Eh. Strom et al., IMMUNOTACTOID-LIKE GLOMERULOPATHY WITH MASSIVE FIBRILLARY DEPOSITS INLIVER AND BONE-MARROW IN MONOCLONAL GAMMOPATHY, American journal of nephrology, 16(6), 1996, pp. 523-528
At autopsy, massive nonamyloid fibrillar deposits, immunoreactive to I
gG and kappa light chain, were found in glomeruli, liver, and bone mar
row of a 72-year-old woman. The patient suffered from severe nephrotic
syndrome, hepatomegaly and cholestasis, normochromic anemia, and IgG
kappa monoclonal gammopathy. Fibrillary glomerulopathies, most often d
enoted as fibrillary glomerulonephritis or immunotactoid glomerulopath
y, are generally considered to have deposits restricted to the glomeru
li. However, this study indicates that fibrillary deposits may be a sy
stemic manifestation of fibrillary glomerulonephritis or immunotactoid
glomerulopathy, at least when the patient is suffering from a monoclo
nal gammopathy.