Часті причини спленомегалії

Type

Examples

Chronic hemolytic anemia

Hemoglobinopathies, including the thalassemias, sickle cell hemoglobin variants (eg, hemoglobin S-C disease, sickle/beta thalassemia), and congenital Heinz body hemolytic anemias

Red blood cell enzymopathies (eg, pyruvate kinase deficiency)

Red blood cell shape abnormalities (eg, hereditary spherocytosis, hereditary elliptocytosis)

Congestive

Certain vascular malformations or thrombosis of the portal venous vasculature

Cirrhosis

External compression of portal or splenic veins

Infectious and inflammatory

Acute infections (eg, infectious hepatitis, infectious mononucleosis, psittacosis, subacute bacterial endocarditis)

Chronic infections (eg, bartonellosis, brucellosis, candidiasis, histoplasmosis, malaria, miliary tuberculosis, visceral leishmaniasis [kala-azar], syphilis)

Connective tissue disorders (eg, rheumatoid arthritis with Felty syndrome), systemic lupus erythematosus

Hemophagocytic lymphohistiocytosis

Langerhans cell histiocytosis

Sarcoidosis

Secondary amyloidosis

Myeloproliferative and lymphoproliferative

Leukemias, especially chronic lymphocytic, large granular lymphocytic, and chronic myelogenous leukemia

Lymphomas, especially hairy cell leukemia and splenic marginal zone lymphoma

Primary myelofibrosis

Polycythemia vera

Storage diseases

Gaucher disease

Niemann-Pick disease

Wolman disease

Structural

Splenic cysts, usually caused by resolution of previous intrasplenic hematoma

Adapted from Williams WJ, et al: Hematology. New York, McGraw-Hill Book Company, 1976.

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