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Article
August 1956

Leiomyosarcoma of the Kidney: Report of a Case, with Review of the Literature

Author Affiliations

Miami Beach, Fla.
From the Departments of Surgery and Pathology of the Mount Sinai Hospital of Greater Miami.

AMA Arch Surg. 1956;73(2):346-352. doi:10.1001/archsurg.1956.01280020160029
Abstract

Leiomyosarcoma of the kidney is a relatively rare tumor. We have found 25 cases in the literature, which we have reviewed in the accompanying Table. We are presenting another case, with an attempt to clarify the biology of this type of tumor.

Report of a Case 

Present Illness.  —A 51-year-old white man was known to have had heart disease since 1946. After three years of angina pectoris, he developed what was considered to be a posterior wall infarct. In September, 1953, he was treated for advanced right and left ventricular failure. Since then, he had been maintained on digitalis and acetazoleamide (Diamox), and he continued to have recurrent angina. Recently, he noted pain in the right upper quadrant, occurring more often at rest than on exertion and unrelated to dietary indiscretion. The pain radiated into the chest, right shoulder, and right scapular region. He entered the Mount Sinai Hospital on

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