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Updated: Apr 27, 2026

Flow Cytometry to Estimate Leukemia Stem Cells in Primary Acute Myeloid Leukemia and in Patient-derived-xenografts, at Diagnosis and Follow Up
Published on: March 26, 2018
Adult T-cell leukemia/lymphoma
Robbie L Graham1, Micah Burch1, John R Krause1
1Department of Pathology, Section of Hematopathology (Graham, Krause), and the Department of Hematology/Oncology (Burch), Baylor University Medical Center at Dallas and Baylor Charles A. Sammons Cancer Center, Dallas, Texas.
Adult T-cell leukemia/lymphoma, a rare cancer linked to human T-cell lymphotropic virus type 1 (HTLV-1), presents with diverse clinical features. This case highlights unique aspects of de novo adult T-cell leukemia/lymphoma.
Area of Science:
- Hematology
- Oncology
- Virology
Background:
- Adult T-cell leukemia/lymphoma (ATLL) is a rare lymphoid malignancy.
- It is caused by the human retrovirus, human T-cell lymphotropic virus type 1 (HTLV-1).
- ATLL presents with diverse clinical manifestations and prognoses based on subtype.
Observation:
- This report details a case of de novo ATLL.
- The patient exhibited a proliferation of highly pleomorphic lymphocytes.
- Disease involvement included peripheral blood, bone marrow, lymph nodes, spleen, and extranodal sites.
Findings:
- The case showcases unique clinical, morphologic, and immunophenotypic features.
- Molecular characteristics of this de novo ATLL are discussed.
- The presentation varied from typical aggressive forms.
Implications:
- Understanding unique ATLL presentations is crucial for diagnosis and management.
- This case contributes to the knowledge of HTLV-1-associated malignancies.
- Further research into diverse ATLL subtypes can improve patient outcomes.
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