheral or central cornea. The clinical presentation of SND is variable and the nodules can be asymptomatic or cause foreign body sensation and/or blurred vision. Histologically, SND appears as subepithelial nodules with thin overlying epithelium, disrupted or absent Bowman's layer, and activated fibroblasts within the nodule. SND pathogenesis is not fully understood but is thought to involve poor epithelial protection and disruption of the epithelial-stromal interface, allowing for penetration of epithelially derived growth factors into the stroma and subsequent activation of stromal fibroblasts, eventually leading to sub-epithelial deposition of disorganized extracellular membrane components. SND most commonly occurs in Caucasian females in a bimodal distribution, occurring in the fifth or eighth and ninth decades of life. Risk factors for SND include ocular surface diseases and surgery. Surgical intervention is recommended in individuals with symptomatic nodules - primarily superficial keratectomy performed with or without intraoperative mitomycin C, photokeratectomy, and/or amniotic membrane transplantation. These procedures have been successful in removing the lesion and reducing corneal irregularity, but have variable recurrence rates (0-31%).
The pathogenesis of SND is complex and multifactorial. Advances in diagnostic and treatment modalities have allowed for earlier and more accurate diagnosis and effective treatment of SND. |
doi_str_mv | 10.2147/OPTH.S166280 |
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PubMed review of 44 articles published between 1976 and 2018.
SND is a corneal disease characterized by whitish gray or bluish nodules on the peripheral or central cornea. The clinical presentation of SND is variable and the nodules can be asymptomatic or cause foreign body sensation and/or blurred vision. Histologically, SND appears as subepithelial nodules with thin overlying epithelium, disrupted or absent Bowman's layer, and activated fibroblasts within the nodule. SND pathogenesis is not fully understood but is thought to involve poor epithelial protection and disruption of the epithelial-stromal interface, allowing for penetration of epithelially derived growth factors into the stroma and subsequent activation of stromal fibroblasts, eventually leading to sub-epithelial deposition of disorganized extracellular membrane components. SND most commonly occurs in Caucasian females in a bimodal distribution, occurring in the fifth or eighth and ninth decades of life. Risk factors for SND include ocular surface diseases and surgery. Surgical intervention is recommended in individuals with symptomatic nodules - primarily superficial keratectomy performed with or without intraoperative mitomycin C, photokeratectomy, and/or amniotic membrane transplantation. These procedures have been successful in removing the lesion and reducing corneal irregularity, but have variable recurrence rates (0-31%).
The pathogenesis of SND is complex and multifactorial. Advances in diagnostic and treatment modalities have allowed for earlier and more accurate diagnosis and effective treatment of SND.</description><identifier>ISSN: 1177-5467</identifier><identifier>ISSN: 1177-5483</identifier><identifier>EISSN: 1177-5483</identifier><identifier>DOI: 10.2147/OPTH.S166280</identifier><identifier>PMID: 31413538</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Cataract extraction ; Cataracts ; cornea ; diagnosis ; Ecosystems ; Epidemiology ; Epithelium ; Eye diseases ; Eye surgery ; imaging ; Lasers ; Microscopy ; Mitomycin ; Ophthalmology ; Prostheses ; Review ; Salzmann nodular degeneration ; Strategic planning (Business) ; Surgery ; Therapeutics ; Tomography ; Topography ; treatment</subject><ispartof>Clinical ophthalmology (Auckland, N.Z.), 2019-07, Vol.13, p.1305-1314</ispartof><rights>COPYRIGHT 2019 Dove Medical Press Limited</rights><rights>2019. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 Paranjpe et al. 2019 Paranjpe et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c576t-b4633f500c725168ab543a18cf1d863a0826827b8f0c72b9d6b3442702d658de3</citedby><orcidid>0000-0002-3124-2462</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2274556473/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2274556473?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31413538$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Paranjpe, Vikram</creatorcontrib><creatorcontrib>Galor, Anat</creatorcontrib><creatorcontrib>Monsalve, Pedro</creatorcontrib><creatorcontrib>Dubovy, Sander R</creatorcontrib><creatorcontrib>Karp, Carol L</creatorcontrib><title>Salzmann nodular degeneration: prevalence, impact, and management strategies</title><title>Clinical ophthalmology (Auckland, N.Z.)</title><addtitle>Clin Ophthalmol</addtitle><description>This review will summarize the clinical and histological presentation of Salzmann nodular degeneration (SND), its prevalence and risk factors, potential underlying mechanisms, diagnostic tools, management options, and impact on cataract surgery and co-morbid ocular surface diseases.
PubMed review of 44 articles published between 1976 and 2018.
SND is a corneal disease characterized by whitish gray or bluish nodules on the peripheral or central cornea. The clinical presentation of SND is variable and the nodules can be asymptomatic or cause foreign body sensation and/or blurred vision. Histologically, SND appears as subepithelial nodules with thin overlying epithelium, disrupted or absent Bowman's layer, and activated fibroblasts within the nodule. SND pathogenesis is not fully understood but is thought to involve poor epithelial protection and disruption of the epithelial-stromal interface, allowing for penetration of epithelially derived growth factors into the stroma and subsequent activation of stromal fibroblasts, eventually leading to sub-epithelial deposition of disorganized extracellular membrane components. SND most commonly occurs in Caucasian females in a bimodal distribution, occurring in the fifth or eighth and ninth decades of life. Risk factors for SND include ocular surface diseases and surgery. Surgical intervention is recommended in individuals with symptomatic nodules - primarily superficial keratectomy performed with or without intraoperative mitomycin C, photokeratectomy, and/or amniotic membrane transplantation. These procedures have been successful in removing the lesion and reducing corneal irregularity, but have variable recurrence rates (0-31%).
The pathogenesis of SND is complex and multifactorial. Advances in diagnostic and treatment modalities have allowed for earlier and more accurate diagnosis and effective treatment of SND.</description><subject>Cataract extraction</subject><subject>Cataracts</subject><subject>cornea</subject><subject>diagnosis</subject><subject>Ecosystems</subject><subject>Epidemiology</subject><subject>Epithelium</subject><subject>Eye diseases</subject><subject>Eye surgery</subject><subject>imaging</subject><subject>Lasers</subject><subject>Microscopy</subject><subject>Mitomycin</subject><subject>Ophthalmology</subject><subject>Prostheses</subject><subject>Review</subject><subject>Salzmann nodular degeneration</subject><subject>Strategic planning (Business)</subject><subject>Surgery</subject><subject>Therapeutics</subject><subject>Tomography</subject><subject>Topography</subject><subject>treatment</subject><issn>1177-5467</issn><issn>1177-5483</issn><issn>1177-5483</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt2LEzEUxQdR3A9981kGBNmHtuY7qQ_Csqi7UFhh1-eQSe5Mp8wkNZlZ0L_ejK2lFclDws3vnktOTlG8wWhBMJMf7r893i4esBBEoWfFOcZSzjlT9PnhLORZcZHSBiFBkJIvizOKGaacqvNi9WC6X73xvvTBjZ2JpYMGPEQztMF_LLcRnkwH3sKsbPutscOsNN6VucU00IMfyjRkGJoW0qviRW26BK_3-2Xx_cvnx5vb-er-693N9WpuuRTDvGKC0pojZCXhWChTcUYNVrbGTglqkCJCEVmpeiKqpRMVZYxIRJzgygG9LO52ui6Yjd7Gtjfxpw6m1X8KITbaxKG1HWggS6vM0tYWMcaWrgLLOWBrHKO1YFXW-rTT2o5VD87mF0XTnYie3vh2rZvwpIUQFEmZBa72AjH8GCENum-Tha4zHsKYNCGSSoUVphl99w-6CWP02aqJYpwLJo-oJhuvW1-HPNdOovpaIIIQJ5xkavEfKi8HfWuDh7rN9ZOG90cNazDdsE6hG6d_TqfgbAfaGFKKUB_MwEhPkdNT5PQ-chl_e2zgAf6bMfobl2bOzg</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Paranjpe, Vikram</creator><creator>Galor, Anat</creator><creator>Monsalve, Pedro</creator><creator>Dubovy, Sander R</creator><creator>Karp, Carol L</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3124-2462</orcidid></search><sort><creationdate>20190701</creationdate><title>Salzmann nodular degeneration: prevalence, impact, and management strategies</title><author>Paranjpe, Vikram ; Galor, Anat ; Monsalve, Pedro ; Dubovy, Sander R ; Karp, Carol L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c576t-b4633f500c725168ab543a18cf1d863a0826827b8f0c72b9d6b3442702d658de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Cataract extraction</topic><topic>Cataracts</topic><topic>cornea</topic><topic>diagnosis</topic><topic>Ecosystems</topic><topic>Epidemiology</topic><topic>Epithelium</topic><topic>Eye diseases</topic><topic>Eye surgery</topic><topic>imaging</topic><topic>Lasers</topic><topic>Microscopy</topic><topic>Mitomycin</topic><topic>Ophthalmology</topic><topic>Prostheses</topic><topic>Review</topic><topic>Salzmann nodular degeneration</topic><topic>Strategic planning (Business)</topic><topic>Surgery</topic><topic>Therapeutics</topic><topic>Tomography</topic><topic>Topography</topic><topic>treatment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paranjpe, Vikram</creatorcontrib><creatorcontrib>Galor, Anat</creatorcontrib><creatorcontrib>Monsalve, Pedro</creatorcontrib><creatorcontrib>Dubovy, Sander R</creatorcontrib><creatorcontrib>Karp, Carol L</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Clinical ophthalmology (Auckland, N.Z.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paranjpe, Vikram</au><au>Galor, Anat</au><au>Monsalve, Pedro</au><au>Dubovy, Sander R</au><au>Karp, Carol L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Salzmann nodular degeneration: prevalence, impact, and management strategies</atitle><jtitle>Clinical ophthalmology (Auckland, N.Z.)</jtitle><addtitle>Clin Ophthalmol</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>13</volume><spage>1305</spage><epage>1314</epage><pages>1305-1314</pages><issn>1177-5467</issn><issn>1177-5483</issn><eissn>1177-5483</eissn><abstract>This review will summarize the clinical and histological presentation of Salzmann nodular degeneration (SND), its prevalence and risk factors, potential underlying mechanisms, diagnostic tools, management options, and impact on cataract surgery and co-morbid ocular surface diseases.
PubMed review of 44 articles published between 1976 and 2018.
SND is a corneal disease characterized by whitish gray or bluish nodules on the peripheral or central cornea. The clinical presentation of SND is variable and the nodules can be asymptomatic or cause foreign body sensation and/or blurred vision. Histologically, SND appears as subepithelial nodules with thin overlying epithelium, disrupted or absent Bowman's layer, and activated fibroblasts within the nodule. SND pathogenesis is not fully understood but is thought to involve poor epithelial protection and disruption of the epithelial-stromal interface, allowing for penetration of epithelially derived growth factors into the stroma and subsequent activation of stromal fibroblasts, eventually leading to sub-epithelial deposition of disorganized extracellular membrane components. SND most commonly occurs in Caucasian females in a bimodal distribution, occurring in the fifth or eighth and ninth decades of life. Risk factors for SND include ocular surface diseases and surgery. Surgical intervention is recommended in individuals with symptomatic nodules - primarily superficial keratectomy performed with or without intraoperative mitomycin C, photokeratectomy, and/or amniotic membrane transplantation. These procedures have been successful in removing the lesion and reducing corneal irregularity, but have variable recurrence rates (0-31%).
The pathogenesis of SND is complex and multifactorial. Advances in diagnostic and treatment modalities have allowed for earlier and more accurate diagnosis and effective treatment of SND.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>31413538</pmid><doi>10.2147/OPTH.S166280</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3124-2462</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cataract extraction Cataracts cornea diagnosis Ecosystems Epidemiology Epithelium Eye diseases Eye surgery imaging Lasers Microscopy Mitomycin Ophthalmology Prostheses Review Salzmann nodular degeneration Strategic planning (Business) Surgery Therapeutics Tomography Topography treatment |
title | Salzmann nodular degeneration: prevalence, impact, and management strategies |
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