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Kimura disease: review of the literature.
Sun, Q-F; Xu, D-Z; Pan, S-H; Ding, J-G; Xue, Z-Q; Miao, C-S; Cao, G-J; Jin, D-J.
Afiliación
  • Sun QF; Department of Infectious Diseases, The Third Affilated Hospital to Wenzhou Medical College, Wenzhou, Zhejiang, China. sunxue0806@126.com
Intern Med J ; 38(8): 668-72, 2008 Aug.
Article en En | MEDLINE | ID: mdl-18808562
Kimura disease (KD) is a rare, chronic inflammatory disease of unknown cause and is characterized by painless s.c. swellings and lymphadenopathy commonly affecting the head and neck region. Much therapeutics has been used to treat KD, but is not satisfactory because of frequent relapse. Imatinib has been reported previously to be useful for treatment of hypereosinophilic syndrome and may work by selectively blocking protein-tyrosine kinases, such as platelet-derived growth factor receptor, and c-Kit. We carried out immunohistochemical examination of platelet-derived growth factor receptor-alpha and c-Kit in tissues from patients with KD. The results were positive and suggested that Imatinib might be an effective drug for the treatment of the disease. We have also briefly reviewed the epidemiology, aetiology, clinical manifestations, laboratory and pathological examinations, differential diagnoses, treatment and prognosis of KD in this manuscript.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hiperplasia Angiolinfoide con Eosinofilia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Intern Med J Asunto de la revista: MEDICINA INTERNA Año: 2008 Tipo del documento: Article País de afiliación: China Pais de publicación: Australia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hiperplasia Angiolinfoide con Eosinofilia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Intern Med J Asunto de la revista: MEDICINA INTERNA Año: 2008 Tipo del documento: Article País de afiliación: China Pais de publicación: Australia