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primaire cutane plasmocytose (aandoening)
primaire cutane plasmocytose
Primary cutaneous plasmacytosis
A rare acquired skin disease characterized by benign proliferation of mature plasma cells with a typical triad of cutaneous lesions, polyclonal hypergammaglobulinemia and superficial lymphadenopathy without an apparent underlying cause. The skin lesions consist of multiple round-to-oval, red-to-dark-brown macules, papules and plaques most commonly found on the trunk but also the face, neck, and axilla.
Id1228842003
StatusPrimitive
Associated morphologyafwijkend weefsel
Finding sitestructuur van huid
Occurrencelevensperiode tussen geboorte en dood
Pathological processafwijkend immuunproces
SNOMED CT to Orphanet simple map451602
SNOMED CT to ICD-10 extended map
TargetL98.6
RuleTRUE
AdviceALWAYS L98.6 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified