Síndrome KID en gemelos monocigotos asociado con carcinoma de células escamosas.
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| Title: | Síndrome KID en gemelos monocigotos asociado con carcinoma de células escamosas. |
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| Alternate Title: | KID syndrome in monozygotic twins associated with squamous cell carcinoma. |
| Authors: | Mendoza Ochoa, Andrea Melissa1, Hernández Peralta, Sarah Lizette2 saralizhp@hotmail.com, Moreno Alanís, Jessica Aylin1, García Vargas, Alejandro3, Salazar Torres, Francisco Javier2, Manzotti Rodríguez, Carolina4, Romo Sánchez, Conrado2, Varela Coronado, Lauro Francisco2 |
| Source: | Dermatología Revista Mexicana. 2024 Supplement, Vol. 68, pS99-S103. 5p. |
| Abstract (English): | BACKGROUND: Keratitis-ichthyosis-deafness (KID) syndrome is a keratinization disorder characterized by ichthyosiform dermatosis, keratitis and deafness, with a predisposition to the development of skin infections and neoplasms. CLINICAL CASES: This paper reports the case of two male twins, 39-years-old, who had alopecia, ichthyosis, sensorineural deafness and keratitis from birth. In addition, one of them presented a dermatosis in the left frontotemporal region, of one month of evolution, consisting of three exophytic neoformations of up to 5 cm in diameter, which histopathologically corresponded to squamous cell carcinomas. CONCLUSIONS: KID syndrome is associated with the development of multiple squamous cell carcinoma, so, the timely diagnosis and lifelong multidisciplinary follow-up are essential to improve the survival and quality of life of these patients. [ABSTRACT FROM AUTHOR] |
| Abstract (Spanish): | ANTECEDENTES: El síndrome de queratitis, ictiosis y sordera (KID) es un trastorno de la queratinización caracterizado por dermatosis ictiosiforme, queratitis y sordera, con predisposición a infecciones cutáneas y neoplasias. CASOS CLÍNICOS: Se comunica el caso de dos gemelos masculinos, de 39 años, quienes padecían alopecia, ictiosis, sordera neurosensorial y queratitis desde el nacimiento. Además, uno de ellos tenía una dermatosis en la región frontotemporal izquierda, de un mes de evolución, constituida por tres neoformaciones exofíticas de hasta 5 cm de diámetro, que histopatológicamente correspondieron a carcinomas de células escamosas. CONCLUSIONES: El síndrome KID se asocia con el carcinoma espinocelular múltiple, por ello es fundamental el diagnóstico oportuno y el seguimiento multidisciplinario de por vida para mejorar la supervivencia y la calidad de vida de los pacientes. [ABSTRACT FROM AUTHOR] |
| Copyright of Dermatología Revista Mexicana is the property of Edicion y Farmacia S.A. de C.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | MedicLatina |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: lth DbLabel: MedicLatina An: 184802945 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Síndrome KID en gemelos monocigotos asociado con carcinoma de células escamosas. – Name: TitleAlt Label: Alternate Title Group: TiAlt Data: KID syndrome in monozygotic twins associated with squamous cell carcinoma. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Mendoza+Ochoa%2C+Andrea+Melissa%22">Mendoza Ochoa, Andrea Melissa</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Hernández+Peralta%2C+Sarah+Lizette%22">Hernández Peralta, Sarah Lizette</searchLink><relatesTo>2</relatesTo><i> saralizhp@hotmail.com</i><br /><searchLink fieldCode="AR" term="%22Moreno+Alanís%2C+Jessica+Aylin%22">Moreno Alanís, Jessica Aylin</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22García+Vargas%2C+Alejandro%22">García Vargas, Alejandro</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Salazar+Torres%2C+Francisco+Javier%22">Salazar Torres, Francisco Javier</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Manzotti+Rodríguez%2C+Carolina%22">Manzotti Rodríguez, Carolina</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Romo+Sánchez%2C+Conrado%22">Romo Sánchez, Conrado</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Varela+Coronado%2C+Lauro+Francisco%22">Varela Coronado, Lauro Francisco</searchLink><relatesTo>2</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Dermatología+Revista+Mexicana%22">Dermatología Revista Mexicana</searchLink>. 2024 Supplement, Vol. 68, pS99-S103. 5p. – Name: Abstract Label: Abstract (English) Group: Ab Data: BACKGROUND: Keratitis-ichthyosis-deafness (KID) syndrome is a keratinization disorder characterized by ichthyosiform dermatosis, keratitis and deafness, with a predisposition to the development of skin infections and neoplasms. CLINICAL CASES: This paper reports the case of two male twins, 39-years-old, who had alopecia, ichthyosis, sensorineural deafness and keratitis from birth. In addition, one of them presented a dermatosis in the left frontotemporal region, of one month of evolution, consisting of three exophytic neoformations of up to 5 cm in diameter, which histopathologically corresponded to squamous cell carcinomas. CONCLUSIONS: KID syndrome is associated with the development of multiple squamous cell carcinoma, so, the timely diagnosis and lifelong multidisciplinary follow-up are essential to improve the survival and quality of life of these patients. [ABSTRACT FROM AUTHOR] – Name: Abstract Label: Abstract (Spanish) Group: Ab Data: ANTECEDENTES: El síndrome de queratitis, ictiosis y sordera (KID) es un trastorno de la queratinización caracterizado por dermatosis ictiosiforme, queratitis y sordera, con predisposición a infecciones cutáneas y neoplasias. CASOS CLÍNICOS: Se comunica el caso de dos gemelos masculinos, de 39 años, quienes padecían alopecia, ictiosis, sordera neurosensorial y queratitis desde el nacimiento. Además, uno de ellos tenía una dermatosis en la región frontotemporal izquierda, de un mes de evolución, constituida por tres neoformaciones exofíticas de hasta 5 cm de diámetro, que histopatológicamente correspondieron a carcinomas de células escamosas. CONCLUSIONES: El síndrome KID se asocia con el carcinoma espinocelular múltiple, por ello es fundamental el diagnóstico oportuno y el seguimiento multidisciplinario de por vida para mejorar la supervivencia y la calidad de vida de los pacientes. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Dermatología Revista Mexicana is the property of Edicion y Farmacia S.A. de C.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=lth&AN=184802945 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.24245/drm/bmu.v68iS1.10138 Languages: – Code: spa Text: Spanish PhysicalDescription: Pagination: PageCount: 5 StartPage: S99 Titles: – TitleFull: Síndrome KID en gemelos monocigotos asociado con carcinoma de células escamosas. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Mendoza Ochoa, Andrea Melissa – PersonEntity: Name: NameFull: Hernández Peralta, Sarah Lizette – PersonEntity: Name: NameFull: Moreno Alanís, Jessica Aylin – PersonEntity: Name: NameFull: García Vargas, Alejandro – PersonEntity: Name: NameFull: Salazar Torres, Francisco Javier – PersonEntity: Name: NameFull: Manzotti Rodríguez, Carolina – PersonEntity: Name: NameFull: Romo Sánchez, Conrado – PersonEntity: Name: NameFull: Varela Coronado, Lauro Francisco IsPartOfRelationships: – BibEntity: Dates: – D: 02 M: 11 Text: 2024 Supplement Type: published Y: 2024 Identifiers: – Type: issn-print Value: 01854038 Numbering: – Type: volume Value: 68 Titles: – TitleFull: Dermatología Revista Mexicana Type: main |
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