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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SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Acta Hematol Jpn ; Cir Pediatr, 13pp. Proc Bayl Univ Med Cent.
Awareness of this disorder helps prevent misdiagnosis and inappropriate treatment. Other autoimmune conditions and manifestations such as antiphospholipid syndromepolymyositissystemic juvenile idiopathic enfsrmedadbilateral uveitisarthritis and cutaneous necrotizing vasculitis have been linked to KFD.
Pyrexia of unknown origin: Cervical subacute necrotizing lymphadenitis.
Previous article Next article. A new clinicopathological entity. CiteScore measures average citations received per document published. Acta Haematol, 35pp.
Continuing navigation will be considered as acceptance of this use. The signs and symptoms of Kikuchi disease are feverenlargement of the lymph nodes lymphadenopathyskin rashes, and headache. 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.
Os sinais e sintomas resolvem geralmente dentro de 4 meses.
Lymph node enlargmeent usually resolves over several weeks to six months. Dr measures contextual citation impact by wighting citations based on the total number of citations in a subject field. D ICD – Histiocytic necrotizing lymphadenitis Kikuchi-Fujimoto disease: You can change the settings or obtain more information by clicking here. Aetiology of peripheral lymphadenopathy in adults: Symptomatic measures aimed at relieving the distressing local and systemic complaints have been described as the main line of management of KFD.
Orphanet J Rare Dis.
Enfermedad de Kikuchi-Fujimoto
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Infobox medical condition new. Bosch X, Guilabert A.
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US and CT apperance. A Sheep in Wolf’s Clothing”. To improve our services and products, we use “cookies” enermedad or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.
Retrieved 17 April To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. The Impact Factor measures the average number of citations received in a particular year by papers published fujimoti the journal during the two receding years.
J Comput Assist Tomogr, 23pp. This item has received. Entretanto, a idade dos pacientes pode variar de 6 a 80 anos. Nine issues are published each year, fuijmoto mostly originals, reviews and consensus documents.
It is also known as histiocytic necrotizing lymphadenitis, Kikuchi necrotizing lymphadenitis, phagocytic necrotizing lymphadenitis, subacute necrotizing lymphadenitis, and necrotizing lymphadenitis.
Si continua navegando, consideramos que acepta su uso. Kikuchi-Fujimoto disease histiocytic necrotizing lymphadenitis: Micrograph of a lymph node with Kikuchi disease showing the characteristic features abundant histiocytesnecrosis without neutrophils. Services on Demand Journal.