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Kikuchi Fujimato Disease

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dc.contributor.authorErtas, Burak
dc.contributor.authorVeyseller, Bayram
dc.contributor.authorAksoy, Fadlullah
dc.contributor.authorÖZTURAN, ORHAN
dc.contributor.authorBarutcu, Saime Gul
dc.contributor.institutionauthorAKSOY, FADLULLAH
dc.contributor.institutionauthorÖZTURAN, ORHAN
dc.date.accessioned2020-10-22T18:37:25Z
dc.date.available2020-10-22T18:37:25Z
dc.date.issued2013-12-01T00:00:00Z
dc.description.abstractKikuchi Fujimato disease (KFD) also know as histiocytic necrotizing lymphadenitis (HNL) is a benign, self limiting disease, which commonly affects young women under 30 years of age. Most of the cases resolve in a six month period. Laboratory and clinical findings of KFD show similarities with tuberculosis lymphadenitis, mailgn lymphoma, other malign and benign diseases. The diagnosis is established on the basis of histology of lymph node excisional biopsy. The differentiation of KFD from Sistemik Lupus Eritematosus (SLE) can sometimes be problematic because both can show similar clinical and histological features. KFD and SLE can be seen together. Forty two years-old female patient diagnosed with KFD was discussed in light of current literature.
dc.identifier.citationErtas B., Veyseller B., Aksoy F., ÖZTURAN O., Barutcu S. G. , -Kikuchi Fujimato Disease-, TURKISH ARCHIVES OF OTORHINOLARYNGOLOGY-TURK OTORINOLARENGOLOJI ARSIVI, cilt.51, ss.135-137, 2013
dc.identifier.doi10.5152/tao.2013.1388
dc.identifier.trdizintrdizin
dc.identifier.urihttp://hdl.handle.net/20.500.12645/24271
dc.identifier.wosWOS:000421054700009
dc.titleKikuchi Fujimato Disease
dc.typeArticle
dspace.entity.typePublication
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local.publication.goal03 - Sağlık ve Kaliteli Yaşam
local.publication.isinternational1
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relation.isGoalOfPublication.latestForDiscovery9c198c48-b603-4e2f-8366-04edcfc1224c
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