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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| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2024-12-01
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| Series: | International Journal of Advanced Medical and Health Research |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/ijamr.ijamr_6_24 |
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| 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. |
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| ISSN: | 2349-4220 2350-0298 |