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%)