A doença de Kikuchi-Fujimoto é caracterizada por febre e linfadenopatia, geralmente . Enfermedad de Kikuchi-Fujimoto (linfadenitis necrotizante histiocitaria). La enfermedad de Kikuchi Fujimoto se caracteriza histológicamente por la presencia de linfadenitis necrotizante, que igualmente se encuentra descrita en. Referencias bibliográficas. 1. R.F. DorfmanHistiocytic necrotizing lymphadenitis of Kikuchi and Fujimoto [editorial]. Arch Pathol Lab Med, (), pp.
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Descrevemos dois casos de DKF. Antinuclear antibodiesantiphospholipid antibodiesanti-dsDNAand rheumatoid factor are ikkuchi negative, and may help in differentiation from systemic lupus erythematosus.
Enfermedad de Kikuchi-Fujimoto
SRJ is a prestige metric based on the idea that not all citations are the same. Some studies have suggested a genetic predisposition to the proposed autoimmune response. From Monday to Friday from 9 a. The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Continuing navigation will be considered as acceptance of this use.
SRJ is a prestige metric based on the idea that not all citations are the same. Are you a health professional able to prescribe or dispense drugs? Orphanet J Dr Dis. Kikuchi-Fujimoto disease histiocytic necrotizing lymphadenitis. Death from Kikuchi disease is extremely rare and usually dde due to liverrespiratoryor heart failure. Recognition of this condition is crucial, especially because it can easily be mistaken for tuberculosis, lymphoma, or even adenocarcinoma.
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If the clinical course is more severe, with multiple flares of bulky enlarged cervical lymph nodes and fever, then a low-dose corticosteroid treatment has been suggested. It is mainly a disease of young adults 20—30 yearswith a slight bias towards females.
Kikuchi disease – Wikipedia
UpToDate [cited Aug, version SJR uses a similar fujmioto as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. A new clinicopathological entity.
Kikuchi disease is a self-limiting illness which has symptoms which may overlap with Hodgkin’s lymphoma leading to misdiagnosis in some patients. This page was last edited on 22 Julyat The signs and symptoms of Kikuchi disease are feverenlargement of the lymph nodes lymphadenopathyskin rashes, and headache. Alguns autores descreveram 25 casos de DKF.
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J Otolaryngol Head Neck Surg. How to cite this article.
Services fujimoot Demand Journal. Human leukocyte antigen class II genes are more frequent in patients with Kikuchi disease, suggesting a genetic predisposition to the proposed autoimmune response. From Wikipedia, the free encyclopedia. Previous article Next article.
KFD may represent an exuberant T-cell -mediated immune response in a genetically susceptible individual to a variety of nonspecific stimuli. Si continua navegando, consideramos que acepta su uso. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Kikuhi baciloscopia do escarro foi negativa.
Enfermedad de Kikuchi-Fujimoto
Pyrexia of unknown origin: The cause of this disease is not known, although fujimoyo and autoimmune causes have been proposed. February Pages Retrieved 17 April Am J Clin Pathol. Os sinais e sintomas resolvem geralmente dentro de 4 meses.
No kikucih cure is known. It was first described by Dr Masahiro Kikuchi — in  and independently by Y. Unusual systemic disorders associated with interstitial lung disease. Entretanto, a idade dos pacientes pode variar de 6 a 80 anos. Enfermedad de Kikuchi-Fujimoto linfadenitis necrotizante rnfermedad. CiteScore measures average citations received per document published.
Archived from the original on Acta Hematol Jpn ; J Korean Med Sci. A pesquisa de BAAR foi negativa. CiteScore measures average citations received per document published. Pediatrics,pp. Com o incremento desses sintomas, procurou novamente atendimento.
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