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CASE REPORT
Year : 2017  |  Volume : 6  |  Issue : 2  |  Page : 427-430

Peripheral T-cell lymphoma, not otherwise specified


1 Department of Psychiatry, All Institute of Medical Sciences, Patna, Bihar, India
2 Department of Internal Medicine, Forest Glen Medical Center, Silver Spring Maryland, MD, USA
3 Department of Internal Medicine, Royal College of Surgeons in Ireland and Medical University of , Southern Governorate, Bahrain
4 Department of Forensic Medicine, Gandaki Medical College, Pokhara, Nepal

Correspondence Address:
Dr. Kunal Kishor Jha
All India Institute of Medical Sciences, Patna, Bihar
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jfmpc.jfmpc_323_16

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The peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS) belongs to a heterogeneous class of aggressive neoplasms. Although several morphologic subtypes of this tumor have been described, no particular genetic, immunological, or distinct clinical features define this disease. Patients can experience night sweats, fever, lymphadenopathy, weight loss, splenomegaly, and/or skin changes. Common laboratory tests reveal that patients have anemia, thrombocytosis, lymphocytosis, eosinophilia, hypergammaglobulinemia, or increased lactate dehydrogenase. In this case study, a patient presented with massive lymphadenopathy and right lower limb swelling, which he developed over 6 weeks. A tissue biopsy and supporting investigations confirmed the diagnosis of PTCL, NOS.


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