Emergence of panniculitis and haemophagocytic syndrome in a patient with chronic systemic lupus erythematosus.

Abstract:

:Panniculitis rarely occurs in the course of systemic lupus erythematosus (SLE). When it occurs, it is thought to be mainly lupus erythematosus panniculitis (LEP). Here we describe a 32-year old Japanese woman with chronic SLE, who simultaneously presented facial lymphocytic lobular panniculitis and pancytopenia due to haemophagocytic syndrome. She showed several auto-antibodies against trilineage haematopoetic cells, an anti-cardiolipin antibody, and no evidence of viral infection, indicating that her haemophagocytic syndrome might be autoimmune-associated haemophagocytic syndrome. The panniculitis and haemophagocytic syndrome presented simultaneously, and these manifestations were dramatically improved with corticosteroid therapy; therefore, the lymphocytic lobular panniculitis could be linked to autoimmune-associated haemophagocytic syndrome in this case.

journal_name

Lupus

journal_title

Lupus

authors

Deji N,Sugimoto T,Fujimoto T,Aoyama M,Takeda N,Sakaguchi M,Uzu T,Kashiwagi A

doi

10.1177/0961203307077560

subject

Has Abstract

pub_date

2007-01-01 00:00:00

pages

363-5

issue

5

eissn

0961-2033

issn

1477-0962

pii

16/5/363

journal_volume

16

pub_type

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