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See Latest ArticlesHereditary gelsolin amyloidosis mimicking Sjögren’s syndrome
Clinical Rheumatology, 08/25/09
Juusela P et al. – The authors present a case of sicca syndrome, originally diagnosed as primary Sjögren's syndrome (SS) but later found to represent an initial disease manifestation of AGel amyloidosis, not recognised earlier. This case emphasises both the importance of specific amyloid stainings and comprehensive salivary gland histopathology as well as family history in SS differential diagnostics.
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