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Article
March 1965

Hemangioma of the Spleen

Author Affiliations

CHARLOTTESVILLE, VA

From the departments of internal medicine and surgery, University of Virginia Hospital and School of Medicine. Resident (Dr. Benjamin) and Assistant Professor (Dr. Mohler), Department of Internal Medicine; Professor, Department of Surgery (Dr. Sandusky).

Arch Intern Med. 1965;115(3):280-284. doi:10.1001/archinte.1965.03860150024005
Abstract

PRIMARY tumors of the spleen are rare and with the exception of malignant lymphoma are seldom considered in the differential diagnosis of splenomegaly. Such tumors may be either cystic or solid, and the cystic variety, composed mostly of epidermoid cysts, has occurred with slightly greater frequency.1 The most common primary solid tumor is the hemangioma (hamartoma) and the majority of these have been described as incidental autopsy findings.2,3 Thirty-nine hemangiomas have been reported because of their clinical manifestations.4 This report describes a case that illustrates some of the features common to this tumor and also demonstrates for the first time the results of radioisotopic scanning of a primary splenic neoplasm.

Report of Case  A 29-year-old white nurse was admitted to the University of Virginia Hospital in September 1963 for evaluation of unexplained splenomegaly. At the age of 19 she was told she had mild anemia and was

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