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Several episodes of acute hepatic enlargement associated with a dramatic fall in haemoglobin concentration were observed in two patients with sickle cell anaemia. No appreciable disturbances of liver function or signs of cardiac failure were evident. The most likely mechanism was sequestration of sickled erythrocytes in the liver. This complication, which may have a basis similar to that of splenic sequestration and the sickle lung syndrome, may be easily overlooked unless the size of the liver is regularly monitored in patients with sickle cell crisis.

More information Original publication

DOI

10.1136/bmj.290.6470.744

Type

Journal article

Publication Date

1985-03-09T00:00:00+00:00

Volume

290

Pages

744 - 745

Total pages

1

Keywords

Adolescent, Adult, Anemia, Sickle Cell, Erythrocytes, Abnormal, Female, Hemoglobins, Hepatomegaly, Humans, Liver, Radionuclide Imaging, Time Factors