“…Moreover, the biological pathways involved in hematological malignancies and UC are interlinked, with several mediators of inflammation and cellular populations with an altered response profile being shared among these entities [8]. Indeed, tumor necrosis factor-alpha (TNF-α), nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB), interleukins (IL-1, -5, -6, and -8), angiogenesis factors (i.e., vascular endothelial growth factor (VEGF)), irregular plasmatoid cells inducing pronounced TNF-α and reduced interferon-gamma production, and eosinophils are key-components of the pathogenesis of MM, MDS, SM, and UC [3,[7][8][9][10][11][12]. Further details pertaining to each case are also presented below.…”