HIGHLIGHTS
- who: Report and collaborators from the (UNIVERSITY) have published the research: Review began 12/19/2022 Review ended 01/05/2023 Published 01/07/2023 u00a9 Copyright, in the Journal: (JOURNAL) of January/07,/2023
- what: Although progression to systemic disease is rare, it can occur, which further highlights the importance of a complete diagnostic assessment given the worse prognosis of systemic forms (as was done in this case).
SUMMARY
Amyloidosis is a rare clinical entity characterized by the deposition of amyloid fibrils and insoluble protein polymers in organs or tissues . . .
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