2017, Number 4
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Med Int Mex 2017; 33 (4)
Kikuchi-Fujimoto disease
Córdova-Pluma VH, Vega-López CA, Alarcón-Sotelo A, Riancho-Guzmán JA, Almeida-Navarro JS, Salinas-Lezama E
Language: Spanish
References: 23
Page: 540-547
PDF size: 484.16 Kb.
ABSTRACT
Kikuchi-Fujimoto disease is a rare, self-limiting disease of unknown
etiology, manifested by lymphadenopathy, fever and less specific
symptoms such as nocturnal diaphoresis, weight loss, headache, fatigue,
nausea and arthralgias. The only way to establish the diagnosis
is through the histopathological findings, characterized by coagulative
necrosis with abundant remains of karyorrhexis in paracortical zones.
The treatment is symptomatic, and a differential diagnosis must be
made with infectious and neoplastic processes. We present the case
of a 37-year-old woman in whom the diagnosis of Kikuchi-Fujimoto
disease was integrated, and a review of the literature is made.
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