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Washington University Experience | MISCELLANEOUS | Familial erythrophagic lymphohistiocytosis | 3F8 HLH, Perforin1 mutation (Case 3) SMA 1

3F8 HLH, Perforin1 mutation (Case 3) SMA 1
Although the vessels show significant intramural infiltrate, they fail to show frank vasculitis with wall destruction (Smooth muscle actin, SMA)



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