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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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Am J Clin Pathol,pp. An Med Int, 16pp. Nonsteroidal anti-inflammatory drugs NSAIDs are indicated for tender lymph nodes and fever, and corticosteroids are useful in severe extranodal or generalized disease. Aetiology of peripheral lymphadenopathy in adults: Alguns autores descreveram 25 casos de DKF. The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Orphanet J Enfwrmedad Dis.

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SRJ is a prestige metric based on the idea that not all citations are the same. Enfermedad de Kikuchi-Fujimoto linfadenitis necrotizante histiocitaria. Print Send to a friend Export reference Mendeley Statistics.


Entretanto, a idade dos pacientes pode variar de 6 a 80 anos. You can change the settings or obtain more information by clicking here. Os exames laboratoriais revelaram: KFD may represent an exuberant T-cell -mediated immune response in a genetically susceptible individual to a variety of nonspecific stimuli.

Enfermedad de Kikuchi-Fujimoto

Necrotizing cervical lymphadenopathy caused by Kikuchi-Fujimoto disease. Kikuchi disease is a self-limiting illness which has symptoms which may overlap with Hodgkin’s lymphoma leading to misdiagnosis in some patients. 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.

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Alguns autores descreveram um caso de um paciente com DKF e tuberculose pulmonar concomitantes. The cause of this disease is not known, although infectious and autoimmune causes have been proposed.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Antinuclear antibodiesantiphospholipid antibodiesanti-dsDNAand rheumatoid factor are usually negative, and may help in differentiation from systemic lupus erythematosus.


Os sinais e sintomas resolvem geralmente dentro de 4 meses.

Kikuchi-Fujimoto disease

A baciloscopia do escarro foi negativa. Are you a health professional able to prescribe or dispense drugs? It is mainly a disease of young adults 20—30 yearswith a slight bias towards females. Descrevemos dois casos de DKF. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject fujimtoo.

Other autoimmune conditions and manifestations ennfermedad as antiphospholipid syndromepolymyositissystemic juvenile idiopathic arthritisbilateral uveitisarthritis and cutaneous necrotizing vasculitis have been linked to KFD. An Esp Pediatr, 42pp. Enfermedad de Kikuchi-Fujimoto linfadenitis necrotizante histiocitaria. Abscess of thymus Thymus hyperplasia. From Wikipedia, the free encyclopedia. Unusual systemic disorders associated with interstitial lung disease.

Full text is only aviable in PDF. Are you a health professional able to prescribe or dispense drugs?