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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Enfermedad de Kikuchi-Fujimoto – Wikipedia, la enciclopedia libre

Annals of Pediatrics is the Body of Scientific Expression of the Association and is kjkuchi vehicle through which members communicate. The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Alguns autores descreveram 25 casos de DKF. Human leukocyte antigen class II genes are more frequent in patients with Kikuchi disease, suggesting a genetic predisposition to the proposed autoimmune response.

Si continua navegando, consideramos que acepta su uso. Cir Pediatr, 13pp. It is also known as histiocytic necrotizing lymphadenitis, Kikuchi necrotizing lymphadenitis, phagocytic necrotizing lymphadenitis, subacute necrotizing lymphadenitis, and necrotizing lymphadenitis. From Monday to Friday from 9 a. J Korean Med Sci. Si continua navegando, consideramos que acepta su uso. Nine issues are published each year, including mostly originals, reviews and consensus documents.

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D ICD – It is mainly a disease of young adults 20—30 yearswith a slight bias towards females. CiteScore measures average citations received per document published. J Otolaryngol Head Neck Surg. Symptomatic measures aimed at relieving the distressing local and systemic complaints have been described as the main line of management of KFD. The cause of this disease is not known, although infectious and autoimmune causes have been proposed.

Os exames laboratoriais kijuchi A new clinicopathological entity. An Med Int, 16pp. It was first described by Dr Masahiro Kikuchi — in [6] and independently by Y.

Enfermedad de Kikuchi-Fujimoto

Unusual systemic disorders associated with interstitial lung disease. Orphanet J Rare Dis. Os sinais e sintomas resolvem geralmente dentro de 4 meses. Pyrexia of unknown origin: You can change the settings or obtain more information by clicking here.

Micrograph of a lymph node with Kikuchi disease showing the characteristic features abundant histiocytesnecrosis without neutrophils. Enfermedad de Kikuchi o linfadenitis necrotizante histiocitaria. A pesquisa de BAAR foi negativa. Nonsteroidal anti-inflammatory drugs NSAIDs are indicated for tender lymph nodes and fever, and corticosteroids are useful in severe extranodal or generalized disease.

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The course of the disease is generally benign and self-limiting.

Kikuchi disease

Os exames laboratoriais revelaram: Orphanet J Rare Dis. Kikuchi disease or Kikuchi-Fujimoto disease was described in in Japan. Lymphadenitis showing focal reticulum cell hyperplasia with nuclear debris and phagocytes: Pediatrics,pp.

Mycobacterium szulgai and Yersinia and Toxoplasma species have been implicated.

Infobox medical condition new. Kikuchi-Fujimoto necrotizing lymphadenitis associated with brucellosis [Article in Spanish].

Alguns autores descreveram um caso de um paciente com DKF e tuberculose pulmonar concomitantes.

A baciloscopia do escarro foi negativa. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

Continuing navigation will be considered as acceptance of this use. Hospital Regional Universitario Infanta Cristina.