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**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.Major Scope
- Sarcomas
- Hematology
- Paediatric Cancers
- Radiation Oncology
- Endoscopy Methods
- Surgical Oncology
- Thoracic Oncology
- Palliative Care
Abstract
Citation: Clin Oncol. 2016;1(1):1007.DOI: 10.25107/2474-1663.1007
Aggressive T-cell Large Granular Lymphocytic Leukemia Presenting as an EBV Negative Post-Transplant Lymphoproliferative Disorder
Leeborg N, Loriaux M and Huang JZ
Department of Pathology and Laboratory Medicine, Oregon Health & Science University, Portland, OR, USA
A 33 year-old man, a renal transplant recipient, developed an aggressive T-cell large granular lymphocytic leukemia (LGL) that presented as a soft-tissue lesion, mimicking an abscess. The tumor cells showed cytological features of large granular lymphocytes, immunophenotypically characterized as mature T-cells expressing CD2, CD5, CD4, CD56, and TIA-1. About 80% of tumor cells were positive for Ki-67 and p53. Cytogenetic analysis demonstrated trisomy 8, trisomy 15, and trisomy 21. There was no evidence of Epstein-Barr virus infection. The patient died 14 days after diagnosis with multiple organ failure and extensive bone marrow and visceral involvement. Department of Clinical Pathology, William Beaumont Hospital, Royal Oak, MI, USA and Department of Pathology and Laboratory Medicine, Oakland University William Beaumont School of Medicine, Rochester, MI, USA
*Correspondance to: James Z Huang
PDF Full Text Case Report | Open Access
Abstract:
A 33 year-old man, a renal transplant recipient, developed an aggressive T-cell large granular lymphocytic leukemia (LGL) that presented as a soft-tissue lesion, mimicking an abscess. The tumor cells showed cytological features of large granular lymphocytes, immunophenotypically characterized as mature T-cells expressing CD2, CD5, CD4, CD56, and TIA-1. About 80% of tumor cells were positive for Ki-67 and p53. Cytogenetic analysis demonstrated trisomy 8, trisomy 15, and trisomy 21. There was no evidence of Epstein-Barr virus infection. The patient died 14 days after diagnosis with multiple organ failure and extensive bone marrow and visceral involvement.
Keywords:
T-cell large granular lymphocytic leukemia; Post-transplant lymphoproliferative disorder
Cite the Article:
Leeborg N, Loriaux M, Huang JZ. Aggressive T-cell Large Granular Lymphocytic Leukemia Presenting as an EBV Negative Post-Transplant Lymphoproliferative Disorder. Clin Oncol. 2016; 1: 1007.