C. Martinezvazquez et al., HISTIOCYTIC NECROTIZING LYMPHADENITIS, KIKUCHI-FUJIMOTOS-DISEASE, ASSOCIATED WITH SYSTEMIC LUPUS ERYTHEMOTOSUS, Quarterly Journal of Medicine, 90(8), 1997, pp. 531-533
Histiocytic necrotizing lymphadenitis, Kikuchi-Fujimoto's Disease (KFD
), is a condition rarely associated with systemic lupus erythematosus
(SLE). The diagnosis of KFD can precede, postdate or coincide with the
diagnosis of SLE. Lymphadenopathy is a common clinical presentation o
f KFD and SLE, and is histologically indistinguishable in both conditi
ons. We describe two cases of KFD associated with SLE. The diagnosis o
f KFD in one case was made several years before the diagnosis of SLE,
and the other was simultaneous. Both showed large lymphadenopathy, but
neither fever nor neutropenia. Lymph-node biopsy showed necrosis, wit
h proliferation of histiocytes and immunoblasts, paucity of neutrophil
s and absence of hemathoxilin bodies. Both patients responded favourab
ly to steroid treatment. Patients with KFD should be assessed for SLE
and have long-term follow-up checking for development of SLE. KFD shou
ld be ruled out in SLE flare-up accompanied by lymphadenopathy.