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http://www.isn-online.org/education/education-topics/pathology-topics/item/962-renal-pathology-case-2#sigProId1e6b866c8f
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67 years old female patient, presented with SOB for 2 months, found to have anemia with renal impairment and nephrotic range proteinuria.
Hala Kfoury Kassouf is Associate Professor of Pathology at the King Saud University Hospital in Saudi Arabia.
I also agree with this suggestion. In fact, the other way round may be more interesting. The juniors should comment on these and finally the case provider should sum up and bring forth important points for the diagnosis. This will generate interest in the junior residents.
Hi! That is quite good case in term of bright illustration of clinical settings and EM-pattern for LCDD. At the same time IF is not representable and doesn't show light chain restriction. I'd prefer to look at PAS stain for complete explanation of clinical data namely nephrotic range proteinuria. I wonder if there is nodular glomerulopathy or secondary segmental glomerulosclerosis. Presented IF and EM both show only tubular changes.
the EM shows tubular electron dense deposits in the subendothelial location. the IF shows linear kappa light chain deposition on tubular epithelium which is negative for lambda, so this a case of monoclonal deposition disease, light chain type...
nice case
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