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  Vol. 102 No. 5, NOVEMBER 1958 TABLE OF CONTENTS
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Sarcoidosis

Clinical Observation on One Hundred Sixty Cases

HAROLD L. ISRAEL, M.D.; MAURICE SONES, M.D.

AMA Arch Intern Med. 1958;102(5):766-776.

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

Sarcoidosis can no longer be regarded as a rare disease. A recent investigation disclosed 1194 cases of this disease in Veterans' Administration Hospitals in a five-year interval,1 and chest x-ray surveys of 1,000,000 inhabitants of Sweden between 1950 and 1954 detected almost half as many cases of sarcoidosis as of tuberculosis.2 Whether these impressive numbers of cases are merely the result of better recognition or whether sarcoidosis is actually increasing in prevalence remains to be determined. In either event, because of its growing importance, sarcoidosis is a disease with which all physicians should be familiar.

Reported here are observations in 160 patients who came under our observation between 1938 and 1956, in clinic, hospital, or office practice. All cases included in this series had one or more biopsies demonstrating epithelioid tubercles.

The age and sex distribution of these patients, shown in Table 1, is typical of that observed . . . [Full Text PDF of this Article]


Author Affiliations

Philadelphia

From the Graduate School of Medicine and the Henry Phipps Institute of the University of Pennsylvania, and from the Woman's Medical College of Pennsylvania.


Footnotes

Submitted for publication March 5, 1958.

Presented at the annual Clinical Meeting, American Medical Association, Philadelphia, Dec. 4, 1957.

Aided by a medical research grant from the National Tuberculosis Association through its medical section, the American Trudeau Society.



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