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Histiocitosis X: revisión de la literatura y presentación de caso clínico / Histiocytosis X: a review of the literature and clinical case presentation
Valcanaia, Túlio Del Conte; Portal Bustamante, Neme; Chaves Júnior, Airton Charles; Oliveira, Henrique Telles Ramos de; Oliveira, Marília Gerhardt de.
Affiliation
  • Valcanaia, Túlio Del Conte; Universidade do Vale do Itajaí. BR
  • Portal Bustamante, Neme; Universidad Nacional Federico Villareal. Lima. PE
  • Chaves Júnior, Airton Charles; Pontificia Universidad Católica do Rio Grande do Sul. BR
  • Oliveira, Henrique Telles Ramos de; Pontificia Universidad Católica do Rio Grande do Sul. BR
  • Oliveira, Marília Gerhardt de; Pontificia Universidad Católica do Rio Grande do Sul. BR
Meet. odontol ; 4(14): 95-102, 2007. ilus
Article in Spanish | LIPECS | ID: biblio-1109427
Responsible library: PE1.1
Localization: PE1.1
RESUMEN
La Histiocitosis X es una enfermedad rara sin causa conocida, que está caracterizada por la presencia de células histiocitáricas que deben ser tratadas para prevenir su evolución. Este artículo llega a través de una revisión de la literatura y presentación de caso clínico de un paciente del sexo femenino, que fue presentado con lesiones en la región posterior de la mandíbula, al ser tomado las radiografías se evidenció áreas alveolares de radiolucidez compatible con exodoncias recientes. El diagnóstico inicial clínico era tendencioso para la osteomielitis, sin embargo después del examen histopatológico, fue evidente que estaba con lesión rara. Su tratamiento basado en la literatura se describe más adelante con éxito.
ABSTRACT
Histiocytosis X is a rare disease with an unknown cause which characterizes by the presence of histiocytic cells which must be treated to prevent their development. This article is developed through a literature review and a clinical case presentation of a female patient who had lesions in the posterior region of her jaw and by taking X-rays; compatible radiolucency alveolar areas with recent exodontics could have been noticed. Initial clinical diagnosis was tendentious for osteomyelitis; nevertheless, after histopathological examination, it was observed that she had this rare lesion. The treatment based on the literature is described next with success.
Subject(s)
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Collection: National databases / Peru Database: LIPECS Main subject: Eosinophilic Granuloma / Histiocytosis, Langerhans-Cell Limits: Adult / Female / Humans Language: Spanish Journal: Meet. odontol Year: 2007 Document type: Article Institution/Affiliation country: Pontificia Universidad Católica do Rio Grande do Sul/BR / Universidad Nacional Federico Villareal/PE / Universidade do Vale do Itajaí/BR
Search on Google
Collection: National databases / Peru Database: LIPECS Main subject: Eosinophilic Granuloma / Histiocytosis, Langerhans-Cell Limits: Adult / Female / Humans Language: Spanish Journal: Meet. odontol Year: 2007 Document type: Article Institution/Affiliation country: Pontificia Universidad Católica do Rio Grande do Sul/BR / Universidad Nacional Federico Villareal/PE / Universidade do Vale do Itajaí/BR
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