Abstract
Angioimmunoblastic lymphadenopathy (AILD) is a recently invidualized atypical lymphoid disease [5, 9, 14]. It is characterized by the presence of peripheral lymph node enlargement, hepatosplenomegaly, cutaneous rash, and constitutional symptoms.
Keywords
- Hemolytic Anemia
- Infectious Mononucleosis
- Nodal Architecture
- Angioimmunoblastic Lymphadenopathy
- Bone Marrow Biopsy Specimen
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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Flandrin, G. (1978). Angioimmunoblastic Lymphadenopathy: Clinical, Biologic, and Follow-up Study of 14 Cases. In: Mathé, G., Seligmann, M., Tubiana, M. (eds) Lymphoid Neoplasias I. Recent Results in Cancer Research, vol 64. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-81246-0_29
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DOI: https://doi.org/10.1007/978-3-642-81246-0_29
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