Progression of dialysis-related amyloidoma towards pathologic fracture.

Skeletal Radiol

School of Medicine, University of California, San Francisco, 400 Parnassus Ave, A-367, San Francisco, CA, 94143, USA.

Published: February 2019


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Article Abstract

Amyloidosis is the extracellular deposition of amyloid protein fibrils, and this condition may be hereditary or acquired. Patients undergoing long-term hemodialysis are particularly at risk for developing acquired amyloidosis. A rare form of amyloidosis is an amyloidoma or amyloid tumor, which occurs when amyloid focally deposits in a section of the musculoskeletal system, most commonly in the osteoarticular system. Here, we present a case of a hemodialysis-related amyloidoma of the left femoral neck in an 80-year-old woman with end-stage renal disease on hemodialysis for 8 years. The purpose of this report is to provide an account of the unique clinical, imaging, and histopathologic manifestation of a dialysis-related amyloidoma that progressively enlarges over a 2-year period. This report also highlights some prophylactic measures that may reduce the risk of developing an associated pathologic fracture.

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http://dx.doi.org/10.1007/s00256-018-3009-2DOI Listing

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Progression of dialysis-related amyloidoma towards pathologic fracture.

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School of Medicine, University of California, San Francisco, 400 Parnassus Ave, A-367, San Francisco, CA, 94143, USA.

Amyloidosis is the extracellular deposition of amyloid protein fibrils, and this condition may be hereditary or acquired. Patients undergoing long-term hemodialysis are particularly at risk for developing acquired amyloidosis. A rare form of amyloidosis is an amyloidoma or amyloid tumor, which occurs when amyloid focally deposits in a section of the musculoskeletal system, most commonly in the osteoarticular system.

View Article and Find Full Text PDF