SPLENOMEGALY is a topic covered in the Harrison's Manual of Medicine.

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Just as the lymph nodes are specialized to fight pathogens in the tissues, the spleen is the lymphoid organ specialized to fight bloodborne pathogens. It has no afferent lymphatics. The spleen has specialized areas like the lymph node for making antibodies (follicles) and amplifying antigen-specific T cells (periarteriolar lymphatic sheath, or PALS). In addition, it has a well-developed reticuloendothelial system for removing particles and antibody-coated bacteria. The flow of blood through the spleen permits it to filter pathogens from the blood and to maintain quality control over erythrocytes (RBCs)—those that are old and nondeformable are destroyed, and intracellular inclusions (sometimes including pathogens such as Babesia and Plasmodium) are culled from the cells in a process called pitting. Under certain conditions, the spleen can generate hematopoietic cells in place of the marrow.

The normal spleen is about 12 cm in length and 7 cm in width and is not normally palpable. Dullness from the spleen can be percussed between the ninth and eleventh ribs with the pt lying on the right side. Palpation is best performed with the pt supine with knees flexed. The spleen may be felt because it descends when the pt inspires. Physical diagnosis is not sensitive. CT or ultrasound is a superior test.

Spleen enlargement occurs by three basic mechanisms: (1) hyperplasia or hypertrophy due to an increase in demand for splenic function (e.g., hereditary spherocytosis where demand for removal of defective RBCs is high or immune hyperplasia in response to systemic infection or immune diseases); (2) passive vascular congestion due to portal hypertension; and (3) infiltration with malignant cells, lipid- or glycoprotein-laden macrophages, or amyloid (Table 44-2). Massive enlargement, with spleen palpable >8 cm below the left costal margin, usually signifies a lymphoproliferative or myeloproliferative disorder.

TABLE 44-2: DISEASES ASSOCIATED WITH SPLENOMEGALY GROUPED BY PATHOGENIC MECHANISM
Enlargement Due to Increased Demand for Splenic Function

Reticuloendothelial system hyperplasia (for removal of defective erythrocytes)

 Spherocytosis

 Early sickle cell anemia

 Ovalocytosis

 Thalassemia major

 Hemoglobinopathies

 Paroxysmal nocturnal hemoglobinuria

 Pernicious anemia

Immune hyperplasia

 Response to infection (viral, bacterial, fungal, parasitic)

  Infectious mononucleosis

  AIDS

  Viral hepatitis

  Cytomegalovirus

  Subacute bacterial endocarditis

  Bacterial septicemia

  Congenital syphilis

  Splenic abscess

  Tuberculosis

  Histoplasmosis

  Malaria

 Leishmaniasis

 Trypanosomiasis

 Ehrlichiosis

Disordered immunoregulation

 Rheumatoid arthritis (Felty’s syndrome)

 Systemic lupus erythematosus

 Collagen vascular diseases

 Serum sickness

 Immune hemolytic anemias

 Immune thrombocytopenias

 Immune neutropenias

 Drug reactions

 Angioimmunoblastic lymphadenopathy

 Sarcoidosis

 Thyrotoxicosis (benign lymphoid hypertrophy)

 Interleukin-2 therapy

Extramedullary hematopoiesis

 Myelofibrosis

 Marrow damage by toxins, radiation, strontium

 Marrow infiltration by tumors, leukemias, Gaucher’s disease

Enlargement Due to Abnormal Splenic or Portal Blood Flow

Cirrhosis

Hepatic vein obstruction

Portal vein obstruction, intrahepatic or extrahepatic

Cavernous transformation of the portal vein

Splenic vein obstruction

Splenic artery aneurysm

Hepatic schistosomiasis

Congestive heart failure

Hepatic echinococcosis

Portal hypertension (any cause including the above): “Banti’s disease”

Infiltration of the Spleen

Intracellular or extracellular depositions

 Amyloidosis

 Gaucher’s disease

 Niemann-Pick disease

 Tangier disease

 Hurler’s syndrome and other mucopolysaccharidoses

 Hyperlipidemias

Benign and malignant cellular infiltrations

 Leukemias (acute, chronic, lymphoid, myeloid, monocytic, hairy cell)

 Lymphomas

Hodgkin’s lymphoma

Myeloproliferative syndromes (e.g., polycythemia vera, essential thrombocytosis)

Angiosarcomas

Metastatic tumors (melanoma is most common)

Eosinophilic granuloma

Histiocytic and dendritic cell neoplasms (Histiocytosis X)

Hamartomas

Hemangiomas, fibromas, lymphangiomas

Splenic cysts

Unknown Etiology

Idiopathic splenomegaly

Berylliosis

Iron-deficiency anemia

Peripheral blood RBC count, white blood cell count, and platelet count may be normal, decreased, or increased depending on the underlying disorder. Decreases in one or more cell lineages could indicate hypersplenism, increased destruction. In cases with hypersplenism, the spleen is removed and the cytopenia is generally reversed. In the absence of hypersplenism, most causes of splenomegaly are diagnosed on the basis of signs and symptoms and laboratory abnormalities associated with the underlying disorder. Splenectomy is rarely performed for diagnostic purposes.

Individuals who have had splenectomy are at increased risk of sepsis from a variety of organisms including pneumococcus and Haemophilus influenzae. Vaccines for these agents should be given before splenectomy is performed. Splenectomy compromises the immune response to T-independent polysaccharide antigens. Newer vaccine formulations are T dependent and are more effective in splenectomized persons.

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TY - ELEC T1 - SPLENOMEGALY ID - 623562 Y1 - 2017 PB - Harrison's Manual of Medicine UR - https://harrisons.unboundmedicine.com/harrisons/view/Harrisons-Manual-of-Medicine/623562/all/SPLENOMEGALY ER -