ENFERMEDAD DE KIKUCHI FUJIMOTO PDF

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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Pediatrics,pp. Acta Haematol, 35pp. Previous article Next article. KFD may represent an exuberant T-cell -mediated immune response in a genetically susceptible individual to a variety of nonspecific stimuli.

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Exames laboratoriais mostraram FAN 1: Print Send to a friend Export reference Mendeley Statistics. Kikuchi-Fujimoto disease KFD is a rare, self-limiting disorder that typically affects the cervical lymph nodes. A baciloscopia do escarro foi negativa.

Cir Pediatr, 13pp. How to cite this article.

The cause of this disease is not known, although infectious and autoimmune causes have been proposed. Lymph node enlargmeent usually resolves over several weeks to six months. D Fujimofo – Are you a health professional able to prescribe or dispense drugs? SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

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Services on Demand Journal. Abscess of thymus Thymus hyperplasia. Aetiology of peripheral lymphadenopathy in adults: Curr Opin Pulm Med.

encermedad Subscribe to our Newsletter. This item has received. UpToDate [cited Aug, version From Monday to Friday from 9 a.

Proc Bayl Univ Med Cent. It is also known as histiocytic necrotizing lymphadenitis, Kikuchi necrotizing lymphadenitis, phagocytic necrotizing lymphadenitis, subacute necrotizing lymphadenitis, and necrotizing lymphadenitis.

You can change the settings or obtain more information by clicking here. 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. Retrieved 17 April Enfermfdad to our Newsletter. An Med Int, 16pp.

Enfermedad de Kikuchi-Fujimoto

The differential diagnosis of Kikuchi disease includes systemic lupus erythematosus SLEdisseminated tuberculosislymphomasarcoidosisand viral lymphadenitis. J Otolaryngol Head Neck Surg. Alguns autores descreveram 25 casos de DKF.

Nine issues are published each year, including mostly originals, reviews and consensus documents. Acta Hematol Jpn ; Nonsteroidal anti-inflammatory drugs NSAIDs are indicated for tender lymph nodes and fever, and corticosteroids are useful in severe extranodal or generalized disease. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

Med Clin Barc, pp. Retrieved from ” https: Entretanto, a idade dos pacientes pode variar de 6 a 80 anos. Lymphadenitis showing focal reticulum cell hyperplasia with nuclear debris and phagocytes: US and CT apperance. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

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Pyrexia of unknown origin: Orphanet J Rare Dis.

Si continua navegando, consideramos que acepta su uso. Recognition of this condition is crucial, especially because it can easily be mistaken for tuberculosis, lymphoma, or even adenocarcinoma. 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. Kikuchi-Fujimoto necrotizing kkuchi associated with brucellosis [Article in Spanish].

KFD is now proposed to be a nonspecific hyperimmune reaction to a variety of infectious, chemical, physical, and neoplastic agents.

Treatment is largely supportive. Human leukocyte antigen class II genes are more frequent in patients with Kikuchi disease, suggesting a genetic predisposition to the proposed autoimmune response. Full text is only aviable in PDF.

Subscriber If you already have your login data, please click here. It is mainly a disease of young adults 20—30 yearswith a slight bias towards females. A new clinicopathological entity.