Peripheral Lymphocytosis in Angioimmunoblastic T-cell Lymphoma

Angioimmunoblastic T-cell lymphoma (AITL) is an aggressive and unique type of T-cell lymphoma. Patients typically present with constitutional B symptoms, generalized lymphadenopathy, hepatosplenomegaly, cytopenias, and rash. We report a 63-year-old male who presented with fever, generalized lymphade...

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Bibliographic Details
Published in:International Journal of Advanced Medical and Health Research
Main Authors: C. Selvapriya, Nidhya Ganesan, Sakthisankari Shanmugasundaram, Narmadha Rathinasamy, Prasanna Nedungadi Kumar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-12-01
Subjects:
gammopathy
non-hodgkin’s lymphoma
plasma cell dyscrasia
Online Access:https://journals.lww.com/10.4103/ijamr.ijamr_6_24
Description
Summary:Angioimmunoblastic T-cell lymphoma (AITL) is an aggressive and unique type of T-cell lymphoma. Patients typically present with constitutional B symptoms, generalized lymphadenopathy, hepatosplenomegaly, cytopenias, and rash. We report a 63-year-old male who presented with fever, generalized lymphadenopathy, and features of plasma cell dyscrasia. Our report emphasizes the complexity of the presentation of AITL and aims to sensitize physicians for early diagnosis and an integrated treatment approach.
ISSN:2349-4220
2350-0298

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