Childhood lymphoma as commonly observed in certain areas of Africa and conveniently labelled “Burkitt tumor,” was diagnosed in 35 cases during 6 years (1958–63 incl.) in the Territories of Papua and New Guinea (population about 2,000,000) and was the most commonly reported childhood malignancy. The clinical and pathological features of these cases followed closely the descriptions from Africa but distinct geographical and climatic limitations were not observed. Sex ratio, age‐grouping and reversal of lymphoma‐leukemia ratio all showed remarkable similarity with the African observations but jaw tumors formed only one third of the cases. The difficulty of identifying tumors from an etiological viewpoint even when clinical and pathological presentation are similar, has been discussed. At present it does not seem possible to declare the Burkitt tumor to be a definite entity.