[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 18.207.134.98. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
August 1956

SPLENIC INFARCTION IN A PATIENT WITH SICKLE-CELL-HEMOGLOBIN-C DISEASE: Report of a Case Occurring Following Air Travel

Author Affiliations

Rochester, N. Y.

From the Department of Medicine, University of Rochester School of Medicine and Dentistry. Instructor in Medicine (Dr. Coleman); Special Fellow, U. S. P. S., National Heart Institute (Dr. Furth).

AMA Arch Intern Med. 1956;98(2):247-249. doi:10.1001/archinte.1956.00250260121012
Abstract

SULLIVAN,1 in 1950, reported the occurrence of splenic infarction after air travel in a Negro whose erythrocytes exhibited the sickling phenomenon. Since 1950 a number of cases of splenic infarction in association with air travel in sicklemics have been reported.* By means of electrophoretic studies of the hemoglobin, it has been established that this type of infarction may occur in Negroes having either sickle-cell trait or sickle-cell-hemoglobin-C disease.5 From previous reports, it appears that exposure to altitudes above 10,000 feet is required for splenic infarction to occur in persons with sickle-cell trait but that splenic infarction can occur in association with sickle-cell-hemoglobin-C disease upon exposure to altitudes abve 5000 feet.† All of the previously reported cases have been males, principally men in military service. The case reported here is that of a young Negro woman with sickle-cell-hemoglobin-C disease who developed splenic infarction during a commercial air flight.

Report 

×