Abstract
Castleman disease (CD) is a benign angiofollicular lymph node hyperplasia usually found in the mediastinum, but the pelvis is rarely affected. Descriptions of the pelvic CD mainly involve computed tomography (CT) features and focal well-defined masses, while descriptions based on magnetic resonance imaging (MRI) patterns and infiltrating masses are rare.Through a case of a pelvic CD, unusual in its radiological appearance, the authors analyse imaging features as suggested by CT and MRI in order to improve the recognition of this rare disease.
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