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Spectrum of appearances on CT
Solitary, well-defined, water density, unilocular cystic lesion
Thin wall with sharp interface to normal splenic tissue
No peripheral/intracystic enhancement or solid component
Some cysts can have septations, trabeculations, thick wall, internal necrotic debris, or calcification
May have attenuation greater than simple fluid (due to hemorrhage or protein)
Thin eggshell calcification or thick, irregular peripheral calcification
Congenital and acquired cysts may be indistinguishable
Congenital cysts more likely simple in appearance
Acquired cysts often complex with calcification
Splenic infection and abscess
Pyogenic/fungal abscess or parasitic echinococcal cyst
Splenic metastases and lymphoma
Benign primary splenic tumors
Intrasplenic pseudocyst
Congenital epidermoid ("true" cyst)
May be due to intrasplenic sequestration of peritoneal mesothelial cells during embryologic development
Acquired cysts (secondary/"false" cysts or pseudocysts)
Due to prior trauma, hematoma, infarction, or infection
Majority of splenic cysts in North America due to prior trauma
Arise due to liquefactive necrosis and cystic change
Most cysts are discovered incidentally on imaging
Small and asymptomatic: No treatment
Symptomatic cysts usually treated, with options including percutaneous aspiration/drainage, cyst decapsulation or unroofing, and partial/complete splenectomy
Splenectomy for symptomatic large cysts (> 5 cm)
Best diagnostic clue
Sharply defined, spherical cystic lesion of water density
Key concepts
Classification
Congenital epidermoid cysts (primary or "true" cyst)
Demonstrate inner cellular endothelial lining
Account for 10-25% of all splenic cysts
Acquired cysts (secondary or "false" cysts)
No inner cellular lining but have fibrous wall
Account for 80% of splenic cysts
Due to prior trauma, hematoma, or infarction
Development of cyst due to liquefactive necrosis
Curvilinear wall calcification in left upper quadrant
Spectrum of appearances
Solitary, well-defined, water density unilocular cyst
Thin wall with sharp interface to normal splenic tissue
No peripheral or intracystic enhancement; no solid, nodular soft tissue component
Always intraparenchymal (no exophytic component)
Some cysts can have septations, trabeculations, thick wall, and internal necrotic debris
May have attenuation greater than simple fluid (due to hemorrhage or protein)
Cysts may have thin eggshell calcification or thick, irregular peripheral calcification
Congenital and acquired cysts may be indistinguishable
Congenital cysts more likely to be simple in appearance
Acquired cysts more likely complex with calcification
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