Primary orbital angiosarcoma : A case report
The pathogenesis, natural history, histopathology, and recommended treatment for orbital angiosarcoma are illustrated and reviewed. Case report. A 71-year-old white male presented with bluish discoloration and swelling of the left medial canthal area. A fine needle aspiration and excisional biopsy w...
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| Veröffentlicht in: | Ophthalmic plastic and reconstructive surgery 1999-11, Vol.15 (6), p.454-459 |
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| container_title | Ophthalmic plastic and reconstructive surgery |
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| creator | SIDDENS, J. D FISHMAN, J. R. A JACKSON, I. T NESI, F. A TSAO, K |
| description | The pathogenesis, natural history, histopathology, and recommended treatment for orbital angiosarcoma are illustrated and reviewed.
Case report.
A 71-year-old white male presented with bluish discoloration and swelling of the left medial canthal area. A fine needle aspiration and excisional biopsy with histopathologic examination was performed, which showed angiosarcoma. Pattern of growth was demonstrated radiographically and histopathologically, confirming primary orbital angiosarcoma. Subsequent wide surgical resection was carried out, with substantial reconstruction of the left orbital and periorbital area. The patient responded well to the surgery, and was free of tumor after six years of follow-up.
Angiosarcoma is a rare and highly malignant tumor of epithelial origin. The aggressive nature of this tumor usually results in a high mortality rate despite treatment. However, early diagnosis and wide surgical excision has resulted in successful treatment of these tumors. |
| doi_str_mv | 10.1097/00002341-199911000-00019 |
| format | Article |
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Case report.
A 71-year-old white male presented with bluish discoloration and swelling of the left medial canthal area. A fine needle aspiration and excisional biopsy with histopathologic examination was performed, which showed angiosarcoma. Pattern of growth was demonstrated radiographically and histopathologically, confirming primary orbital angiosarcoma. Subsequent wide surgical resection was carried out, with substantial reconstruction of the left orbital and periorbital area. The patient responded well to the surgery, and was free of tumor after six years of follow-up.
Angiosarcoma is a rare and highly malignant tumor of epithelial origin. The aggressive nature of this tumor usually results in a high mortality rate despite treatment. However, early diagnosis and wide surgical excision has resulted in successful treatment of these tumors.</description><identifier>ISSN: 0740-9303</identifier><identifier>EISSN: 1537-2677</identifier><identifier>DOI: 10.1097/00002341-199911000-00019</identifier><identifier>PMID: 10588260</identifier><identifier>CODEN: OPRSEU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams and Wilkins</publisher><subject>Aged ; Biological and medical sciences ; Biopsy ; Hemangiosarcoma - diagnostic imaging ; Hemangiosarcoma - pathology ; Hemangiosarcoma - surgery ; Humans ; Male ; Medical sciences ; Ophthalmology ; Orbit Evisceration ; Orbital Neoplasms - diagnostic imaging ; Orbital Neoplasms - pathology ; Orbital Neoplasms - surgery ; Tomography, X-Ray Computed ; Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus</subject><ispartof>Ophthalmic plastic and reconstructive surgery, 1999-11, Vol.15 (6), p.454-459</ispartof><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1201095$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10588260$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SIDDENS, J. D</creatorcontrib><creatorcontrib>FISHMAN, J. R. A</creatorcontrib><creatorcontrib>JACKSON, I. T</creatorcontrib><creatorcontrib>NESI, F. A</creatorcontrib><creatorcontrib>TSAO, K</creatorcontrib><title>Primary orbital angiosarcoma : A case report</title><title>Ophthalmic plastic and reconstructive surgery</title><addtitle>Ophthalmic Plast Reconstr Surg</addtitle><description>The pathogenesis, natural history, histopathology, and recommended treatment for orbital angiosarcoma are illustrated and reviewed.
Case report.
A 71-year-old white male presented with bluish discoloration and swelling of the left medial canthal area. A fine needle aspiration and excisional biopsy with histopathologic examination was performed, which showed angiosarcoma. Pattern of growth was demonstrated radiographically and histopathologically, confirming primary orbital angiosarcoma. Subsequent wide surgical resection was carried out, with substantial reconstruction of the left orbital and periorbital area. The patient responded well to the surgery, and was free of tumor after six years of follow-up.
Angiosarcoma is a rare and highly malignant tumor of epithelial origin. The aggressive nature of this tumor usually results in a high mortality rate despite treatment. However, early diagnosis and wide surgical excision has resulted in successful treatment of these tumors.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Hemangiosarcoma - diagnostic imaging</subject><subject>Hemangiosarcoma - pathology</subject><subject>Hemangiosarcoma - surgery</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Ophthalmology</subject><subject>Orbit Evisceration</subject><subject>Orbital Neoplasms - diagnostic imaging</subject><subject>Orbital Neoplasms - pathology</subject><subject>Orbital Neoplasms - surgery</subject><subject>Tomography, X-Ray Computed</subject><subject>Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus</subject><issn>0740-9303</issn><issn>1537-2677</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE1LAzEQhoMotlb_guxBPBmdJJvNxlspfkFBD3oO02wiK7tNTbYH_73RrR-BEAaeNzPzEFIwuGSg1RXkw0XJKNNaM5Yrmi_Te2TKpFCUV0rtkymoEqgWICbkKKW3TCgh5SGZMJB1zSuYkoun2PYYP4oQV-2AXYHr1zYkjDb0WFwX88JickV0mxCHY3LgsUvuZPfOyMvtzfPini4f7x4W8yW1vJYDZV5araEUDErelJWGRoJQUot6VQN6JQHRWYtVmedgnsvGq0o5zVyZQ07MyPn47yaG961Lg-nbZF3X4dqFbTKVFoILJTJYj6CNIaXovNmM6xgG5suU-TFlfk2Zb1M5errrsV31rvkXHNVk4GwHYLLY-Yhr26Y_jkNuIMUn2hBtgw</recordid><startdate>19991101</startdate><enddate>19991101</enddate><creator>SIDDENS, J. D</creator><creator>FISHMAN, J. R. A</creator><creator>JACKSON, I. T</creator><creator>NESI, F. A</creator><creator>TSAO, K</creator><general>Lippincott Williams and Wilkins</general><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>7X8</scope></search><sort><creationdate>19991101</creationdate><title>Primary orbital angiosarcoma : A case report</title><author>SIDDENS, J. D ; FISHMAN, J. R. A ; JACKSON, I. T ; NESI, F. A ; TSAO, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c285t-1f5c990431042d4690d50375938b80af750aaecca640581f25df767e91e4431e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Hemangiosarcoma - diagnostic imaging</topic><topic>Hemangiosarcoma - pathology</topic><topic>Hemangiosarcoma - surgery</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Ophthalmology</topic><topic>Orbit Evisceration</topic><topic>Orbital Neoplasms - diagnostic imaging</topic><topic>Orbital Neoplasms - pathology</topic><topic>Orbital Neoplasms - surgery</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>SIDDENS, J. D</creatorcontrib><creatorcontrib>FISHMAN, J. R. A</creatorcontrib><creatorcontrib>JACKSON, I. T</creatorcontrib><creatorcontrib>NESI, F. A</creatorcontrib><creatorcontrib>TSAO, K</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Ophthalmic plastic and reconstructive surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SIDDENS, J. D</au><au>FISHMAN, J. R. A</au><au>JACKSON, I. T</au><au>NESI, F. A</au><au>TSAO, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary orbital angiosarcoma : A case report</atitle><jtitle>Ophthalmic plastic and reconstructive surgery</jtitle><addtitle>Ophthalmic Plast Reconstr Surg</addtitle><date>1999-11-01</date><risdate>1999</risdate><volume>15</volume><issue>6</issue><spage>454</spage><epage>459</epage><pages>454-459</pages><issn>0740-9303</issn><eissn>1537-2677</eissn><coden>OPRSEU</coden><abstract>The pathogenesis, natural history, histopathology, and recommended treatment for orbital angiosarcoma are illustrated and reviewed.
Case report.
A 71-year-old white male presented with bluish discoloration and swelling of the left medial canthal area. A fine needle aspiration and excisional biopsy with histopathologic examination was performed, which showed angiosarcoma. Pattern of growth was demonstrated radiographically and histopathologically, confirming primary orbital angiosarcoma. Subsequent wide surgical resection was carried out, with substantial reconstruction of the left orbital and periorbital area. The patient responded well to the surgery, and was free of tumor after six years of follow-up.
Angiosarcoma is a rare and highly malignant tumor of epithelial origin. The aggressive nature of this tumor usually results in a high mortality rate despite treatment. However, early diagnosis and wide surgical excision has resulted in successful treatment of these tumors.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams and Wilkins</pub><pmid>10588260</pmid><doi>10.1097/00002341-199911000-00019</doi><tpages>6</tpages></addata></record> |
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| ispartof | Ophthalmic plastic and reconstructive surgery, 1999-11, Vol.15 (6), p.454-459 |
| issn | 0740-9303 1537-2677 |
| language | eng |
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| source | Journals@Ovid Ovid Autoload; MEDLINE |
| subjects | Aged Biological and medical sciences Biopsy Hemangiosarcoma - diagnostic imaging Hemangiosarcoma - pathology Hemangiosarcoma - surgery Humans Male Medical sciences Ophthalmology Orbit Evisceration Orbital Neoplasms - diagnostic imaging Orbital Neoplasms - pathology Orbital Neoplasms - surgery Tomography, X-Ray Computed Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus |
| title | Primary orbital angiosarcoma : A case report |
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