Congenital Palatal Fistula Associated with Submucous Cleft Palate
BACKGROUND:Although cleft lip and cleft palate are among the most common congenital malformations, the presence of an isolated congenital palatal fistula along with a submucous cleft is very rare. This appears as an oval-shaped, full-thickness fenestration in the palatal midline that does not fully...
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Published in: | Plastic and reconstructive surgery. Global open Vol. 4; no. 2; p. e613 |
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American Society of Plastic Surgeons
01-02-2016
Wolters Kluwer Health |
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Abstract | BACKGROUND:Although cleft lip and cleft palate are among the most common congenital malformations, the presence of an isolated congenital palatal fistula along with a submucous cleft is very rare. This appears as an oval-shaped, full-thickness fenestration in the palatal midline that does not fully extend anteriorly or posteriorly, accompanied by the findings of a submucous cleft. Because of the uncommon nature of this entity, there is controversy about its etiology, diagnosis, and management.
METHODS:Two cases of children with congenital palatal fistulae and a submucous cleft palate are presented who were treated in different settings by different surgeons. Cases are discussed along with a thorough review of the available literature.
RESULTS:Patient 1 presented at 4 years of age with “a hole in the palate” since birth and abnormal speech. His palatal fistula and submucous cleft were repaired with a modified von Langenbeck technique in Ethiopia. At a 2-year follow-up, the palate remained closed, but hypernasal speech persisted. Patient 2 was a 1-year-old presenting with failure to thrive and nasal regurgitation, who underwent a Furlow palatoplasty in the United States with good immediate results. She was unfortunately lost to follow-up.
CONCLUSIONS:A congenital fenestration of the palate is rare. Reports reveal suboptimal speech at follow-up, despite various types of repair, especially when combined with a submucous cleft. Available literature suggests that repair should not focus on fistula closure only but instead on providing adequate palate length to provide good velopharyngeal function, as in any cleft palate repair. |
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AbstractList | Although cleft lip and cleft palate are among the most common congenital malformations, the presence of an isolated congenital palatal fistula along with a submucous cleft is very rare. This appears as an oval-shaped, full-thickness fenestration in the palatal midline that does not fully extend anteriorly or posteriorly, accompanied by the findings of a submucous cleft. Because of the uncommon nature of this entity, there is controversy about its etiology, diagnosis, and management. BACKGROUND:Although cleft lip and cleft palate are among the most common congenital malformations, the presence of an isolated congenital palatal fistula along with a submucous cleft is very rare. This appears as an oval-shaped, full-thickness fenestration in the palatal midline that does not fully extend anteriorly or posteriorly, accompanied by the findings of a submucous cleft. Because of the uncommon nature of this entity, there is controversy about its etiology, diagnosis, and management. METHODS:Two cases of children with congenital palatal fistulae and a submucous cleft palate are presented who were treated in different settings by different surgeons. Cases are discussed along with a thorough review of the available literature. RESULTS:Patient 1 presented at 4 years of age with “a hole in the palate” since birth and abnormal speech. His palatal fistula and submucous cleft were repaired with a modified von Langenbeck technique in Ethiopia. At a 2-year follow-up, the palate remained closed, but hypernasal speech persisted. Patient 2 was a 1-year-old presenting with failure to thrive and nasal regurgitation, who underwent a Furlow palatoplasty in the United States with good immediate results. She was unfortunately lost to follow-up. CONCLUSIONS:A congenital fenestration of the palate is rare. Reports reveal suboptimal speech at follow-up, despite various types of repair, especially when combined with a submucous cleft. Available literature suggests that repair should not focus on fistula closure only but instead on providing adequate palate length to provide good velopharyngeal function, as in any cleft palate repair. Although cleft lip and cleft palate are among the most common congenital malformations, the presence of an isolated congenital palatal fistula along with a submucous cleft is very rare. This appears as an oval-shaped, full-thickness fenestration in the palatal midline that does not fully extend anteriorly or posteriorly, accompanied by the findings of a submucous cleft. Because of the uncommon nature of this entity, there is controversy about its etiology, diagnosis, and management. Two cases of children with congenital palatal fistulae and a submucous cleft palate are presented who were treated in different settings by different surgeons. Cases are discussed along with a thorough review of the available literature. Patient 1 presented at 4 years of age with "a hole in the palate" since birth and abnormal speech. His palatal fistula and submucous cleft were repaired with a modified von Langenbeck technique in Ethiopia. At a 2-year follow-up, the palate remained closed, but hypernasal speech persisted. Patient 2 was a 1-year-old presenting with failure to thrive and nasal regurgitation, who underwent a Furlow palatoplasty in the United States with good immediate results. She was unfortunately lost to follow-up. A congenital fenestration of the palate is rare. Reports reveal suboptimal speech at follow-up, despite various types of repair, especially when combined with a submucous cleft. Available literature suggests that repair should not focus on fistula closure only but instead on providing adequate palate length to provide good velopharyngeal function, as in any cleft palate repair. UNLABELLEDAlthough cleft lip and cleft palate are among the most common congenital malformations, the presence of an isolated congenital palatal fistula along with a submucous cleft is very rare. This appears as an oval-shaped, full-thickness fenestration in the palatal midline that does not fully extend anteriorly or posteriorly, accompanied by the findings of a submucous cleft. Because of the uncommon nature of this entity, there is controversy about its etiology, diagnosis, and management. METHODSTwo cases of children with congenital palatal fistulae and a submucous cleft palate are presented who were treated in different settings by different surgeons. Cases are discussed along with a thorough review of the available literature. RESULTSPatient 1 presented at 4 years of age with "a hole in the palate" since birth and abnormal speech. His palatal fistula and submucous cleft were repaired with a modified von Langenbeck technique in Ethiopia. At a 2-year follow-up, the palate remained closed, but hypernasal speech persisted. Patient 2 was a 1-year-old presenting with failure to thrive and nasal regurgitation, who underwent a Furlow palatoplasty in the United States with good immediate results. She was unfortunately lost to follow-up. CONCLUSIONSA congenital fenestration of the palate is rare. Reports reveal suboptimal speech at follow-up, despite various types of repair, especially when combined with a submucous cleft. Available literature suggests that repair should not focus on fistula closure only but instead on providing adequate palate length to provide good velopharyngeal function, as in any cleft palate repair. |
Author | Eshete, Mekonen Butali, Azeez Losken, H Wolfgang Demissie, Yohannes Spiess, Alexander M Hailu, Taye Camison, Liliana Abate, Fikre Mohammed, Ibrahim |
AuthorAffiliation | From the Department of Surgery, Faculty of Health Sciences School of Medicine, Addis Ababa University, Addis Ababa, Ethiopia; †Department of Plastic Surgery, University of Pittsburgh, Pittsburgh, Pa.; ‡Burn/Cleft Lip and Palate Unit, Yekatit 12 Hospital Medical College, Addis Ababa, Ethiopia; §Department of Oral Pathology, Radiology and Medicine, College of Dentistry, University of Iowa, Iowa City, Iowa; and ¶University of North Carolina at Chapel Hill, Chapel Hill, N.C |
AuthorAffiliation_xml | – name: From the Department of Surgery, Faculty of Health Sciences School of Medicine, Addis Ababa University, Addis Ababa, Ethiopia; †Department of Plastic Surgery, University of Pittsburgh, Pittsburgh, Pa.; ‡Burn/Cleft Lip and Palate Unit, Yekatit 12 Hospital Medical College, Addis Ababa, Ethiopia; §Department of Oral Pathology, Radiology and Medicine, College of Dentistry, University of Iowa, Iowa City, Iowa; and ¶University of North Carolina at Chapel Hill, Chapel Hill, N.C |
Author_xml | – sequence: 1 givenname: Mekonen surname: Eshete fullname: Eshete, Mekonen organization: From the Department of Surgery, Faculty of Health Sciences School of Medicine, Addis Ababa University, Addis Ababa, Ethiopia; †Department of Plastic Surgery, University of Pittsburgh, Pittsburgh, Pa.; ‡Burn/Cleft Lip and Palate Unit, Yekatit 12 Hospital Medical College, Addis Ababa, Ethiopia; §Department of Oral Pathology, Radiology and Medicine, College of Dentistry, University of Iowa, Iowa City, Iowa; and ¶University of North Carolina at Chapel Hill, Chapel Hill, N.C – sequence: 2 givenname: Liliana surname: Camison fullname: Camison, Liliana – sequence: 3 givenname: Fikre surname: Abate fullname: Abate, Fikre – sequence: 4 givenname: Taye surname: Hailu fullname: Hailu, Taye – sequence: 5 givenname: Yohannes surname: Demissie fullname: Demissie, Yohannes – sequence: 6 givenname: Ibrahim surname: Mohammed fullname: Mohammed, Ibrahim – sequence: 7 givenname: Azeez surname: Butali fullname: Butali, Azeez – sequence: 8 givenname: H surname: Losken middlename: Wolfgang fullname: Losken, H Wolfgang – sequence: 9 givenname: Alexander surname: Spiess middlename: M fullname: Spiess, Alexander M |
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Cites_doi | 10.1016/S1010-5182(98)80073-5 10.1097/00006534-196638060-00010 10.1016/S0007-1226(53)80060-3 10.1597/05-0131.1 10.1097/00006534-197210000-00015 10.1097/SCS.0b013e3181b14722 10.4103/2229-516X.140745 10.1016/j.bjps.2008.06.059 10.1597/1545-1569(2003)040<0203:SCPPWA>2.0.CO;2 10.1097/01.prs.0000188856.20267.2b 10.1097/00006534-197111000-00047 10.1597/1545-1569(2001)038<0421:MRIITE>2.0.CO;2 |
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Copyright | 2016 American Society of Plastic Surgeons Copyright © 2016 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. All rights reserved. 2016 |
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Snippet | BACKGROUND:Although cleft lip and cleft palate are among the most common congenital malformations, the presence of an isolated congenital palatal fistula along... Although cleft lip and cleft palate are among the most common congenital malformations, the presence of an isolated congenital palatal fistula along with a... UNLABELLEDAlthough cleft lip and cleft palate are among the most common congenital malformations, the presence of an isolated congenital palatal fistula along... |
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Title | Congenital Palatal Fistula Associated with Submucous Cleft Palate |
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