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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Symptomatic measures aimed at relieving the distressing local and systemic complaints have been described as the main line of management of KFD. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.
Subscribe to our Newsletter. Histopathology Lymphatic organ diseases Lymphoid-related cutaneous conditions Rare diseases. Kikuchi disease is a self-limiting illness which has symptoms which may overlap with Hodgkin’s lymphoma leading to misdiagnosis in some patients. Kikuchi-Fujimoto necrotizing lymphadenitis associated with brucellosis [Article in Spanish].
Os exames laboratoriais mostraram: J Otolaryngol Head Neck Surg. Orphanet J Rare Dis.
Enfermedad de Kikuchi-Fujimoto en región inguinal | Anales de Pediatría (English Edition)
CiteScore measures average citations received per document published. Human leukocyte antigen class II genes are more frequent in patients with Kikuchi disease, suggesting a genetic predisposition to the proposed autoimmune response. The Impact Factor measures xe average number of citations received in a particular year by papers published in the journal during the two receding years. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.
An Med Int, 16pp. Print Send to a friend Export reference Mendeley Statistics. Enfermedad de Kikuchi-Fujimoto linfadenitis enfemredad histiocitaria. An Esp Pediatr, 42pp.
Kikuchi disease Synonyms Histiocytic necrotizing lymphadenitis Micrograph of a lymph node with Kikuchi disease showing the characteristic features abundant histiocytesnecrosis without neutrophils. Kikuch systemic disorders associated with interstitial lung disease. The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: From Wikipedia, the free encyclopedia. Acta Haematol, 35pp. Entretanto, a idade dos pacientes pode variar de 6 a 80 anos.
Continuing navigation will be considered as acceptance of this use. Si continua navegando, consideramos que acepta su uso. This page was last edited on 22 Julyat Necrotizing cervical lymphadenopathy caused by Kikuchi-Fujimoto disease. Alguns autores descreveram 25 casos de DKF.
Descrevemos dois casos de DKF. Continuing navigation will be considered as acceptance of this use. Curr Opin Pulm Med. This item has received.
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Cir Pediatr, 13pp. The differential diagnosis of Kikuchi disease includes systemic lupus erythematosus SLEdisseminated tuberculosislymphomasarcoidosisand viral lymphadenitis. Exames laboratoriais mostraram FAN 1: D ICD – Enfermfdad new clinicopathological entity. 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.