KEY FACTS

Imaging

  • 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

Top Differential Diagnoses

  • Splenic infection and abscess

    • Pyogenic/fungal abscess or parasitic echinococcal cyst

  • Splenic metastases and lymphoma

  • Benign primary splenic tumors

  • Intrasplenic pseudocyst

Pathology

  • 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

Clinical Issues

  • 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)

Axial CECT shows a water density mass with a calcified wall
within the spleen. Note the absence of any enhancing or soft tissue components within this splenic cyst.

Postsplenectomy specimen in the same patient shows the calcified, fibrous wall of the cyst. This was an acquired cyst, probably as a result of prior trauma or infarction.

Coronal CECT in a young woman demonstrates a large, simple-appearing splenic cyst
. The patient was symptomatic with pain and early satiety and consequently underwent surgical cyst deroofing.

Axial CECT demonstrates a large, nonenhancing, multiseptated splenic cyst
replacing most of the spleen. Only a posterior sliver of normal spleen remains
.

IMAGING

General Features

  • 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

Radiographic Findings

  • Curvilinear wall calcification in left upper quadrant

CT Findings

  • 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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