Necrotizing lymphadenitis: Kikuchi—Fujimoto disease alias lupus lymphadenitis?

Author:

Cramer JP1,Schmiedel S.1,Alegre NG2,Schäfer H.3,Burchard GD1,Merz H.4

Affiliation:

1. Section for Tropical Medicine, I, Department of Internal Medicine, University Medical Centre Hamburg-Eppendorf, Bernhard-Nocht-Strasse 74, 20359 Hamburg, Germany

2. Chinese General Hospital and Medical Center, Manila, Philippines

3. Institute for Pathology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany

4. German Consultation and Reference Centre for Lymphomas, Institute of Pathology, University Medical Centre Schleswig-Holstein, Luebeck, Germany,

Abstract

Differentiation between lymphadenopathy in potentially life-threatening systemic lupus erythematosus (SLE) and self-limiting necrotizing lymphadenitis, also called Kikuchi— Fujimoto disease (KFD), is difficult. In the past, co-occurrence of SLE and KFD has been described repeatedly in case reports. Here, we report a case of necrotizing lymphadenitis, describe the clinical and histopathologic features in detail and discuss the current literature. KFD may in fact be a histopathologic characteristic of SLE supporting the hypothesis that KFD is a rare manifestation of SLE. To clarify whether KFD is the same entity as lupus lymphadenitis, more cases with SLE and lymphadenopathy should be examined in detail. Lupus (2010) 19, 89—92.

Publisher

SAGE Publications

Subject

Rheumatology

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