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S1C30P20-1a & b: The eosinophil is a specialized cell with distinctive, acidophilic, cytoplasmic granules. The granules are larger and more acidophilic than those of a neutrophil; the nucleus of an eosinophil is
usually bi-lobed. This special cell is a store of catalytic enzymes and toxic proteins. It may secrete the stored products or, by disintegrating, release its granules into the interstitium. It is a migratory cell
with a special affinity for allergic reactions. It is often emphasized as a significant reacting cell in helminth infestations, and is a common component of the infiltrates associated with arthopod bites, scabies,
and eosinophilic cellulitis (Well’s syndrome). It is variably represented in the infiltrates of many drug eruptions, including interstitial disorders such as eosinophilic fasciitis (Shuman’s syndrome). It is also
found in variable numbers in the infiltrates of nummular eczema. It may be found in both dermal and epidermal infiltrates in disorders such as bullous pemphigoid, or pemphigus. In epidermal infiltrates, eosinophils
often are associated with intercellular edema and intraepidermal vesicles (eosinophilic spongiosis). Edema and eosinophilic infiltrates go hand in hand; in a temporal sequence, histiocytes commonly follow
eosinophils. If not for the contributions of “molecular pathologists,” it might be tempting to attribute the relationship between eosinophil-rich infiltrates and aggregated histiocytes to the insolubility of the
products of eosinophils. In the above illustrations, the patterns in the epidermis are psoriasiform and spongiotic vesicular. The papillary dermis is widened and edematous. The presence of eosinophils
in the infiltrates qualifies the reaction as eosinophilic spongiosis. This is a generic category which includes, among other options, harbingers of either bullous pemphigoid or pemphigus. Other disorders may
occasionally present as an eosinophilic spongiosis only to be revealed as a more specific disorder at a later date.
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