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Washington University Experience | MISCELLANEOUS | Familial erythrophagic lymphohistiocytosis | 3C1 HLH, Perforin1 mutation (Case 3) A2 H&E 10X 2
Low magnification image of this H&E stained neurosurgical specimen shows multiple collections of cells suggesting a diagnosis of ADEM, although there is little obvious perivascular myelin pallor. (H&E)
