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Washington University Experience | MISCELLANEOUS | Familial erythrophagic lymphohistiocytosis | 3F5 HLH, Perforin1 mutation (Case 3) CD3 20X 2

3F5 HLH, Perforin1 mutation (Case 3) CD3 20X 2
There is a rich T cell infiltrate (CD3 IHC)



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