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Washington University Experience | MISCELLANEOUS | Familial erythrophagic lymphohistiocytosis | 3F7 HLH, Perforin1 mutation (Case 3) GFAP 3

3F7 HLH, Perforin1 mutation (Case 3) GFAP 3
There is substantial astrocytosis immediately adjacent to the vessels. This would not be the appearance of thte histopathology of NMO (GFAP IHC)



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