Histiocytic necrotizing lymphadenitis in the context of systemic lupus erythematosus (SLE): Is histiocytic necrotizing lymphadenitis in SLE associated with skin lesions?

Author:

Kim SK1,Kang MS2,Yoon BY3,Kim DY4,Cho SK5,Bae SC5,Her MY4

Affiliation:

1. Department of Internal Medicine, Arthritis and Autoimmunity Research Center, Catholic University of Daegu School of Medicine, Daegu, South Korea

2. Department of Pathology, Pusan Paik Hospital, Inje University, Busan, South Korea

3. Department of Internal Medicine, Ilsan Paik Hospital, Inje University, Goyang, South Korea

4. Division of Rheumatology, Department of Internal Medicine, Pusan Paik Hospital, Inje University, Busan, South Korea

5. Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, South Korea

Abstract

Histiocytic necrotizing lymphadenitis (HNL), or Kikuchi’s disease, is a benign and self-limiting lymphadenopathy that typically affects young Asian females. It presents with lymphadenopathy, usually cervical, accompanied by fever, chills and leukopenia. Although the association between systemic lupus erythematosus (SLE) and HNL is rare, the number of reports of HNL in SLE patients is increasing. We present nine cases of HNL in patients with SLE. Among the seven patients with diverse skin manifestations, three had skin manifestations that were histologically compatible with SLE. A review of previous reports in the literature showed that cutaneous involvement was commonly found in HNL in association with SLE. In the patients who had simultaneous onset of both diseases, lupus flare-ups were commonly observed. We suggest that HNL in SLE patients is associated with cutaneous manifestations. This report contributes to our understanding of the relationship between these diseases.

Publisher

SAGE Publications

Subject

Rheumatology

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