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  Vol. 106 No. 6, DECEMBER 1960 TABLE OF CONTENTS
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Intrathoracic Plasmacytoma

Report of a Case and Review of the Literature

KAYE H. KILBURN, M.D.; ALEXANDER M. SCHMIDT, M.D.

Arch Intern Med. 1960;106(6):862-869.

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 common diagnostic possibilities when a mediastinal or hilar mass is discovered in the absence of parenchymal pulmonary disease can be divided into diseases of mediastinal structures and diseases of lymph nodes. The former group includes benign cysts, dermoid cysts, teratomas, tumors of the thyroid and thymus, and tumors of neural origin and of connective tissue.1 The common causes of hilar or mediastinal lymph node enlargement are granulomas, lymphomas, and metastatic carcinoma, while reactive hyperplasia, erythema nodosum, sarcoidosis, and leukemia virtually comprise the less common causes. Plasma-cell tumors of the hilar nodes are unusual members of this latter group.

The discovery of a plasma-cell tumor in a large hilar node of an asymptomatic 47-year-old man provoked this review of the life history and significance of extramedullary plasma-cell tumors located within the chest, and particularly of their relationship to multiple myeloma.

Report of Case

A 47-year-old white laborer was admitted . . . [Full Text PDF of this Article]


Author Affiliations

Salt Lake City

From the Veterans Administration Hospital and Department of Medicine of the University of Utah College of Medicine, Salt Lake City.


Footnotes

Submitted for publication Jan. 4, 1960.

Present address (Dr. Kilburn): U.S. Army Medical Research and Nutrition Laboratory, Fitzsimons General Hospital, Denver (30).



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