Bibliographic Details
| Title: |
Síndrome KID en gemelos monocigotos asociado con carcinoma de células escamosas. |
| 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] |
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| Database: |
MedicLatina |
