Splenomegaly
Splenomegaly
Updated: 07/13/2020
© Jun Wang,
MD, PhD
General features
- Enlarged spleen >400 g
- Massive if > 1000 g
- Various etiology, usually associated with splenic hyperfunction
Etiology
- Part of systemic presentation of inflammation: Such as in subacute bacterial endocarditis or infectious mononucleosis
- Local inflammation: Sarcoidosis, abscess, etc
- RBC destruction: Hereditary spherocytosis, thalassemia
- Congestive: Portal hypertension
- Ectopic hematopoiesis: Myeloproliferative neoplasm, etc
- Neoplastic: Lymphomas, metastatic malignancy, etc
Clinical presentations
- Various
Key pathogenesis
- Splenic hyperfunction
Key Laboratory findings
- Nonspecific
- Anemia, leukopenia, or thrombocytopenia
- Less mature white cells, nucleated red cells, teardrop-shaped red cells, etc
Diagnostic approaches to
identify etiology
- History
- CBC and peripheral blood morphology
- Bone marrow biopsy if hematopoietic disorder suspicious
- Flow cytometry if lymphocyte predominance
- Liver functions
- Image studies
- Molecular studies
Back to contents
Comments
Post a Comment