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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D ICD – SRJ is a prestige metric based on the idea that not all citations are the same. Kikuchi’s disease is a very rare disease mainly seen in Japan.

Exames laboratoriais mostraram FAN 1: The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: US and CT apperance. All the contents of this journal, except where otherwise noted, is licensed under enfermfdad Creative Commons Attribution License.

Services on Demand Journal. Os exames laboratoriais mostraram: SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

J Otolaryngol Head Neck Surg. Kikuchi disease is a self-limiting illness which has symptoms which may overlap with Hodgkin’s lymphoma leading to misdiagnosis in some patients.

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Kikuchi-Fujimoto disease

Kikuchi disease Synonyms Histiocytic necrotizing lymphadenitis Micrograph of a lymph node with Kikuchi disease showing the characteristic features abundant histiocytesnecrosis without neutrophils. Histiocytic necrotizing lymphadenitis Kikuchu disease: Several infectious candidates have been associated with Kikuchi disease. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.

A segunda paciente, de 58 anos, recebeu tratamento inicialmente para granulomatose de Wegener e, posteriormente, para tuberculose. Human leukocyte antigen class II genes are more frequent in patients with Kikuchi disease, suggesting a genetic predisposition to the fujmioto autoimmune response.

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Inter Med, 41pp. Continuing navigation will be considered as acceptance of this use. 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.

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. No specific cure is known.

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Pediatrics,pp. The signs and symptoms of Kikuchi disease are feverenlargement of the lymph nodes lymphadenopathyskin rashes, and headache.

Mycobacterium szulgai and Yersinia and Toxoplasma species have been implicated. The differential diagnosis of Kikuchi disease includes systemic lupus erythematosus SLEdisseminated tuberculosislymphomasarcoidosisand viral lymphadenitis. This page was last edited on 22 Julyat Death from Kikuchi disease is extremely rare and usually occurs due to liverrespiratoryor heart failure. Retrieved from ” https: Previous article Next article. Full text is only aviable in PDF.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. UpToDate [cited Aug, version Proc Bayl Univ Med Cent. It is mainly a disease of young adults 20—30 yearswith a slight bias towards females. Pyrexia of unknown origin: Views Read Edit View history. Many theories exist about the cause of KFD.