Sweet syndrome – low magnification
LEGEND
There is no true leukocytoclastic vasculitis (no fibrinoid necrosis), but neutrophilic debris and possible endothelial swelling may be observed.
Significant papillary dermal edema may be present, and if severe, can lead to a subepidermal blister. Red blood cell extravasation is noted.
The epidermis is variable. In this case, there is mild spongiosis in response to a few migrating cells in the epidermis
Interstitial dermal infiltrate of neutrophils with some lymphocytes, histiocytes, and eosinophils
Sweet syndrome – high magnification
LEGEND
Diffuse and interstitial dermal infiltrate of neutrophils with neutrophilic debris
Red blood cell extravasation
Sweet syndrome – low magnification
LEGEND
There are several variants of Sweet syndrome. This one is the histiocytoid variant.
Histiocytoid Sweet is not a form of Sweet syndrome that includes histiocytes in the infiltrate, but rather immature myeloid cells (neutrophils) that are large and have non-lobulated nuclei, making them resemble histiocytes
Due to these immature myeloid cells, histiocytoid Sweet must be differentiated from leukemia cutis
The presence of histiocytoid Sweet increases the likelihood that the Sweet syndrome is secondary to a myeloproliferative disorder.
Classic finding: edema in the papillary dermis
Diffuse and interstitial dermal infiltrate of neutrophils with some lymphocytes, histiocytes, and eosinophils
Sweet syndrome – high magnification
LEGEND
Presence of significant edema in the papillary dermis
Variable epidermis; in this case, mild spongiosis in response to migrating cells
Histiocytoid variant
LEGEND
MPO (myeloperoxidase) positive, confirming myeloid lineage
CD68 positive