38 yrs old male with hyperglobulinemia (esp. IgM), hepatosplenomegaly underwent threpine biopsy.
HISTO: The prominenet infiltration of macrofages, focal serous degeneration, architectural abnormalities, erythroid hyperplasia. Definite features of hemophagocytosis are absent. The single mixed B/T (reactive) peritrabecullar follicle is present. Intersticial lymhoid population: CD3+ > CD20+ (reactive). CLIN DIAGNOSIS: Waldenstrom disease (LPL)??? IH: Nothing special. The single CD117+ mastocytes. Ig kappa/lambda monotypic. PAS staining (not standard in our BMs) is in progress. PROPOSAL: Reactive changes: the prominent macrophageal reaction in BM: hemophagocytosis? Virus induced? Etc.? Thank you fo being 2gether.
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Last modified: 2007-11-12 09:18:48