Related Experiment Video
Updated: Aug 15, 2025

06:33
Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
7.8K
Breast Amyloidosis: A Case Report and Literature Review
Anne-Sofie De Crem1, Koen Van de Vijver2, Pieter De Visschere2
1UGent, BE.
Journal of the Belgian Society of Radiology
|January 2, 2023
Summary
Localized breast amyloidosis, a rare protein buildup disorder, can mimic microcalcifications on mammography. Early diagnosis via biopsy is key for prognosis, especially in patients with systemic lupus erythematosus.
Area of Science:
- Oncology
- Rheumatology
- Pathology
Background:
- Amyloidosis is an uncommon condition involving the extracellular deposition of misfolded proteins.
- Localized breast amyloidosis is a rare manifestation, often presenting subtly on imaging.
- Systemic lupus erythematosus (SLE) is an autoimmune disease that can be associated with various systemic complications.
Purpose of the Study:
- To report a unique case of localized breast amyloidosis in an asymptomatic patient with SLE.
- To highlight the mammographic findings and diagnostic approach for this rare condition.
- To discuss the recommended management and prognosis of localized breast amyloidosis.
Main Methods:
- Case presentation of a 56-year-old woman with asymptomatic localized breast amyloidosis.
- Mammographic evaluation revealing suspicious microcalcifications without a discernible mass.
- Confirmation of amyloidosis through vacuum biopsy with Congo-red staining and polarized light microscopy.
Main Results:
- The case demonstrated localized breast amyloidosis presenting as mammographic microcalcifications.
- Congo-red staining showed characteristic apple-green birefringence under polarized light, confirming amyloid deposition.
- The patient was asymptomatic, and no mass was detected on initial mammography.
Conclusions:
- Localized breast amyloidosis can present as suspicious microcalcifications, mimicking other breast pathologies.
- Vacuum biopsy is crucial for diagnosis, and polarized light microscopy is essential for characteristic findings.
- Further workup to rule out systemic amyloidosis or hematologic malignancy is recommended; prognosis is favorable if negative.

