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Morphology, immunophenotype, and suggested diagnostic criteria of TCL1 family-negative T-prolymphocytic leukemia.

Hong FangSa A WangHannah C BeirdZhenya TangM James YouShaoying LiJie XuShimin HuC Cameron YinSiba El HusseinPei LinFatima Zahra JelloulFrancisco VegaL Jeffrey MedeirosWei Wang
Published in: American journal of clinical pathology (2024)
TCL1 family-negative T-PLL cases have morphologic and immunophenotypic features that are similar to prototypic T-PLL. They are characterized by neoplastic proliferation of small to medium-sized mature T cells with CD4-positive T-cell receptor αβ phenotype. Tumor cells frequently maintain pan-T antigen expression. Recognizing these morphologic and immunophenotypic features will aid in accurately diagnosing this rare subset of T-PLL.
Keyphrases
  • poor prognosis
  • acute myeloid leukemia
  • signaling pathway
  • bone marrow
  • long non coding rna
  • nk cells