Macroglossia, the first manifestation of systemic amyloidosis associated with multiple myeloma: Case report

2018 ◽  
Vol 119 (6) ◽  
pp. 514-517 ◽  
Author(s):  
A. Maturana-Ramírez ◽  
A.V. Ortega ◽  
F.C. Labbé ◽  
Ê. de Moraes ◽  
J.P. Aitken-Saavedra
2005 ◽  
Vol 84 (6) ◽  
pp. 358-361 ◽  
Author(s):  
Sandra Doria Xavier ◽  
Ivo Bussoloti Filho ◽  
Helena Müller

Amyloidosis is characterized by an abnormal extracellular deposition of amyloid in different tissues and organs, where it usually causes some type of dysfunction. Its cause is unknown. The two main forms of amyloidosis are systemic and localized; the latter is rare. No satisfactory treatment for systemic amyloidosis has been discovered, and mean survival is poor, ranging from 5 to 15 months depending on the presence or absence of multiple myeloma. We report a case of primary systemic amyloidosis in a 71-year-old man. The diagnosis of amyloidosis was established by tongue biopsy, and its systemic nature was identified by analysis of aspirated abdominal fat. At the 1-year follow-up, the patient's clinical condition had not changed, and he was thereafter lost to follow-up.


2019 ◽  
Author(s):  
Eithar Deyab ◽  
Muhammad Esakji ◽  
Neil Rabin ◽  
Ravi Menon ◽  
Girish Rayanagoudar

Author(s):  
Roberto Mina ◽  
Francesca Bonello ◽  
Francesca Gay ◽  
Elena Zamagni ◽  
Mario Boccadoro

2005 ◽  
Vol 130 (6) ◽  
pp. 277-277
Author(s):  
F Zettl ◽  
W Jung ◽  
R Schroers
Keyword(s):  

Author(s):  
KAREN LOUREIRO WEIGERT ◽  
MARCELO EDUARDO ZANELLA CAPRA ◽  
DANIEL SCHEBELA MAZZOLENI ◽  
FABIOLA RAMPANELLI FRANCO
Keyword(s):  

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