Treatment of papillomatous lesions in a patient with Goltz syndrome—A case report
Background Goltz syndrome, also known as focal dermal hypoplasia (FDH), is a rare genetic disorder that affects ectodermal and mesodermal tissues. The purpose of this study is to report the treatment of papillomatous lesions in the orofacial region of a patient with Goltz syndrome. Case description...
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Published in: | Oral surgery Vol. 15; no. 4; pp. 618 - 623 |
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Abstract | Background
Goltz syndrome, also known as focal dermal hypoplasia (FDH), is a rare genetic disorder that affects ectodermal and mesodermal tissues. The purpose of this study is to report the treatment of papillomatous lesions in the orofacial region of a patient with Goltz syndrome.
Case description
A 31‐year‐old male patient was attended at Dental School of Federal University of Goiás with the chief complaint of discomfort during speaking and eating, due to the presence of a papillomatous lesion at the labial commissure. During the physical examination, syndrome characteristics were found, such as unilateral anophthalmia; atrophic cutaneous lesions of different intensities of pigmentation, mostly on the arms and neck; sparse hair; ectrodactyly, being the right hand was shaped like a ‘lobster claw’; and body asymmetry. In addition, papillomatous lesions at the right labial commissure and on the dorsum of the tongue were noted, which were subsequently removed with surgical laser. The microscopic diagnosis of the lesions was a squamous papilloma.
Conclusion
The proposed surgical treatment was well succeeded, and the rarity of the present case also having Goltz syndrome is an uncommon condition in males. |
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AbstractList | Background
Goltz syndrome, also known as focal dermal hypoplasia (FDH), is a rare genetic disorder that affects ectodermal and mesodermal tissues. The purpose of this study is to report the treatment of papillomatous lesions in the orofacial region of a patient with Goltz syndrome.
Case description
A 31‐year‐old male patient was attended at Dental School of Federal University of Goiás with the chief complaint of discomfort during speaking and eating, due to the presence of a papillomatous lesion at the labial commissure. During the physical examination, syndrome characteristics were found, such as unilateral anophthalmia; atrophic cutaneous lesions of different intensities of pigmentation, mostly on the arms and neck; sparse hair; ectrodactyly, being the right hand was shaped like a ‘lobster claw’; and body asymmetry. In addition, papillomatous lesions at the right labial commissure and on the dorsum of the tongue were noted, which were subsequently removed with surgical laser. The microscopic diagnosis of the lesions was a squamous papilloma.
Conclusion
The proposed surgical treatment was well succeeded, and the rarity of the present case also having Goltz syndrome is an uncommon condition in males. BackgroundGoltz syndrome, also known as focal dermal hypoplasia (FDH), is a rare genetic disorder that affects ectodermal and mesodermal tissues. The purpose of this study is to report the treatment of papillomatous lesions in the orofacial region of a patient with Goltz syndrome.Case descriptionA 31‐year‐old male patient was attended at Dental School of Federal University of Goiás with the chief complaint of discomfort during speaking and eating, due to the presence of a papillomatous lesion at the labial commissure. During the physical examination, syndrome characteristics were found, such as unilateral anophthalmia; atrophic cutaneous lesions of different intensities of pigmentation, mostly on the arms and neck; sparse hair; ectrodactyly, being the right hand was shaped like a ‘lobster claw’; and body asymmetry. In addition, papillomatous lesions at the right labial commissure and on the dorsum of the tongue were noted, which were subsequently removed with surgical laser. The microscopic diagnosis of the lesions was a squamous papilloma.ConclusionThe proposed surgical treatment was well succeeded, and the rarity of the present case also having Goltz syndrome is an uncommon condition in males. |
Author | Siqueira, Giovanna Mourão Cavalcante, Marina Bertolucci Coimbra Fonseca, Mônatha Távora Goulart, Douglas Rangel Arantes, Diego Antônio Costa Silva, Amanda Meira Fernandez Costa, Nádia do Lago |
Author_xml | – sequence: 1 givenname: Amanda Meira Fernandez surname: Silva fullname: Silva, Amanda Meira Fernandez organization: Federal University of Goiás (FO‐UFG) – sequence: 2 givenname: Giovanna Mourão surname: Siqueira fullname: Siqueira, Giovanna Mourão organization: Federal University of Goiás (FO‐UFG) – sequence: 3 givenname: Marina Bertolucci Coimbra surname: Cavalcante fullname: Cavalcante, Marina Bertolucci Coimbra organization: Federal University of Goiás (FO‐UFG) – sequence: 4 givenname: Mônatha Távora surname: Fonseca fullname: Fonseca, Mônatha Távora organization: Federal University of Goiás (FO‐UFG) – sequence: 5 givenname: Diego Antônio Costa surname: Arantes fullname: Arantes, Diego Antônio Costa organization: Federal University of Goiás (FO‐UFG) – sequence: 6 givenname: Nádia do Lago surname: Costa fullname: Costa, Nádia do Lago organization: Federal University of Goiás (FO‐UFG) – sequence: 7 givenname: Douglas Rangel orcidid: 0000-0001-8339-3660 surname: Goulart fullname: Goulart, Douglas Rangel email: douglasgoulart@ufg.br organization: Federal University of Goiás (FO‐UFG) |
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Cites_doi | 10.1007/s10103-013-1401-7 10.1002/ajmg.c.31472 10.1053/j.semdp.2014.12.003 10.4103/ijd.IJD_317_17 10.1001/archderm.1992.01680180102015 10.1001/archderm.1962.01590120006002 10.1002/ajmg.c.31470 10.1111/j.1440-0960.2010.00662.x 10.4248/IJOS10065 10.1002/ajmg.c.31480 10.1002/ajmg.c.31475 10.1002/ccr3.1783 |
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References | 2017; 62 2018; 6 2016; 172C 1990 2019; 24 2015; 30 2015; 32 2011; 52 1992; 128 1962; 86 2010; 2 1999; 9 2007; 38 Gordjani N (e_1_2_6_10_1) 1999; 9 Boj JR (e_1_2_6_14_1) 2007; 38 Ghosh SK (e_1_2_6_4_1) 2017; 62 Gorlin RJ (e_1_2_6_8_1) 1990 Toledano‐Serrabona J (e_1_2_6_13_1) 2019; 24 e_1_2_6_9_1 e_1_2_6_5_1 e_1_2_6_7_1 e_1_2_6_6_1 e_1_2_6_3_1 e_1_2_6_11_1 e_1_2_6_2_1 e_1_2_6_12_1 e_1_2_6_17_1 e_1_2_6_18_1 e_1_2_6_15_1 e_1_2_6_16_1 |
References_xml | – volume: 86 start-page: 708 issue: 6 year: 1962 end-page: 17 article-title: Focal dermal hypoplasia publication-title: Arch Dermatol – volume: 38 start-page: 307 year: 2007 end-page: 12 article-title: Laser treatment of an oral papilloma in the pediatric dental office: a case report publication-title: Quintessence Int – volume: 6 start-page: 2103 year: 2018 end-page: 10 article-title: Goltz syndrome in males: A clinical report of a male patient carrying a novel PORCN variant and a review of the literature publication-title: Clin Case Rep – volume: 24 start-page: e433 year: 2019 end-page: 7 article-title: Recurrence rate of oral squamous cell papilloma after excision with surgical scalpel or laser therapy: a retrospective cohort study publication-title: Med Oral Patol Oral Cir Bucal – volume: 172C start-page: 44 year: 2016 end-page: 51 article-title: Dermatologic findings of focal dermal hypoplasia (Goltz syndrome) publication-title: Am J Med Genet C Semin Med Genet – volume: 32 start-page: 3 year: 2015 end-page: 11 article-title: Human papillomavirus and Epstein‐Barr virus associated conditions of the oral mucosa publication-title: Semin Diagn Pathol – volume: 9 start-page: 618 year: 1999 end-page: 20 article-title: Focal dermal hypoplasia (Goltz‐Gorlin syndrome) associated with obstructive papillomatosis of the larynx and hypopharynx publication-title: Eur J Dermatol – volume: 30 start-page: 747 year: 2015 end-page: 51 article-title: Human papilloma virus lesions of the oral cavity: healing and relapse after treatment with 810–980 nm diode laser publication-title: Lasers Med Sci – year: 1990 – volume: 128 start-page: 1108 year: 1992 end-page: 11 article-title: Focal dermal hypoplasia syndrome: an update publication-title: Arch Dermatol – volume: 172C start-page: 41 year: 2016 end-page: 3 article-title: The orthopedic characterization of Goltz syndrome publication-title: Am J Med Genet C Semin Med Genet – volume: 62 start-page: 498 year: 2017 end-page: 504 article-title: Focal dermal hypoplasia (Goltz syndrome): a cross‐sectional study from Eastern India publication-title: Indian J Dermatol – volume: 52 start-page: 48 year: 2011 end-page: 51 article-title: A case of mosaic Goltz syndrome (focal dermal hypoplasia) in a male patient publication-title: Australas J Dermatol – volume: 172C start-page: 44 year: 2016 end-page: 51 article-title: Dermatologic findings of focal dermal hypoplasia (Goltz syndrome) publication-title: Am J Med Genet Part C Semin Med Genet – volume: 2 start-page: 222 year: 2010 end-page: 5 article-title: Squamous papilloma: case report and review of literature publication-title: Int J Oral Sci – volume: 172C start-page: 59 year: 2016 end-page: 63 article-title: Ophthalmologic manifestations of focal dermal hypoplasia (Goltz syndrome): a case series of 18 patients publication-title: Am J Med Genet C Semin Med Genet – volume: 172C start-page: 3 year: 2016 end-page: 6 article-title: International research symposium on Goltz syndrome publication-title: Am J Med Genet C Semin Med Genet – ident: e_1_2_6_15_1 doi: 10.1007/s10103-013-1401-7 – volume-title: Syndromes of the head and neck year: 1990 ident: e_1_2_6_8_1 contributor: fullname: Gorlin RJ – ident: e_1_2_6_9_1 doi: 10.1002/ajmg.c.31472 – ident: e_1_2_6_11_1 doi: 10.1053/j.semdp.2014.12.003 – volume: 62 start-page: 498 year: 2017 ident: e_1_2_6_4_1 article-title: Focal dermal hypoplasia (Goltz syndrome): a cross‐sectional study from Eastern India publication-title: Indian J Dermatol doi: 10.4103/ijd.IJD_317_17 contributor: fullname: Ghosh SK – ident: e_1_2_6_6_1 doi: 10.1001/archderm.1992.01680180102015 – volume: 24 start-page: e433 year: 2019 ident: e_1_2_6_13_1 article-title: Recurrence rate of oral squamous cell papilloma after excision with surgical scalpel or laser therapy: a retrospective cohort study publication-title: Med Oral Patol Oral Cir Bucal contributor: fullname: Toledano‐Serrabona J – ident: e_1_2_6_16_1 doi: 10.1002/ajmg.c.31472 – ident: e_1_2_6_2_1 doi: 10.1001/archderm.1962.01590120006002 – ident: e_1_2_6_17_1 doi: 10.1002/ajmg.c.31470 – ident: e_1_2_6_5_1 doi: 10.1111/j.1440-0960.2010.00662.x – ident: e_1_2_6_12_1 doi: 10.4248/IJOS10065 – ident: e_1_2_6_18_1 doi: 10.1002/ajmg.c.31480 – ident: e_1_2_6_7_1 doi: 10.1002/ajmg.c.31475 – volume: 9 start-page: 618 year: 1999 ident: e_1_2_6_10_1 article-title: Focal dermal hypoplasia (Goltz‐Gorlin syndrome) associated with obstructive papillomatosis of the larynx and hypopharynx publication-title: Eur J Dermatol contributor: fullname: Gordjani N – ident: e_1_2_6_3_1 doi: 10.1002/ccr3.1783 – volume: 38 start-page: 307 year: 2007 ident: e_1_2_6_14_1 article-title: Laser treatment of an oral papilloma in the pediatric dental office: a case report publication-title: Quintessence Int contributor: fullname: Boj JR |
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Snippet | Background
Goltz syndrome, also known as focal dermal hypoplasia (FDH), is a rare genetic disorder that affects ectodermal and mesodermal tissues. The purpose... BackgroundGoltz syndrome, also known as focal dermal hypoplasia (FDH), is a rare genetic disorder that affects ectodermal and mesodermal tissues. The purpose... |
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SubjectTerms | Anophthalmia Case reports ectodermal dysplasia Ectrodactyly Focal dermal hypoplasia Genetic disorders HPV Hypoplasia lasers Lesions Papilloma Patients Pigmentation Tumors |
Title | Treatment of papillomatous lesions in a patient with Goltz syndrome—A case report |
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