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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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