Complete bilateral Tessier’s facial cleft number 5: surgical strategy for a rare case report
The oro-ocular cleft number 5 according to the Tessier classification is one of the rarest facial clefts and few cases have been reported in the literature. Although the detailed structure of rare craniofacial clefts is well established, the cause of these pathological conditions is not. There are n...
Gespeichert in:
| Veröffentlicht in: | Surgical and radiologic anatomy (English ed.) 2019-05, Vol.41 (5), p.569-574 |
|---|---|
| Hauptverfasser: | , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 574 |
|---|---|
| container_issue | 5 |
| container_start_page | 569 |
| container_title | Surgical and radiologic anatomy (English ed.) |
| container_volume | 41 |
| creator | Binet, Aurélien de Buys Roessingh, A. Hamedani, M. El Ezzi, O. |
| description | The oro-ocular cleft number 5 according to the Tessier classification is one of the rarest facial clefts and few cases have been reported in the literature. Although the detailed structure of rare craniofacial clefts is well established, the cause of these pathological conditions is not. There are no existing guidelines for the management of this particular kind of cleft. We describe the case of a 19-month-old girl with a complete bilateral facial cleft. We describe the surgical steps taken to achieve the primary correction of the soft tissue deformation. Embryologic development and radiological approach are discussed, as are also the psychological and social aspects of severe facial deformities. |
| doi_str_mv | 10.1007/s00276-019-02185-z |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2179414830</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2179414830</sourcerecordid><originalsourceid>FETCH-LOGICAL-c326t-36630bc273041acb1f583283b3ed9ca844ab24347b333d59e5e827ec4643a7b3</originalsourceid><addsrcrecordid>eNp9kMGO0zAQhi3EipaFF-CALHHhkmXscWKH26oCdqVKXHrGctxJlVXSlHFyaE-8Bq-3T4KXLiDtgZOlme__PfqEeKPgSgHYDwlA26oAVReglSuL0zOxVNrWhSuVfS6WUCMUCtAtxMuU7gCgVMq9EAuEqqyMskvxbTUOh54mkk3Xh4k49HJDKXXE9z9-JtmG2OVR7Kmd5H4eGmJZfpRp5l0X8yJNnFO7o2xHlkFyYJIxJJJMh5GnV-KiDX2i14_vpdh8_rRZ3RTrr19uV9frIqKupgKrCqGJ2iIYFWKj2tKhdtggbesYnDGh0QaNbRBxW9ZUktOWoqkMhjy8FO_PtQcev8-UJj90KVLfhz2Nc_Ja2doo4xAy-u4JejfOvM_HZapyoMCgzZQ-U5HHlJhaf-BuCHz0CvyDfH-W77N8_1u-P-XQ28fquRlo-zfyx3YG8AykvNrviP_9_Z_aX1eYj7s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2168010437</pqid></control><display><type>article</type><title>Complete bilateral Tessier’s facial cleft number 5: surgical strategy for a rare case report</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Binet, Aurélien ; de Buys Roessingh, A. ; Hamedani, M. ; El Ezzi, O.</creator><creatorcontrib>Binet, Aurélien ; de Buys Roessingh, A. ; Hamedani, M. ; El Ezzi, O.</creatorcontrib><description>The oro-ocular cleft number 5 according to the Tessier classification is one of the rarest facial clefts and few cases have been reported in the literature. Although the detailed structure of rare craniofacial clefts is well established, the cause of these pathological conditions is not. There are no existing guidelines for the management of this particular kind of cleft. We describe the case of a 19-month-old girl with a complete bilateral facial cleft. We describe the surgical steps taken to achieve the primary correction of the soft tissue deformation. Embryologic development and radiological approach are discussed, as are also the psychological and social aspects of severe facial deformities.</description><identifier>ISSN: 0930-1038</identifier><identifier>EISSN: 1279-8517</identifier><identifier>DOI: 10.1007/s00276-019-02185-z</identifier><identifier>PMID: 30656417</identifier><language>eng</language><publisher>Paris: Springer Paris</publisher><subject>Anatomy ; Case reports ; Cleft Palate - diagnostic imaging ; Cleft Palate - surgery ; Eye Abnormalities - diagnostic imaging ; Eye Abnormalities - surgery ; Face - abnormalities ; Facial Bones - abnormalities ; Facial Bones - diagnostic imaging ; Facial Bones - surgery ; Female ; Humans ; Imaging ; Infant ; Medicine ; Medicine & Public Health ; Mouth Abnormalities - diagnostic imaging ; Mouth Abnormalities - surgery ; Original Article ; Orthopedics ; Radiology ; Social factors ; Surgery ; Tomography, X-Ray Computed</subject><ispartof>Surgical and radiologic anatomy (English ed.), 2019-05, Vol.41 (5), p.569-574</ispartof><rights>Springer-Verlag France SAS, part of Springer Nature 2019</rights><rights>Surgical and Radiologic Anatomy is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c326t-36630bc273041acb1f583283b3ed9ca844ab24347b333d59e5e827ec4643a7b3</cites><orcidid>0000-0002-4378-0583</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00276-019-02185-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00276-019-02185-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30656417$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Binet, Aurélien</creatorcontrib><creatorcontrib>de Buys Roessingh, A.</creatorcontrib><creatorcontrib>Hamedani, M.</creatorcontrib><creatorcontrib>El Ezzi, O.</creatorcontrib><title>Complete bilateral Tessier’s facial cleft number 5: surgical strategy for a rare case report</title><title>Surgical and radiologic anatomy (English ed.)</title><addtitle>Surg Radiol Anat</addtitle><addtitle>Surg Radiol Anat</addtitle><description>The oro-ocular cleft number 5 according to the Tessier classification is one of the rarest facial clefts and few cases have been reported in the literature. Although the detailed structure of rare craniofacial clefts is well established, the cause of these pathological conditions is not. There are no existing guidelines for the management of this particular kind of cleft. We describe the case of a 19-month-old girl with a complete bilateral facial cleft. We describe the surgical steps taken to achieve the primary correction of the soft tissue deformation. Embryologic development and radiological approach are discussed, as are also the psychological and social aspects of severe facial deformities.</description><subject>Anatomy</subject><subject>Case reports</subject><subject>Cleft Palate - diagnostic imaging</subject><subject>Cleft Palate - surgery</subject><subject>Eye Abnormalities - diagnostic imaging</subject><subject>Eye Abnormalities - surgery</subject><subject>Face - abnormalities</subject><subject>Facial Bones - abnormalities</subject><subject>Facial Bones - diagnostic imaging</subject><subject>Facial Bones - surgery</subject><subject>Female</subject><subject>Humans</subject><subject>Imaging</subject><subject>Infant</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mouth Abnormalities - diagnostic imaging</subject><subject>Mouth Abnormalities - surgery</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Radiology</subject><subject>Social factors</subject><subject>Surgery</subject><subject>Tomography, X-Ray Computed</subject><issn>0930-1038</issn><issn>1279-8517</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMGO0zAQhi3EipaFF-CALHHhkmXscWKH26oCdqVKXHrGctxJlVXSlHFyaE-8Bq-3T4KXLiDtgZOlme__PfqEeKPgSgHYDwlA26oAVReglSuL0zOxVNrWhSuVfS6WUCMUCtAtxMuU7gCgVMq9EAuEqqyMskvxbTUOh54mkk3Xh4k49HJDKXXE9z9-JtmG2OVR7Kmd5H4eGmJZfpRp5l0X8yJNnFO7o2xHlkFyYJIxJJJMh5GnV-KiDX2i14_vpdh8_rRZ3RTrr19uV9frIqKupgKrCqGJ2iIYFWKj2tKhdtggbesYnDGh0QaNbRBxW9ZUktOWoqkMhjy8FO_PtQcev8-UJj90KVLfhz2Nc_Ja2doo4xAy-u4JejfOvM_HZapyoMCgzZQ-U5HHlJhaf-BuCHz0CvyDfH-W77N8_1u-P-XQ28fquRlo-zfyx3YG8AykvNrviP_9_Z_aX1eYj7s</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Binet, Aurélien</creator><creator>de Buys Roessingh, A.</creator><creator>Hamedani, M.</creator><creator>El Ezzi, O.</creator><general>Springer Paris</general><general>Springer Nature B.V</general><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>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4378-0583</orcidid></search><sort><creationdate>20190501</creationdate><title>Complete bilateral Tessier’s facial cleft number 5: surgical strategy for a rare case report</title><author>Binet, Aurélien ; de Buys Roessingh, A. ; Hamedani, M. ; El Ezzi, O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-36630bc273041acb1f583283b3ed9ca844ab24347b333d59e5e827ec4643a7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anatomy</topic><topic>Case reports</topic><topic>Cleft Palate - diagnostic imaging</topic><topic>Cleft Palate - surgery</topic><topic>Eye Abnormalities - diagnostic imaging</topic><topic>Eye Abnormalities - surgery</topic><topic>Face - abnormalities</topic><topic>Facial Bones - abnormalities</topic><topic>Facial Bones - diagnostic imaging</topic><topic>Facial Bones - surgery</topic><topic>Female</topic><topic>Humans</topic><topic>Imaging</topic><topic>Infant</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mouth Abnormalities - diagnostic imaging</topic><topic>Mouth Abnormalities - surgery</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Radiology</topic><topic>Social factors</topic><topic>Surgery</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Binet, Aurélien</creatorcontrib><creatorcontrib>de Buys Roessingh, A.</creatorcontrib><creatorcontrib>Hamedani, M.</creatorcontrib><creatorcontrib>El Ezzi, O.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Surgical and radiologic anatomy (English ed.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Binet, Aurélien</au><au>de Buys Roessingh, A.</au><au>Hamedani, M.</au><au>El Ezzi, O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complete bilateral Tessier’s facial cleft number 5: surgical strategy for a rare case report</atitle><jtitle>Surgical and radiologic anatomy (English ed.)</jtitle><stitle>Surg Radiol Anat</stitle><addtitle>Surg Radiol Anat</addtitle><date>2019-05-01</date><risdate>2019</risdate><volume>41</volume><issue>5</issue><spage>569</spage><epage>574</epage><pages>569-574</pages><issn>0930-1038</issn><eissn>1279-8517</eissn><abstract>The oro-ocular cleft number 5 according to the Tessier classification is one of the rarest facial clefts and few cases have been reported in the literature. Although the detailed structure of rare craniofacial clefts is well established, the cause of these pathological conditions is not. There are no existing guidelines for the management of this particular kind of cleft. We describe the case of a 19-month-old girl with a complete bilateral facial cleft. We describe the surgical steps taken to achieve the primary correction of the soft tissue deformation. Embryologic development and radiological approach are discussed, as are also the psychological and social aspects of severe facial deformities.</abstract><cop>Paris</cop><pub>Springer Paris</pub><pmid>30656417</pmid><doi>10.1007/s00276-019-02185-z</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-4378-0583</orcidid></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0930-1038 |
| ispartof | Surgical and radiologic anatomy (English ed.), 2019-05, Vol.41 (5), p.569-574 |
| issn | 0930-1038 1279-8517 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_2179414830 |
| source | MEDLINE; SpringerLink Journals - AutoHoldings |
| subjects | Anatomy Case reports Cleft Palate - diagnostic imaging Cleft Palate - surgery Eye Abnormalities - diagnostic imaging Eye Abnormalities - surgery Face - abnormalities Facial Bones - abnormalities Facial Bones - diagnostic imaging Facial Bones - surgery Female Humans Imaging Infant Medicine Medicine & Public Health Mouth Abnormalities - diagnostic imaging Mouth Abnormalities - surgery Original Article Orthopedics Radiology Social factors Surgery Tomography, X-Ray Computed |
| title | Complete bilateral Tessier’s facial cleft number 5: surgical strategy for a rare case report |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T12%3A36%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Complete%20bilateral%20Tessier%E2%80%99s%20facial%20cleft%20number%205:%20surgical%20strategy%20for%20a%20rare%20case%20report&rft.jtitle=Surgical%20and%20radiologic%20anatomy%20(English%20ed.)&rft.au=Binet,%20Aur%C3%A9lien&rft.date=2019-05-01&rft.volume=41&rft.issue=5&rft.spage=569&rft.epage=574&rft.pages=569-574&rft.issn=0930-1038&rft.eissn=1279-8517&rft_id=info:doi/10.1007/s00276-019-02185-z&rft_dat=%3Cproquest_cross%3E2179414830%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2168010437&rft_id=info:pmid/30656417&rfr_iscdi=true |