Splenic amyloidosis

Last revised by Niki Lama on 18 Mar 2025

Splenic amyloidosis is rare as an isolated entity. Most often it is associated with either systemic amyloidosis or hepatic amyloidosis.

In general, splenic involvement in amyloidosis is rather frequent (5-10% of cases 6,7).

Symptoms include abdominal mass and left upper quadrant pain. But there is no corellation with the size of the spleen 8.

Plain radiography is neither sensitive nor specific but may show splenomegaly.

  • splenomegaly

  • calcification is rarely seen 7

  • non-contrast CT shows ill-defined heterogeneous lesions

  • post-contrast CT shows heterogeneous enhancement and hypoperfusion of spleen, which is one of the important indicators of systemic amyloidosis

  • splenomegaly or not

  • T2: affected regions may show decreased signal intensity 1,7

  • on CMR

    - no correlation with the values on T1 NATIVE map

    - really high, diffuse ECV

    - on LGE images the spleen has a specific really high gadolinium uptake ("white spleen") 8

Imaging differential considerations include splenic involvement with:

:

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