By Disease Name > Pseudolymphoma > Cutaneous B-Cell Pseudolymphoma

Cutaneous B-Cell Pseudolymphoma

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AKA lymphocytoma cutis; cutaneous lymphoid hyperplasia; Speigler-Fendt sarcoid
most cases, cause unknown
clinically = purple plum
face, chest, and upper extremities

 

histology:

by definition, composed of nodular collections of mature B lymphocytes
infiltrate tends to favor papillary dermis (“top heavy”)
+/- germinal centers
features favoring malignancy:
monomorphous infiltrate with atypical cells
epidermal, adnexal and vascular infiltration
“bottom heavy” pattern of infiltration
dissection of lymphoid cells between collagen bundles
poor circumscription of lymphoid aggregates
necrosis
features favoring a benign diagnosis
a patchy rather than a heavy diffuse infiltrate
germinal centers containing “tingible body” macrophages

 

Immunohistochemistry:

Borrelial Lymphocytoma Cutis

rare in N. America
distribution classically: earlobe, areola, nose, scrotum (i.e. low skin temperature)
especially children
check serum antibody titer of B. burgdorferi (elevated in 50%)