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
Main Authors: Eshete, Mekonen, Camison, Liliana, Abate, Fikre, Hailu, Taye, Demissie, Yohannes, Mohammed, Ibrahim, Butali, Azeez, Losken, H Wolfgang, Spiess, Alexander M
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Published: United States American Society of Plastic Surgeons 01-02-2016
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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.
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
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  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
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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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References 13126438 - Br J Plast Surg. 1954 Jan;6(4):264-82
11522163 - Cleft Palate Craniofac J. 2001 Sep;38(5):421-31
19816307 - J Craniofac Surg. 2009 Sep;20(5):1606-7
12605529 - Cleft Palate Craniofac J. 2003 Mar;40(2):203-6
16267473 - Plast Reconstr Surg. 2005 Nov;116(6):1821-2
10036656 - J Craniomaxillofac Surg. 1998 Dec;26(6):391-3
16681410 - Cleft Palate Craniofac J. 2006 May;43(3):363-6
5091374 - Plast Reconstr Surg. 1971 Jul;48(1):44-7
5929054 - Plast Reconstr Surg. 1966 Dec;38(6):552-4
25298946 - Int J Appl Basic Med Res. 2014 Sep;4(Suppl 1):S56-7
5074937 - Plast Reconstr Surg. 1972 Oct;50(4):390-4
18945656 - J Plast Reconstr Aesthet Surg. 2009 Nov;62(11):e509-10
Mehendale (R5-17-20160305) 2003; 40
Smiley (R10-17-20160305) 1972; 50
Kuehn (R12-17-20160305) 2001; 38
Calnan (R9-17-20160305) 1954; 6
Tosun (R11-17-20160305) 2005; 116
Rogers (R1-17-20160305) 2006; 43
Abdel-Aziz (R15-17-20160305) 2009; 62
Cheng (R3-17-20160305) 1998; 26
Karacan (R8-17-20160305) 2009; 20
Shah (R14-17-20160305) 2014; 4
Fara (R4-17-20160305) 1971; 48
Trelat (R6-17-20160305) 1870; 96
Lynch (R7-17-20160305) 1966; 38
References_xml – volume: 26
  start-page: 391
  year: 1998
  ident: R3-17-20160305
  publication-title: J Craniomaxillofac Surg
  doi: 10.1016/S1010-5182(98)80073-5
  contributor:
    fullname: Cheng
– volume: 38
  start-page: 552
  year: 1966
  ident: R7-17-20160305
  publication-title: Plast Reconstr Surg
  doi: 10.1097/00006534-196638060-00010
  contributor:
    fullname: Lynch
– volume: 96
  start-page: 553
  year: 1870
  ident: R6-17-20160305
  publication-title: Lancet
  contributor:
    fullname: Trelat
– volume: 6
  start-page: 264
  year: 1954
  ident: R9-17-20160305
  publication-title: Br J Plast Surg
  doi: 10.1016/S0007-1226(53)80060-3
  contributor:
    fullname: Calnan
– volume: 43
  start-page: 363
  year: 2006
  ident: R1-17-20160305
  publication-title: Cleft Palate Craniofac J
  doi: 10.1597/05-0131.1
  contributor:
    fullname: Rogers
– volume: 50
  start-page: 390
  year: 1972
  ident: R10-17-20160305
  publication-title: Plast Reconstr Surg
  doi: 10.1097/00006534-197210000-00015
  contributor:
    fullname: Smiley
– volume: 20
  start-page: 1606
  year: 2009
  ident: R8-17-20160305
  publication-title: J Craniofac Surg
  doi: 10.1097/SCS.0b013e3181b14722
  contributor:
    fullname: Karacan
– volume: 4
  start-page: S56
  year: 2014
  ident: R14-17-20160305
  publication-title: Int J Appl Basic Med Res
  doi: 10.4103/2229-516X.140745
  contributor:
    fullname: Shah
– volume: 62
  start-page: e509
  year: 2009
  ident: R15-17-20160305
  publication-title: J Plast Reconstr Aesthet Surg
  doi: 10.1016/j.bjps.2008.06.059
  contributor:
    fullname: Abdel-Aziz
– volume: 40
  start-page: 203
  year: 2003
  ident: R5-17-20160305
  publication-title: Cleft Palate Craniofac J
  doi: 10.1597/1545-1569(2003)040<0203:SCPPWA>2.0.CO;2
  contributor:
    fullname: Mehendale
– volume: 116
  start-page: 1821
  year: 2005
  ident: R11-17-20160305
  publication-title: Plast Reconstr Surg
  doi: 10.1097/01.prs.0000188856.20267.2b
  contributor:
    fullname: Tosun
– volume: 48
  start-page: 44
  year: 1971
  ident: R4-17-20160305
  publication-title: Plast Reconstr Surg
  doi: 10.1097/00006534-197111000-00047
  contributor:
    fullname: Fara
– volume: 38
  start-page: 421
  year: 2001
  ident: R12-17-20160305
  publication-title: Cleft Palate Craniofac J
  doi: 10.1597/1545-1569(2001)038<0421:MRIITE>2.0.CO;2
  contributor:
    fullname: Kuehn
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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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