Dm. Menke et al., BONE-MARROW ASPIRATE IMMUNOFLUORESCENT AND BONE-MARROW BIOPSY IMMUNOPEROXIDASE STAINING OF PLASMA-CELLS IN HISTOLOGICALLY OCCULT PLASMA-CELL PROLIFERATIVE MARROW DISORDERS, Archives of pathology and laboratory medicine, 118(8), 1994, pp. 811-814
Citations number
15
Categorie Soggetti
Pathology,"Medical Laboratory Technology","Medicine, Research & Experimental
Immunofluorescent staining (immunofluorescence bone marrow aspirate) a
nd immunoperoxidase staining (immunoperoxidase bone marrow biopsy) wer
e compared in 26 patients with plasma cell dyscrasia and less than 10%
marrow plasma cells. Their clinical diagnoses included monoclonal gam
mopathy of undetermined significance (13 patients), treated multiple m
yeloma (four patients), multiple myeloma with less than 10% marrow pla
sma cells (two patients), primary systemic amyloidosis (two patients),
monoclonal gammopathy of undetermined significance with neuropathy (t
wo patients), angiofollicular lymph node hyperplasia (two patients, al
l with the POEMS [polyneuropathy, organomegaly, endocrinopathy, monocl
onal protein, and skin changes] syndrome), and primary (amyloidosis) a
myloid neuropathy (one patient). The percentage of plasma cells was gr
eater than 5% in 23% of patients and less than or equal to 5% in 77% o
f patients. With immunofluorescence bone marrow aspirate and immunoper
oxidase bone marrow biopsy, light-chain restriction was demonstrated i
n 84% of all cases and accurately determined in 96% of all cases as sh
own by serum and urine paraprotein analysis or tissue amyloid typing.
Monoclonal populations of plasma cells can be readily identified with
immunofluorescence bone marrow aspirate and immunoperoxidase bone marr
ow biopsy in most patients with paraproteins and marrow plasmacytoses
not diagnostic of multiple myeloma.