Difference between revisions of "Reactive follicular hyperplasia"
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*[[Hodgkin lymphoma]] - with rare Reed-Sternberg cells. | *[[Hodgkin lymphoma]] - with rare Reed-Sternberg cells. | ||
*Non-Hodgkin [[lymphoma]]. | *Non-Hodgkin [[lymphoma]]s. | ||
**[[Follicular lymphoma]]. | |||
**T-cell/histiocyte-rich large B cell lymphoma. | **T-cell/histiocyte-rich large B cell lymphoma. | ||
**Others. | |||
==IHC== | ==IHC== | ||
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===Images=== | ===Images=== | ||
<gallery>Image:Follicular lymphoma - control bcl2 -- low mag.jpg|BCL2 negative immunostaining in the germinal centers of reactive follicular hyperplasia. [[BCL2|BCL2 immunostain]]. | |||
</gallery> | |||
==See also== | ==See also== |
Latest revision as of 15:25, 16 February 2021
Reactive follicular hyperplasia is a benign lymph node change.
General
- Many causes - including: bacteria, viruses, chemicals, drugs, allergens.
- In only approximately 10% can definitive cause be identified.[1]
Microscopic
Features:[2]
- Enlarged follicles, follicle size variation - key feature with:
- Large germinal centers (pale on H&E).
- Mitoses common.
- Variable lymphocyte morphology.
- Tingible-body macrophage (large, pale cells with junk in the cytoplasm).
- Germinal centers (GCs) have a crisp/sharp edge.
- Normal dark/light variation of GCs; superficial aspect light, deeper aspect darker.
- Rim of small (inactive) lymphocytes.
- Large germinal centers (pale on H&E).
DDx:
- Hodgkin lymphoma - with rare Reed-Sternberg cells.
- Non-Hodgkin lymphomas.
- Follicular lymphoma.
- T-cell/histiocyte-rich large B cell lymphoma.
- Others.
IHC
Screening panel:
Others:
- BCL2 -ve.
- Germinal centers negative.
Images
BCL2 negative immunostaining in the germinal centers of reactive follicular hyperplasia. BCL2 immunostain.
See also
References
- ↑ Ioachim, Harry L; Medeiros, L. Jeffrey (2008). Ioachim's Lymph Node Pathology (4th ed.). Lippincott Williams & Wilkins. pp. 174. ISBN 978-0781775960.
- ↑ Ioachim, Harry L; Medeiros, L. Jeffrey (2008). Ioachim's Lymph Node Pathology (4th ed.). Lippincott Williams & Wilkins. pp. 179. ISBN 978-0781775960.