Volume 9, Issue 5 pp. 231-235
Original Article
Full Access

Cholecystosonography in children with sickle cell disease: Technical approach and clinical results

Jerome J. Cunningham MD

Corresponding Author

Jerome J. Cunningham MD

Departments of Radiology and Cell and Molecular Biology, Medical College of Georgia, Augusta

Department of Radiology, Medical College of Georgia, Augusta, GA 30912Search for more papers by this author
Stephen M. Houlihan BSRT

Stephen M. Houlihan BSRT

Departments of Radiology and Cell and Molecular Biology, Medical College of Georgia, Augusta

Search for more papers by this author
C. Altay MD

C. Altay MD

Departments of Radiology and Cell and Molecular Biology, Medical College of Georgia, Augusta

Search for more papers by this author
First published: June 1981
Citations: 14

Abstract

Forty-five children with sickle cell anemia were studied with meticulous cholecystosonograms using a 5-MHz thyroid transducer. Good-quality images were obtained. The most informative and useful view was the left-side-down decubitus study with the ultrasound gantry angled 45% to the anteroposterior axis. Rotating the patient rapidly through 360 degrees did not increase the information content of the examination. We found that one third of a random group of children with sickle cell anemia will have gallstones and one fifth will have “sludge”. A kinked deformity of the gallbladder may simulate a gallstone. Neither age, sex, weight, physical findings (except for hepatomegaly), nor a variety of biochemical measurements of the blood will be of much value in predicting gallbladder disease in any given patient.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.