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Histiocitosis de Células de Langerhans en el área maxilofacial en adultos. Informe de tres casos / Langerhans cell histiocytosis in the maxillofacial area in adults. Report of three cases
García de Marcos, José Antonio; Dean Ferrer, Alicia; Alamillos Granados, Francisco; Ruiz Masera, Juan José; Barrios Sánchez, Gracia; Romero Ortiz, Ana Isabel; Calderón Bohórquez, José María; Valenzuela Salas, Borja.
Affiliation
  • García de Marcos, José Antonio; Albacete University Hospital. Albacete. Spain
  • Dean Ferrer, Alicia; University Hospital “Reina Sofía”. Cordoba. Spain
  • Alamillos Granados, Francisco; University Hospital “Reina Sofía”. Cordoba. Spain
  • Ruiz Masera, Juan José; Córdoba University. Córdoba. Spain
  • Barrios Sánchez, Gracia; Córdoba University. Córdoba. Spain
  • Romero Ortiz, Ana Isabel; University Hospital “Reina Sofía”. Cordoba. Spain
  • Calderón Bohórquez, José María; University Hospital “Reina Sofía”. Cordoba. Spain
  • Valenzuela Salas, Borja; University Hospital “Reina Sofía”. Cordoba. Spain
Med. oral patol. oral cir. bucal (Internet) ; 12(2): E145-E150, mar. 2007. ilus, tab
Article in Es | IBECS | ID: ibc-053391
Responsible library: ES1.1
Localization: ES1.1 - BNCS
RESUMEN
La Histiocitosis de Células de Langerhans (HCL), es una enfermedad de etiología desconocida, que se caracteriza por la proliferación e infiltración anormal, de órganos, por células de Langerhans patológicas. Afecta predominantementea pacientes en edad pediátrica, siendo en adultos la incidencia de la enfermedad de uno a dos casos por millón de habitantes. Las manifestaciones en cabeza y cuello aparecen en casi un 90% de los casos. El diagnóstico se obtiene por medios anatomopatológicos, siendo necesarias una serie de pruebas, determinantes de extensión, en todos los pacientes diagnosticados de HCL. No existen estudios, controlados, que determinen un tratamiento óptimo para la HCL. El pronósticode esta enfermedad en adultos es generalmente bueno debido a la lenta evolución de la enfermedad y a su buena respuesta al tratamiento. Presentamos una revisión de tres casos de HCL, de 16, 24 y 28 años de edad, con manifestación primaria en el área Maxilofacial. Así mismo, realizamos una revisión de la literatura
ABSTRACT
Langerhans cell histiocytosis (LCH) is a disease of unknown etiology, characterized by proliferation of pathological Langerhans cells within different organs. It mainly affects children, but adult cases also occur, with an incidence rate of one to two per million. The head and neck are affected in almost 90% of cases. Diagnosis is made by means of histopathologicalanalysis, and imaging studies are necessary in order to determine extent of the disease. There are no controlled trials proposing an optimal treatment protocol for LCH. Prognosis in adults is generally good due to the slow evolution of the disease and its favourable response to treatment. In our report, we present three cases of LCH in patients aged 16, 24, and 28 years respectively, with primary manifestation in the maxillofacial area. A literature review was also conducted
Subject(s)
Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Orbital Neoplasms / Maxillary Neoplasms / Histiocytosis, Langerhans-Cell Type of study: Diagnostic study / Practice guideline / Prognostic study Limits: Adolescent / Adult / Female / Humans / Male Language: Spanish Journal: Med. oral patol. oral cir. bucal (Internet) Year: 2007 Document type: Article Institution/Affiliation country: Albacete University Hospital/Spain / Córdoba University/Spain / University Hospital “Reina Sofía”/Spain
Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Orbital Neoplasms / Maxillary Neoplasms / Histiocytosis, Langerhans-Cell Type of study: Diagnostic study / Practice guideline / Prognostic study Limits: Adolescent / Adult / Female / Humans / Male Language: Spanish Journal: Med. oral patol. oral cir. bucal (Internet) Year: 2007 Document type: Article Institution/Affiliation country: Albacete University Hospital/Spain / Córdoba University/Spain / University Hospital “Reina Sofía”/Spain
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