N. Yokota et al., Reversible nephrotic syndrome in a patient with amyloid A amyloidosis of the kidney following methicillin-resistant Staphylococcus aureus infection, NEPHRON, 87(2), 2001, pp. 177-181
A corn mon form of methicillin-resistant Staphylococcus aureus (MRSA) assoc
iated glomerulonephritis is either an endocapillary proliferative glomerulo
nephritis or a crescentic glomerulonephritis. This report describes the dev
elopment of reversible nephrotic syndrome following MRSA infection in a pat
ient with amyloid A amyloidosis. The patient had been diagnosed as having r
heumatoid arthritis for 50 years. Suppurative arthritis due to MRSA became
complicated 2 years prior to admission to our hospital. In the meantime, a
nonnephrotic-range proteinuria developed. Two weeks before admission,nephro
tic syndrome developed. The serum creatinine level remained unchanged throu
ghout the course, but common features characteristic of MRSA-associated glo
merulonephritis were observed in this patient, such as elevated serum IgG a
nd IgA levels. A renal biopsy specimen showed glomerular amyloid A amyloido
sis of a nodular type, infiltrated mononuclear cells in the mesangium, depo
sition of IgG, IgA, and C3, and swelling of glomerular endothelial cells. T
here were no crescentic glomeruli. Following surgical eradication of the MR
SA focus in the right knee joint, nephrotic syndrome disappeared. Hence, it
was highly possible that MRSA infection induced a reversible nephrotic syn
drome by causing reversible injuries to glomerular endothelial cells. The d
escription of this case serves to illustrate the range of MRSA infections t
hat may cause various forms of glomerulonephritides. Copyright (C) 2001 S.
Karger AG, Basel.