Retinoblastoma associated orbital cellulitis
AIM Preseptal and orbital cellulitis are rare presenting features of intraocular retinoblastoma. The objectives of this study were to determine the frequency of retinoblastoma associated cellulitis, as well as to review its clinical and histopathological features. METHODS The medical records of 292...
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Veröffentlicht in: | British journal of ophthalmology 1998-05, Vol.82 (5), p.517-521 |
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description | AIM Preseptal and orbital cellulitis are rare presenting features of intraocular retinoblastoma. The objectives of this study were to determine the frequency of retinoblastoma associated cellulitis, as well as to review its clinical and histopathological features. METHODS The medical records of 292 retinoblastoma patients in the King Khaled Eye Specialist Hospital in Riyadh, Saudi Arabia were reviewed. Those indicating a history of, or presenting with, cellulitis were retrieved and their clinical, radiological, and histopathological variables were assessed. Patients with definite extraocular tumour extension on clinical or radiological examination were excluded. RESULTS 14 patients were found to have retinoblastoma associated cellulitis (4.8%); nine had bilateral and five had unilateral retinoblastoma. Conjunctival and blood cultures were performed in 10 cases and were negative. 10 children were treated with intravenous steroids, often in conjunction with antibiotics, resulting in a prompt decrease in inflammation. Three other children were treated with antibiotics alone and one received no treatment. Computed tomographic scanning depicted large intraocular tumours occupying between 80% and 100% of the globe in each case. In eight patients, periocular inflammation was radiologically interpreted as possible extraocular extension. In one patient serial computed tomographic scanning showed a reduction in intraocular calcification over time which occurred in the presence of cellulitis. 12 patients underwent enucleation and histopathological examination revealed large necrotic, poorly differentiated tumours associated with uveal involvement and early optic nerve invasion. Focal perilimbal destruction was seen in one patient, and in another peripapillary extrascleral extension was present. 12 patients are alive with a mean follow up of 56.4 months. CONCLUSIONS Radiological evaluation of scleral integrity may be hindered by periocular inflammatory changes. The orbital cellulitis correlated well with the presence of advanced intraocular retinoblastoma with massive necrosis and anterior chamber involvement. In the majority of patients, cellulitis was not indicative of an extension of retinoblastoma into the orbit. Intravenous steroid treatment reduced orbital inflammation, facilitating examination and subsequent enucleation. |
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The objectives of this study were to determine the frequency of retinoblastoma associated cellulitis, as well as to review its clinical and histopathological features. METHODS The medical records of 292 retinoblastoma patients in the King Khaled Eye Specialist Hospital in Riyadh, Saudi Arabia were reviewed. Those indicating a history of, or presenting with, cellulitis were retrieved and their clinical, radiological, and histopathological variables were assessed. Patients with definite extraocular tumour extension on clinical or radiological examination were excluded. RESULTS 14 patients were found to have retinoblastoma associated cellulitis (4.8%); nine had bilateral and five had unilateral retinoblastoma. Conjunctival and blood cultures were performed in 10 cases and were negative. 10 children were treated with intravenous steroids, often in conjunction with antibiotics, resulting in a prompt decrease in inflammation. Three other children were treated with antibiotics alone and one received no treatment. Computed tomographic scanning depicted large intraocular tumours occupying between 80% and 100% of the globe in each case. In eight patients, periocular inflammation was radiologically interpreted as possible extraocular extension. In one patient serial computed tomographic scanning showed a reduction in intraocular calcification over time which occurred in the presence of cellulitis. 12 patients underwent enucleation and histopathological examination revealed large necrotic, poorly differentiated tumours associated with uveal involvement and early optic nerve invasion. Focal perilimbal destruction was seen in one patient, and in another peripapillary extrascleral extension was present. 12 patients are alive with a mean follow up of 56.4 months. CONCLUSIONS Radiological evaluation of scleral integrity may be hindered by periocular inflammatory changes. The orbital cellulitis correlated well with the presence of advanced intraocular retinoblastoma with massive necrosis and anterior chamber involvement. In the majority of patients, cellulitis was not indicative of an extension of retinoblastoma into the orbit. Intravenous steroid treatment reduced orbital inflammation, facilitating examination and subsequent enucleation.</description><identifier>ISSN: 0007-1161</identifier><identifier>EISSN: 1468-2079</identifier><identifier>DOI: 10.1136/bjo.82.5.517</identifier><identifier>PMID: 9713058</identifier><identifier>CODEN: BJOPAL</identifier><language>eng</language><publisher>BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group Ltd</publisher><subject>Biological and medical sciences ; Cellulitis - diagnostic imaging ; Cellulitis - etiology ; Child, Preschool ; Female ; Humans ; Infant ; Male ; Medical sciences ; Ophthalmology ; orbital cellulitis ; Orbital Diseases - diagnostic imaging ; Orbital Diseases - etiology ; Original articles - Clinical science ; Paraneoplastic Syndromes - diagnostic imaging ; Paraneoplastic Syndromes - etiology ; Retinal Neoplasms - complications ; Retinal Neoplasms - diagnostic imaging ; Retinal Neoplasms - pathology ; retinoblastoma ; Retinoblastoma - complications ; Retinoblastoma - diagnostic imaging ; Retinoblastoma - pathology ; Tomography, X-Ray Computed ; Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus</subject><ispartof>British journal of ophthalmology, 1998-05, Vol.82 (5), p.517-521</ispartof><rights>British Journal of Ophthalmology</rights><rights>1998 INIST-CNRS</rights><rights>Copyright: 1998 British Journal of Ophthalmology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b506t-c44f7a8fd0ad6b5a2fa36428c46576bf6f2fd2e64199a3419931981605b9d3593</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1722581/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1722581/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2244310$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9713058$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mullaney, Paul B</creatorcontrib><creatorcontrib>Karcioglu, Zeynel A</creatorcontrib><creatorcontrib>Huaman, Antonio M</creatorcontrib><creatorcontrib>Al-Mesfer, Saleh</creatorcontrib><title>Retinoblastoma associated orbital cellulitis</title><title>British journal of ophthalmology</title><addtitle>Br J Ophthalmol</addtitle><description>AIM Preseptal and orbital cellulitis are rare presenting features of intraocular retinoblastoma. The objectives of this study were to determine the frequency of retinoblastoma associated cellulitis, as well as to review its clinical and histopathological features. METHODS The medical records of 292 retinoblastoma patients in the King Khaled Eye Specialist Hospital in Riyadh, Saudi Arabia were reviewed. Those indicating a history of, or presenting with, cellulitis were retrieved and their clinical, radiological, and histopathological variables were assessed. Patients with definite extraocular tumour extension on clinical or radiological examination were excluded. RESULTS 14 patients were found to have retinoblastoma associated cellulitis (4.8%); nine had bilateral and five had unilateral retinoblastoma. Conjunctival and blood cultures were performed in 10 cases and were negative. 10 children were treated with intravenous steroids, often in conjunction with antibiotics, resulting in a prompt decrease in inflammation. Three other children were treated with antibiotics alone and one received no treatment. Computed tomographic scanning depicted large intraocular tumours occupying between 80% and 100% of the globe in each case. In eight patients, periocular inflammation was radiologically interpreted as possible extraocular extension. In one patient serial computed tomographic scanning showed a reduction in intraocular calcification over time which occurred in the presence of cellulitis. 12 patients underwent enucleation and histopathological examination revealed large necrotic, poorly differentiated tumours associated with uveal involvement and early optic nerve invasion. Focal perilimbal destruction was seen in one patient, and in another peripapillary extrascleral extension was present. 12 patients are alive with a mean follow up of 56.4 months. CONCLUSIONS Radiological evaluation of scleral integrity may be hindered by periocular inflammatory changes. The orbital cellulitis correlated well with the presence of advanced intraocular retinoblastoma with massive necrosis and anterior chamber involvement. In the majority of patients, cellulitis was not indicative of an extension of retinoblastoma into the orbit. Intravenous steroid treatment reduced orbital inflammation, facilitating examination and subsequent enucleation.</description><subject>Biological and medical sciences</subject><subject>Cellulitis - diagnostic imaging</subject><subject>Cellulitis - etiology</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Ophthalmology</subject><subject>orbital cellulitis</subject><subject>Orbital Diseases - diagnostic imaging</subject><subject>Orbital Diseases - etiology</subject><subject>Original articles - Clinical science</subject><subject>Paraneoplastic Syndromes - diagnostic imaging</subject><subject>Paraneoplastic Syndromes - etiology</subject><subject>Retinal Neoplasms - complications</subject><subject>Retinal Neoplasms - diagnostic imaging</subject><subject>Retinal Neoplasms - pathology</subject><subject>retinoblastoma</subject><subject>Retinoblastoma - complications</subject><subject>Retinoblastoma - diagnostic imaging</subject><subject>Retinoblastoma - pathology</subject><subject>Tomography, X-Ray Computed</subject><subject>Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus</subject><issn>0007-1161</issn><issn>1468-2079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kd1rFDEUxYNY6lp981VYUOpLZ5vvZF4EWbRVFgtFfQ03M4lmnZnUJFP0vzfLLov64MsNl_PjcG4OQs8IXhHC5KXdxpWmK7ESRD1AC8KlbihW7UO0wBirhhBJHqHHOW_rSiVRp-i0VYRhoRfo4taVMEU7QC5xhCXkHLsAxfXLmGwoMCw7NwzzEErIT9CJhyG7p4f3DH1-9_bT-rrZ3Fy9X7_ZNFZgWZqOc69A-x5DL60A6oFJTnXHpVDSeump76mTnLQtsN1kpNVEYmHbnomWnaHXe9-72Y6u79xUEgzmLoUR0i8TIZi_lSl8M1_jvSGKUqFJNTg_GKT4Y3a5mDHk3R0wuThno5jmSjNZwRf_gNs4p6keV72UbiVVmFXqYk91KeacnD9GIdjsOjC1A6OpEaZ2UPHnf8Y_wodPr_rLgw65g8EnmLqQjxilnDOCK9bssZCL-3mUIX03UjElzMcva7MmH_gGX3FzW_lXe96O2_8H_A0oJ6nM</recordid><startdate>19980501</startdate><enddate>19980501</enddate><creator>Mullaney, Paul B</creator><creator>Karcioglu, Zeynel A</creator><creator>Huaman, Antonio M</creator><creator>Al-Mesfer, Saleh</creator><general>BMJ Publishing Group Ltd</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19980501</creationdate><title>Retinoblastoma associated orbital cellulitis</title><author>Mullaney, Paul B ; Karcioglu, Zeynel A ; Huaman, Antonio M ; Al-Mesfer, Saleh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b506t-c44f7a8fd0ad6b5a2fa36428c46576bf6f2fd2e64199a3419931981605b9d3593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Biological and medical sciences</topic><topic>Cellulitis - diagnostic imaging</topic><topic>Cellulitis - etiology</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Ophthalmology</topic><topic>orbital cellulitis</topic><topic>Orbital Diseases - diagnostic imaging</topic><topic>Orbital Diseases - etiology</topic><topic>Original articles - Clinical science</topic><topic>Paraneoplastic Syndromes - diagnostic imaging</topic><topic>Paraneoplastic Syndromes - etiology</topic><topic>Retinal Neoplasms - complications</topic><topic>Retinal Neoplasms - diagnostic imaging</topic><topic>Retinal Neoplasms - pathology</topic><topic>retinoblastoma</topic><topic>Retinoblastoma - complications</topic><topic>Retinoblastoma - diagnostic imaging</topic><topic>Retinoblastoma - pathology</topic><topic>Tomography, X-Ray Computed</topic><topic>Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mullaney, Paul B</creatorcontrib><creatorcontrib>Karcioglu, Zeynel A</creatorcontrib><creatorcontrib>Huaman, Antonio M</creatorcontrib><creatorcontrib>Al-Mesfer, Saleh</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><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>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mullaney, Paul B</au><au>Karcioglu, Zeynel A</au><au>Huaman, Antonio M</au><au>Al-Mesfer, Saleh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retinoblastoma associated orbital cellulitis</atitle><jtitle>British journal of ophthalmology</jtitle><addtitle>Br J Ophthalmol</addtitle><date>1998-05-01</date><risdate>1998</risdate><volume>82</volume><issue>5</issue><spage>517</spage><epage>521</epage><pages>517-521</pages><issn>0007-1161</issn><eissn>1468-2079</eissn><coden>BJOPAL</coden><abstract>AIM Preseptal and orbital cellulitis are rare presenting features of intraocular retinoblastoma. The objectives of this study were to determine the frequency of retinoblastoma associated cellulitis, as well as to review its clinical and histopathological features. METHODS The medical records of 292 retinoblastoma patients in the King Khaled Eye Specialist Hospital in Riyadh, Saudi Arabia were reviewed. Those indicating a history of, or presenting with, cellulitis were retrieved and their clinical, radiological, and histopathological variables were assessed. Patients with definite extraocular tumour extension on clinical or radiological examination were excluded. RESULTS 14 patients were found to have retinoblastoma associated cellulitis (4.8%); nine had bilateral and five had unilateral retinoblastoma. Conjunctival and blood cultures were performed in 10 cases and were negative. 10 children were treated with intravenous steroids, often in conjunction with antibiotics, resulting in a prompt decrease in inflammation. Three other children were treated with antibiotics alone and one received no treatment. Computed tomographic scanning depicted large intraocular tumours occupying between 80% and 100% of the globe in each case. In eight patients, periocular inflammation was radiologically interpreted as possible extraocular extension. In one patient serial computed tomographic scanning showed a reduction in intraocular calcification over time which occurred in the presence of cellulitis. 12 patients underwent enucleation and histopathological examination revealed large necrotic, poorly differentiated tumours associated with uveal involvement and early optic nerve invasion. Focal perilimbal destruction was seen in one patient, and in another peripapillary extrascleral extension was present. 12 patients are alive with a mean follow up of 56.4 months. CONCLUSIONS Radiological evaluation of scleral integrity may be hindered by periocular inflammatory changes. The orbital cellulitis correlated well with the presence of advanced intraocular retinoblastoma with massive necrosis and anterior chamber involvement. In the majority of patients, cellulitis was not indicative of an extension of retinoblastoma into the orbit. Intravenous steroid treatment reduced orbital inflammation, facilitating examination and subsequent enucleation.</abstract><cop>BMA House, Tavistock Square, London, WC1H 9JR</cop><pub>BMJ Publishing Group Ltd</pub><pmid>9713058</pmid><doi>10.1136/bjo.82.5.517</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Cellulitis - diagnostic imaging Cellulitis - etiology Child, Preschool Female Humans Infant Male Medical sciences Ophthalmology orbital cellulitis Orbital Diseases - diagnostic imaging Orbital Diseases - etiology Original articles - Clinical science Paraneoplastic Syndromes - diagnostic imaging Paraneoplastic Syndromes - etiology Retinal Neoplasms - complications Retinal Neoplasms - diagnostic imaging Retinal Neoplasms - pathology retinoblastoma Retinoblastoma - complications Retinoblastoma - diagnostic imaging Retinoblastoma - pathology Tomography, X-Ray Computed Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus |
title | Retinoblastoma associated orbital cellulitis |
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