Splenomegaly causes

Template:Splenomegaly Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]

Overview

The causes of splenomegaly vary widely and range from infections, congestion due to increased blood flow, Cirrhosis and other liver diseases, infiltration of the spleen from other diseases like Leukemia, Lymphoma and storage disorders, inflammatory conditions like Sarcoidosis and Lupus, blood cell diseases and Malignancies.

Causes

Common causes of Splenomegaly

• Bacterial endocarditis
• Infectious mononucleosis
• Cirrhosis
• Congestive heart failure
• Leukemia
• Long standing alcohol abuse
• Lymphoma
• Malaria
• Portal hypertension 
• Sickle cell anemia
• Spherocytosis
• Thalassemia

Causes by Pathogenesis

Increased function	Abnormal blood flow	Infiltration
Removal of defective RBCs Spherocytosis Thalassemia Hemoglobinopathies Nutritional anemias sickle cell anemia Immune hyperplasia Response to infection (viral,bacterial,fungal,parasitic) Mononucleosis, AIDS, Viral hepatitis Subacute bacterial endocarditis, Bacterial septicemia Splenic abscess, Typhoid fever brucellosis,Leptospirosis, tuberculosis Histoplasmosis Malaria, leishmaniasis, trypanosomiasis Ehrlichiosis Disordered immunoregulation Rheumatoid arthritis SLE Serum sickness Autoimmune hemolytic anemia Immune thrombocytopenia Sarcoidosis Drug reactions Extramedullary hematopoiesis Myelofibrosis Marrow infiltration by tumors, leukemias marrow damage by radiation, toxins	Organ Failure Cirrhosis congestive heart failure Vascular Hepatic vein obstruction Portal vein obstruction Budd-Chiari syndrome Splenic vein obstruction Infections Hepatic schistosomiasis Hepatic echinococcosis	Metabolic diseases Gauchers disease Niemann-Pick disease Hurler syndrome and other Mucopolysaccharidoses Amyloidosis Tangier disease Benign and malignant infiltrations Leukemias(acute, chronic, lymphoid and myeloid) Lymphomas (Hodgkins and non-hodgkins) Myeloproliferative disorders Metastatic tumors(commonly melanoma) Histiocytosis X Hemangioma,Lymphangioma Splenic cyst Hamartomas Eosinophilic granuloma

Causes of Massive Splenomegaly (>1000 gms)

• Autoimmune hemolytic anemia
• Chronic lymphocytic leukemia
• Chronic myelogenous leukemia
• Gauchers disease
• Hairy cell leukemia
• Kala-Azar (Leishmaniasis)
• Lymphomas
• Malaria
• Myelofibrosis
• Polycythemia vera
• Portal hypertension of Bilharziasis
• Sarcoidosis
• Thalassemia

Less Common Causes

• Amyloidosis
• Babesiosis
• Gaucher's disease
• Histoplasmosis
• Kala-azar
• Rickets
• Schistosomiasis
• Syphilis
• Toxoplasmosis
• Typhoid fever

Causes by Organ System

Cardiovascular	Congestive heart failure, Constrictive pericarditis, Infective endocarditis
Chemical/Poisoning	No underlying causes
Dental	No underlying causes
Dermatologic	No underlying causes
Drug Side Effect	Cidofovir, Filgrastim
Ear Nose Throat	No underlying causes
Endocrine	Thyrotoxicosis
Environmental	No underlying causes
Gastroenterologic	Cirrhosis, Cruveilhier-Baumgarten syndrome, Hepatic portal vein obstruction, Hepatic vein thrombosis, Portal hypertension, Splenic vein thrombosis
Genetic	Aicardi Goutieres syndrome, Alpha-mannosidase deficiency, Apolipoprotein C-II deficiency, Chanarin-Dorfman disease, Chediak-Higashi disease, Cholesterol ester storage disease, Familial alphalipoprotein deficiency, Familial histiocytic reticulosis, Familial hypertriglyceridaemia, Farber lipogranulomatosis, Fucosidosis, Fumarate hydratase deficiency, Galactose epimerase deficiency, Galactose-1-phosphate uridyltransferase deficiency, Gamma heavy chain disease, Gangliosidosis GM1, type 1, Gangliosidosis GM1, type 3, GM2 gangliosidosis, Gaucher's disease, Glucose phosphate isomerase deficiency, Glycogen storage disease, Haemochromatosis, Hurler syndrome, Hurler-Scheie syndrome, Hyperlipidemia, Iduronate-2-sulfatase deficiency, Kartagener syndrome, Langerhans cell histiocytosis , Lecithin cholesterol acyltransferase deficiency, Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, McLeod syndrome, Mevalonate kinase deficiency, Mu chain disease, Mucolipidosis II alpha/beta, Mucopolysaccharidosis VI, Mucopolysaccharidosis VII, Nakajo-Nishimura syndrome, Niemann-Pick disease, Prolidase deficiency, Salla disease, Sandhoff disease, Sanfilippo disease, Sea blue histiocytosis, Sialidosis , Sphingomyelinase deficiency, Tyrosinaemia type 1, Zimmermann-Laband syndrome
Hematologic	Acute and chronic hemolytic anemias, all etiologies, Autoimmune hemolytic anemia, Congenital dyserythropoietic anaemia type 1, Congenital erythropoeitic porphyria, Coproporphyria, hereditary, Eosinophillic granuloma, Essential thrombocythemia, Extramedullary haemopoiesis, Haemoglobin C disease, Haemoglobin E disease, Haemoglobin SC disease, Haemolytic disease of the newborn, Hemolytic anemia, Hemophagocytic lymphohistiocytosis, Hereditary spherocytosis, Histiocytosis X, Hypereosinophilic syndrome, Iron deficiency anemia, Letterer-Siwe disease, Mastocytosis, Multiple myeloma, Myelofibrosis, Myeloid leukemia, Myeloid metaplasia, Myeloproliferative syndrome, Osteomyelosclerosis, Paroxysmal nocturnal hemoglobinuria, Polycythemia vera, Primary autoimmune haemolytic anaemia, Primary thrombocythemia, acquired, Rosai-Dorfman disease, Sickle cell crisis, Sickle cell disease, Thalassemia major, Waldenström's macroglobulinemia
Iatrogenic	No underlying causes
Infectious Disease	Acanthocheilonemiasis, AIDS, Babesiosis, Bartonellosis, Borreliosis, Cat-Scratch disease, Coronavirus, Corynebacterium diphtheriae, Cytomegalovirus, Dengue, E.coli, Ehrlichiosis, Group B streptococcal infection, Hepatic Echinococcosis, Hepatitis, Histoplasmosis, Infectious mononucleosis, Kala-Azar, Leishmaniasis, Leptospirosis, Lyme disease, Malaria, Mycobacterium avium complex, Paragonimiasis, Psittacosis, Q fever, Relapsing fever, Rickettsiae, RMSF, Rubella, Salmonella, Schistosomiasis, Septicemia, Sleeping sickness, Splenic abscess, Syphilis, Toxocariasis, Toxoplasma, Trench fever, Tropical splenomegaly syndrome, Trypanosomiasis, Tuberculosis, Tularemia, Visceral larva migrans, Weil syndrome, Whipple disease
Musculoskeletal/Orthopedic	Osteopetrosis
Neurologic	No underlying causes
Nutritional/Metabolic	Nutritional anemias, Vitamin B12 deficiency
Obstetric/Gynecologic	No underlying causes
Oncologic	Acute and chronic leukemias, Adult T-cell leukemia, Angioimmunoblastic lymphadenopathy with dysproteinaemia, Angiosarcoma, Autoimmune lymphoproliferative syndrome, Bone marrow infiltration, Castleman's disease, Chronic eosinophilic leukaemia, Chronic lymphocytic leukaemia, Chronic myeloid leukaemia, Fibroma, Geleophysic dysplasia, Hairy cell leukaemia, Hamartomas, Hepatosplenic T-cell lymphoma,Hodgkin lymphoma, Lymphangiomas, Lymphoid leukemia, Lympho-reticulosarcoma, Mantle cell lymphoma, Melanoma, Metastatic solid tumors, Monocytic leukemia, Non-Hodgkin's lymphoma, Primary splenic tumors, Splenic hamartoma, Splenic hemangioma
Ophthalmologic	No underlying causes
Overdose/Toxicity	No underlying causes
Psychiatric	No underlying causes
Pulmonary	No underlying causes
Renal/Electrolyte	Nephrotic syndrome,
Rheumatology/Immunology/Allergy	Amyloidosis, Collagen vascular diseases, Common variable hypogammaglobulinaemia, Felty's syndrome, Immune hemolytic anemias, Juvenile chronic arthritis, Macrophage activation syndrome, Mixed essential cryoglobulinaemia, Primary biliary cirrhosis, Sarcoidosis, Serum sickness, Still disease, adult-onset, Still disease, juvenile-onset, Systemic lupus erythematosus
Sexual	No underlying causes
Trauma	Trauma
Urologic	No underlying causes
Miscellaneous	Idiopathic splenomegaly, Splenic artery aneurysm, Splenic cyst

Causes in Alphabetical Order

The unnamed parameter 2= is no longer supported. Please see the documentation for {{columns-list}}.

3