M. Fracchia et al., MINIMAL CHANGE NEPHROPATHY PRESENTING IN A PATIENT WITH PRIMARY SCLEROSING CHOLANGITIS, The Italian Journal of Gastroenterology, 29(3), 1997, pp. 267-269
The association of primary sclerosing cholangitis and renal disease is
not frequent, and is limited to a few reported cases of immune comple
x glomerulonephritis. We report the case of a 34-year-old patient with
sclerosing cholangitis diagnosed 5 years earlier with well preserved
liver function and no clinical manifestations of cholestasis, who deve
loped minimal change nephropathy. During the nephrotic phase of the di
sease, the peripheral blood lymphocyte count was normal, with a relati
ve increase in percent CD4+ and an increase in the CD4+:CD8+ ratio. CD
4+ cells showed immunoactivation. The HLA-DR expression on T-cells was
59%, and 16.5% of CD3+ cells were CD25+. A course of prednisone thera
py induced long-lasting remission of the nephrotic syndrome. Periphera
l blood lymphocyte count and subtyping were normal 7 months after pred
nisone withdrawal. We conclude that primary sclerosing cholangitis can
be associated with minimal change nephropathy; underlying cell-mediat
ed immunity may be the common pathogenic mechanism.