Relapse in Burkitt's lymphoma.

dc.contributor.authorNkrumah, F.K.
dc.contributor.authorPerkins, I.V.
dc.date.accessioned2013-06-20T13:05:11Z
dc.date.accessioned2017-10-16T13:15:43Z
dc.date.available2013-06-20T13:05:11Z
dc.date.available2017-10-16T13:15:43Z
dc.date.issued1976
dc.description.abstractOf 109 patients with histologically confirmed Burkitt's lymphoma who completed a course of chemotherapy, 86 (79%) achieved complete remission. Forty-five (52%) of patients with initial complete remission relapsed with tumour over an observation period ranging from 2 years to over 5 years. Relapse was more common in patients who initially presented with abdominal or central nervous system (CNS) involvement than in patients who presented with localized facial tumours (p<0.01). Anatomical distribution of tumour on relapse differed from that at presentation. Facial bones were much less frequently involved on relapse; on the other hand, the CNS, cranial nerves, orbits and skin were frequent sites of disease on relapse. CNS involvement occurred in 42% (19/45) of patients at the first relapse and in 73% (11/15) of patients with multiple relapses. Prognosis in these patients was poor. Two relapse types were clinically identifiable. Early relapse (remission duration<12 weeks) was associated with frequent involvement of the CNS, drug resistance and a generally unfavourable outcome. Patients with late relapse (remission duration >12 weeks) responded much better to secondary treatment. Possible pathogenic mechanisms underlying these two relapse types are discussed.en_US
dc.identifier.citationNkrumah, F. K., & Perkins, I. V. (1976). Relapse in Burkitt's lymphoma. International Journal of Cancer, 17(4), 455-460.en_US
dc.identifier.urihttp://197.255.68.203/handle/123456789/3743
dc.language.isoenen_US
dc.publisherInternational Journal of Canceren_US
dc.titleRelapse in Burkitt's lymphoma.en_US
dc.typeArticleen_US

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