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REPORT OF A CASE WITH AUTOPSY

ARTHUR S. ROSENFELD, M.D.; J. V. STRAUMFJORD, M.D.

Arch Intern Med. 1936;57(4):758-772.

	Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

The generic name lymphoblastoma cutis, suggested first by Mallory, in 1914, and later by Keim,¹ in 1924, covers a group of dyscrasias of the skin, glands and blood which blend one into the other and are of such rarity and interest as to warrant reporting them. In this group are included Hodgkin's disease, lymphosarcoma, leukemia and mycosis fungoides. Goeckerman stated that there is a growing tendency in this country to regard them as varying clinical manifestations of the same disease. At least, his experience at the Mayo Clinic supported the conception that the diseases are genetically closely related. In some cases a condition with characteristics of one disease has later changed and developed characteristics of another or possibly of several others of the group. Occasional mention of such metamorphoses has been made in the literature. According to Arndt,² Erhlich and his pupil Pinkus were the first to show . . . [Full Text PDF of this Article]

Author Affiliations
Assistant Professor Clinical Medicine, University of Oregon Medical School; Pathologist, Dr. R. C. Coffey Clinic and Hospital PORTLAND, ORE.

Footnotes
Read before the North Pacific Society of Internal Medicine, Seattle, March 17, 1934.

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