Angioimmunoblastic T-cell lymphoma overview: Difference between revisions
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Revision as of 12:21, 17 August 2015
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Angioimmunoblastic T-cell lymphoma Microchapters |
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Differentiating Angioimmunoblastic T-cell lymphoma from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Angioimmunoblastic T-cell lymphoma overview On the Web |
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American Roentgen Ray Society Images of Angioimmunoblastic T-cell lymphoma overview |
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Directions to Hospitals Treating Angioimmunoblastic T-cell lymphoma |
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Risk calculators and risk factors for Angioimmunoblastic T-cell lymphoma overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [3]
Overview
Angioimmunoblastic T-cell lymphoma (AILT) is a mature T-cell lymphoma characterized by a polymorphous lymph node infiltrate showing a marked increase in follicular dendritic cells (FDCs) and high endothelial venules (HEVs) and systemic involvement.[1] It is also known as immunoblastic lymphadenopathy (Lukes-Collins Classification) and AILD-type (lymphogranulomatosis X) T-cell lymphoma (Kiel Classification)[1].
References