A 74-year-old Mexican man presented with an 18-month history of multiple, v
iolaceous, coalescing, firm, tender nodules with an ulcer in the anterior a
spect of the right leg (Fig. 1) and slightly infiltrated, ill-defined eryth
ematous plaques affecting the left leg and both forearms, He had not receiv
ed any treatment for his condition. Past medical history was relevant for n
oninsulin-dependent diabetes mellitus and hypertension without formal treat
ment and a history of heavy alcohol intake in his youth. A biopsy specimen
of both plaque-type lesions of the forearm and tumorous lesions of the leg
showed a diffuse, nonepidermotropic mononuclear infiltrate throughout the d
ermis and extending to the subcutis. The infiltrate was composed of pleomor
phic, atypical, large mononuclear cells (Fig. 2). Immunostaining with CD20
was positive for the atypical cells while CD3 was positive for normal appea
ring lymphocytes, characterized as reactive T cells. Additional laboratory
and image studies ruled out extracutaneous involvement. The diagnosis of pr
imary cutaneous large B cell lymphoma of the leg (LBCLL) was made. The pati
ent was initiated on radiotherapy localized to the right leg with a very go
od initial response nevertheless, resolution was not achieved and the plaqu
es in the rest of the limbs remained unchanged. Thus, the patient started c
hemotherapy with CHOP (Cyclophosphamide, Vincristine, Doxorubicin, Predniso
ne). He has currently finished his fourth cycle with this chemotherapy regi
men. The tumorous lesions involuted leaving only residual hyperpigmentation
(Fig. 3) and the plaques in the rest of the limbs disappeared, the area of
the ulcer diminished considerably. There is still no evidence of extracuta
neous involvement.