Subacute
cutaneous lupus erythematosus
This
is less severe than acute SLE, but is also often associated with systemic
disease. Its cause is unknown, but probably involves an antibody-dependent
cellular cytotoxic attack on basal cells by K cells bridged by antibody to Ro
(SS-A) antigen.
Patients with subacute cutaneous LE are often photo-sensitive. The skin lesions are sharply marginated scaling psoriasiform plaques, sometimes annular, lying on the forehead, nose, cheeks, chest, hands and extensor surfaces of the arms. They tend to be sym-metrical and are hard to tell from discoid LE, or SLE with widespread discoid lesions.
As
in SLE, the course is prolonged. The skin lesions are slow to clear but, in
contrast to discoid LE, do so with little or no scarring.
Systemic
disease is frequent, but not usually serious. Children born to mothers who
have, or have had, this condition are liable to neonatal LE with transient
annular skin lesions and permanent heart block.
The
morphology is characteristic, but lesions can be mistaken for psoriasis or
widespread discoid LE. Annular lesions may resemble tinea corporis or figurate erythemas.
Patients
with subacute cutaneous LE should be evaluated in the same way as those with
acute SLE, although deposits of immunoglobulins in the skin and antinuclear
antibodies in serum are present less often. Many have antibodies to the
cytoplasmic antigen Ro (SS-A).
Subacute
cutaneous LE does better with antimalarials, such as hydroxychloroquine, than
acute SLE. Oral retinoids are also effective in some cases. Systemic steroids
may be needed too.
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