Presence of fluorescent in situ hybridization abnormalities is associated with plasma cell burden in light chain amyloidosis
Author(s) -
Lindsay Hammons,
Ruta Brazauskas,
Marcelo C. Pasquini,
Mehdi Hamadani,
Parameswaran Hari,
Anita D’Souza
Publication year - 2017
Publication title -
hematology/oncology and stem cell therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 22
eISSN - 1658-3876
pISSN - 2589-0646
DOI - 10.1016/j.hemonc.2017.07.005
Subject(s) - amyloidosis , fluorescence in situ hybridization , medicine , al amyloidosis , amyloid (mycology) , pathology , multiple myeloma , fish <actinopterygii> , stage (stratigraphy) , plasma cell , bone marrow , gastroenterology , immunoglobulin light chain , biology , immunology , antibody , biochemistry , chromosome , gene , paleontology , fishery
To assess abnormalities found on CD138-enriched fluorescent in situ hybridization (FISH) studies on pre-treatment bone marrow in systemic amyloid light-chain amyloidosis (AL) and correlate findings between these abnormalities with organ involvement and 1-year survival.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom