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Familial chilblain lupus erythematosus (disorder)
Familial chilblain lupus erythematosus
A rare monogenic form of cutaneous lupus erythematosus characterized by infantile or childhood onset of cold-induced erythematous papules or plaques predominantly on the fingers, toes, nose, cheeks, and ears. Recurrent ulceration of the lesions may lead to necrotic tissue destruction and mutilation. Patients may experience ischemia of the affected acral regions. Histological findings include cutaneous perivascular inflammatory infiltrates with deposits of immunoglobulins or complement.
Id1220590003
StatusPrimitive
Finding siteSkin structure
Pathological processAutoimmune process
Clinical courseChronic
ICD-10 complex map reference set
TargetL93.2
RuleTRUE
AdviceALWAYS L93.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified