Kikuchi-Fujimoto Disease in Patients with Sjögren’s Syndrome

DOI: 10.4236/ojpathology.2013.31006   PDF   HTML   XML   3,692 Downloads   6,455 Views   Citations

Abstract

Sjogren’s syndrome is a chronic autoimmune exocrinopathy associated with dry eyes and dry mouth as major clinical manifestations. It is characterized by lymphocytic infiltration of lacrimal and salivary glands and autoantibody production, especially anti-Ro (or SSA) and anti-La (or SSB). Lymphoproliferative disorders are a feature of Sjogren’s syndrome, and can be considered an extraglandular manifestation of the disease. Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis is a rare form of lymphadenitis. It is reported more often in young adult women with localized lymphadenopathy (usually cervical), fever, rashes, and leukopenia. It is a self-limiting disease with resolution within 1 - 4 months in almost all patients. Sjogren’s syndrome has been reported in patients with other systemic diseases including SLE and lymphomas. Here we present a patient with Kikuchi-Fujimoto disease who developed Sjogren’s Syndrome 8 years after her diagnosis of Kikuchi-Fujimoto disease.

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L. Radfar, M. Radfar, K. Moser and R. Scofield, "Kikuchi-Fujimoto Disease in Patients with Sjögren’s Syndrome," Open Journal of Pathology, Vol. 3 No. 1, 2013, pp. 32-36. doi: 10.4236/ojpathology.2013.31006.

Conflicts of Interest

The authors declare no conflicts of interest.

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