A. Kedar et Rc. Braylan, Lymphohistiocytic anaplastic large cell lymphoma stage I: Long-term survival after resection alone, PED HEM ONC, 17(3), 2000, pp. 261-268
A 17-year-old female presented with axillary lymphadenopathy, which, on bio
psy, demonstrated an anaplastic large cell lymphoma of the lymphohistiocyti
c type (ALCL-LH). The tumor cells expressed the CD30 antigen and reacted wi
th the ALK1 antibody, suggesting the presence of the nucleophosminanaplasti
c large cell lymphoma kinase (NPM/ALK)fusion protein. No other adenopathy w
as found. Following a wide excision of the lymph node and without postopera
tive treatment, the patient remains free of disease 5 years later This case
demonstrates the potential curability of patients with early stages of ALC
L by local treatment.