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PRIMARY neoplasms of the large or small intestine are extremely rare in childhood as compared with those in adult life. Except for true adenomatous polyps, most intestinal tumors encountered in early life are sarcomatous. Lymphosarcoma is one of the more frequent types of this group, and it is the purpose of this paper to describe our experience with this tumor in children under twelve years of age, as well as a case of reticulum-cell sarcoma.PathologyLymphosarcoma was separated from the general group of lymphoma in 1893 by Kundrat,1 who described it as a highly malignant tumor of lymphoid tissue . . .
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Cutler et al. (1945) studied this question.
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