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Submitted by Dr. L. Salinas
Dear colleagues:
I need your opinion on this case: 18 y/o female. Renal
transplant in 1999 (ESRD sec. to reflux nephropathy). Several episodes of
"rejection", with corresponding biopsies (read at another
institution) interpreted as TI rejection, all with abundant plasma cells.
Suspected of polyoma infection, but never demonstrated in the tissues. The
patient was referred to us. Two biopsies at our institution have shown: 1)
massive loss of tubules, 2) an interstitial infiltrate with abundant or
exclusive plasma cells (last biopsy: RB02-169, attached), and 3) advanced
small vessels disease, with tortuosity, thickening, obliteration, and
prominent hyalinization (quite consistent with calcineurin inhibitors
toxicity). The patient has been compliant with treatment. Our stains for CMV,
SV40 and EBV have been repeatedly negative, and the cells are polyclonal. The
first C4d was negative, but the current biopsy shows diffuse prominent
interstitial capillary staining. Could
this case have plasma cell mediated humoral rejection ?
What else ? the clinic and I need some guidance for appropriate
treatment.
Thanks,
Luis
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