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TCL-1-positive hematogones in a patient with T-cell prolymphocytic leukemia after therapy.

Abstract
T-prolymphocytic leukemia (T-PLL) is a rare mature T-cell neoplasm characterized by proliferation of prolymphocytes. Most cases involve the T-cell leukemia-1 (TCL1) gene at 14q11.2 resulting in overexpression of TCL-1, which is helpful for distinguishing T-PLL from other T-cell neoplasms. We report a patient with T-PLL whose leukemic cells were positive for TCL-1 by immunohistochemistry but with a normal karyotype. The patient had anti-CD52 antibody therapy for 12 weeks. In a follow-up bone marrow biopsy specimen, numerous TCL-1-positive cells were present, which raised the differential diagnosis of residual T-PLL. However, further immunophenotypic studies confirmed that these cells were hematogones. Therefore a diagnosis of recovering bone marrow was established. The patient underwent stem cell transplant and is now in complete remission. This case demonstrates that hematogones can express TCL-1, and this knowledge is very important for the differential diagnosis in the follow-up marrow of T-PLL patients.
AuthorsZhihong Hu, Shaoying Li, L Jeffrey Medeiros, Tsieh Sun
JournalHuman pathology (Hum Pathol) Vol. 65 Pg. 175-179 (07 2017) ISSN: 1532-8392 [Electronic] United States
PMID28232160 (Publication Type: Case Reports, Journal Article)
CopyrightCopyright © 2017 Elsevier Inc. All rights reserved.
Chemical References
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Biomarkers, Tumor
  • Proto-Oncogene Proteins
  • TCL1A protein, human
  • Alemtuzumab
Topics
  • Alemtuzumab
  • Antibodies, Monoclonal, Humanized (therapeutic use)
  • Antineoplastic Agents (therapeutic use)
  • Biomarkers, Tumor (genetics, metabolism)
  • Biopsy
  • Bone Marrow Cells (drug effects, metabolism)
  • Bone Marrow Examination
  • Diagnosis, Differential
  • Humans
  • Immunohistochemistry
  • Karyotyping
  • Leukemia, Prolymphocytic, T-Cell (genetics, metabolism, therapy)
  • Male
  • Middle Aged
  • Predictive Value of Tests
  • Proto-Oncogene Proteins (genetics, metabolism)
  • Remission Induction
  • Stem Cell Transplantation
  • Treatment Outcome

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