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 – Often a bout of extreme fatigue can occur – often taking hold during latter parts of the day and the affected person can be more prone to fatigue from exercise.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Treatment is largely supportive. Are you a health professional able to prescribe or dispense drugs? Exames laboratoriais mostraram FAN 1: Curr Opin Pulm Med. You can change the settings or obtain more information by clicking here. Com o incremento desses sintomas, procurou novamente atendimento.

Some studies have suggested a genetic predisposition to the proposed autoimmune response. Archived from the original on 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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UpToDate [cited Aug, version Kikuchi-Fujimoto disease histiocytic necrotizing lymphadenitis: Subscribe to our Newsletter. Enfermedad de Kikuchi-Fujimoto linfadenitis necrotizante histiocitaria. Antinuclear antibodiesantiphospholipid antibodiesanti-dsDNAand rheumatoid factor are usually negative, and may help in differentiation from systemic lupus erythematosus.

Kikuchi disease or Kikuchi-Fujimoto disease was described in ,ikuchi Japan. The cause of this disease is not known, although infectious and autoimmune causes have been proposed. Previous article Next article. Cervical lymphadenopathy due to Kikuchi disease: Nine issues are published each year, including mostly originals, reviews and consensus documents.

Kikuchi disease

Enfermedad de Kikuchi o linfadenitis necrotizante histiocitaria. Subscriber If you already have your login data, please click here. Inter Med, 41pp. Cir Pediatr, 13pp.

Enfermedad de Kikuchi-Fujimoto

The differential diagnosis of Kikuchi disease includes systemic lupus erythematosus SLEdisseminated tuberculosislymphomasarcoidosisand viral lymphadenitis. 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. se

It was first described by Dr Masahiro Kikuchi — in [6] and independently by Y. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

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A baciloscopia do escarro foi negativa. Acta Hematol Jpn ; A segunda paciente, de 58 anos, recebeu tratamento inicialmente para granulomatose de Wegener e, posteriormente, para tuberculose. Previous article Next article. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

CiteScore measures average citations received per document published. By using this site, you agree to the Terms of Use and Privacy Policy. Am J Clin Pathol,pp. SRJ is a prestige metric based on the idea that not all citations are the same.

Retrieved from ” https: Awareness of this disorder helps prevent ufjimoto and inappropriate treatment. Infobox medical condition new. Print Send to a friend Export reference Mendeley Statistics. The journal fully endorses the goals of updating knowledge and facilitating the acquisition of key developments in internal medicine applied to clinical practice.

Recognition of this condition is crucial, especially because it can easily be mistaken for tuberculosis, lymphoma, or even adenocarcinoma.