Hypersplenism
A syndrome marked by exaggerated splenic activity and, possibly, splenomegaly, hypersplenism causes peripheral blood cell deficiency as the spleen traps and destroys these cells.
In this disorder, the spleen’s normal filtering and phagocytic functions accelerate indiscriminately, automatically removing antibody–coated, aging, and abnormal cells, even though some cells may be functionally normal. The spleen may also temporarily sequester normal platelets and red blood cells (RBCs), withholding them from circulation. In this manner, the enlarged spleen may trap as much as 90% of the body’s platelets and up to 45% of its RBC mass.
Causes
Hypersplenism may be idiopathic (primary) or secondary to an extrasplenic disorder, such as malaria or polycythemia vera. (See What causes splenomegaly?)
What causes splenomegaly?
An enlarged spleen may develop in any of the disorders listed below.
Infectious disorders
Acute (abscesses, subacute bacterial endocarditis); chronic (tuberculosis, malaria, Felty’s syndrome)
Congestive disorders
Cirrhosis, thrombosis
Hyperplastic disorders
Hemolytic anemia, polycythemia vera
Infiltrative disorders
Gaucher’s disease, NiemannPick disease
Cystic or neoplastic disorders
Cysts, leukemia, lymphoma, myelofibrosis, Hodgkin’s disease, multiple myeloma
Complications
Infection, anemia, and hemorrhage can complicate hypersplenism.