Development of Psoriatic Lesions

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    Development of psoriatic lesions. This figure depicts the transition from normal skin to fully

    developed lesion described in the text. Normal skin from a healthy individual ( panel A) contains

    epidermal Langerhans cells, scattered immature dendritic cells (D), and skinhoming memory T cells

    (T) in the dermis. Normalappearing skin from a psoriatic individual ( panel B) manifests slight

    capillary dilatation and curvature, and a slight increase in the numbers of dermal mononuclear cells

    and mast cells (!). " slight increase in epidermal thickness is usually present. #n chronic pla$ue

     psoriasis, the intensity of these changes may depend on distance from an established lesion. The

    transition %one of a developing lesion ( panel C) is characteri%ed by progressive increases in capillary

    dilatation and tortuosity, numbers of mast cells, macrophages (!&), and T cells, and mast cell

    degranulation (small arro's). #n the epidermis, there is increasing thickness 'ith increasingly

     prominent rete pegs, 'idening of the extracellular spaces, transient dyskeratosis, spotty loss of the

    granular layer, and parakeratosis. Langerhans cells (L) begin to exit the epidermis, and inflammatory

    dendritic epidermal cells (#) and D* T cells () begin to enter the epidermis. The fully developed

    lesion ( panel D) is characteri%ed by fully developed capillary dilatation and tortuosity 'ith a tenfold

    increase in blood flo', numerous macrophages underlying the basement membrane, and increased

    numbers of dermal T cells (mainly D+*) making contact 'ith maturing dermal dendritic cells (D).

    The epidermis of the mature lesion manifests markedly increased (approximately tenfold)

    keratinocyte hyperproliferation extending to the lo'er suprabasal layers, marked but not necessarilyuniform loss of the granular layer 'ith overlying compaction of the stratum corneum and

     parakeratosis, increased numbers of D* T cells, and accumulation of neutrophils in the stratum

    corneum (!unros microabscesses).

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