Splenomegaly causes: Difference between revisions
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| '''Genetic''' | | '''Genetic''' | ||
|bgcolor="Beige"| [[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]], [[Gangliosidosis GM3]], [[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]] | |bgcolor="Beige"| [[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]], [[Gangliosidosis GM3]], [[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]] | ||
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Revision as of 16:09, 31 October 2016
Template:Splenomegaly Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Causes
Causes by Organ System
Causes in Alphabetical Order[1] [2]
The unnamed parameter 2= is no longer supported. Please see the documentation for {{columns-list}}.
3Less common causes [3]
- Amyloidosis
- Babesiosis
- Gaucher's disease
- Histoplasmosis
- Kala-azar
- Rickets
- Schistosomiasis
- Syphilis
- Toxoplasmosis
- Typhoid fever
Causes by Organ System
Splenomegaly grouped on the basis of the pathogenic mechanism
Causes of Massive Splenomegaly (>1000gms)
- 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
References
- ↑ Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:77 ISBN 1591032016
- ↑ Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:68 ISBN 140510368X
- ↑ Kahan, Scott, Smith, Ellen G. In a page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:157