Acquired FXIII deficiency and AL amyloidosis: A case of a rare association
Transfus Apher Sci
.
2020 Dec;59(6):102903.
doi: 10.1016/j.transci.2020.102903.
Epub 2020 Aug 15.
Authors
A Ferretti
1
,
E Baldacci
2
,
F Fazio
2
,
R Abbruzzese
2
,
F Barone
2
,
M L De Luca
2
,
M T Petrucci
2
,
A Chistolini
2
,
M G Mazzucconi
2
,
C Santoro
2
Affiliations
1
Hematology, Department of Translational and Precision Medicine, Sapienza University, Policlinico Umberto, Rome, Italy. Electronic address:
[email protected]
.
2
Hematology, Department of Translational and Precision Medicine, Sapienza University, Policlinico Umberto, Rome, Italy.
PMID:
32839100
DOI:
10.1016/j.transci.2020.102903
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Factor XIII Deficiency / diagnosis*
Humans
Immunoglobulin Light-chain Amyloidosis / diagnosis*
Male
Middle Aged