Difference between revisions of "Primary mediastinal B-cell lymphoma"
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Features:<ref name=pmid19074109 >{{Cite journal | last1 = Johnson | first1 = PW. | last2 = Davies | first2 = AJ. | title = Primary mediastinal B-cell lymphoma. | journal = Hematology Am Soc Hematol Educ Program | volume = | issue = | pages = 349-58 | month = | year = 2008 | doi = 10.1182/asheducation-2008.1.349 | PMID = 19074109 }}</ref><ref name=pmid20207294>{{Cite journal | last1 = Coso | first1 = D. | last2 = Rey | first2 = J. | last3 = Bouabdallah | first3 = R. | title = [Primary mediastinal B-cell lymphoma] | journal = Rev Pneumol Clin | volume = 66 | issue = 1 | pages = 32-5 | month = Feb | year = 2010 | doi = 10.1016/j.pneumo.2009.12.007 | PMID = 20207294 }}</ref> | Features:<ref name=pmid19074109 >{{Cite journal | last1 = Johnson | first1 = PW. | last2 = Davies | first2 = AJ. | title = Primary mediastinal B-cell lymphoma. | journal = Hematology Am Soc Hematol Educ Program | volume = | issue = | pages = 349-58 | month = | year = 2008 | doi = 10.1182/asheducation-2008.1.349 | PMID = 19074109 }}</ref><ref name=pmid20207294>{{Cite journal | last1 = Coso | first1 = D. | last2 = Rey | first2 = J. | last3 = Bouabdallah | first3 = R. | title = [Primary mediastinal B-cell lymphoma] | journal = Rev Pneumol Clin | volume = 66 | issue = 1 | pages = 32-5 | month = Feb | year = 2010 | doi = 10.1016/j.pneumo.2009.12.007 | PMID = 20207294 }}</ref> | ||
*Rare. | *Rare. | ||
*Young adults | *Young adults, more common in females (M:F = 1:2) | ||
*[[Mediastinum]]. | *[[Mediastinum]]. | ||
Line 20: | Line 20: | ||
DDx: | DDx: | ||
*Other types of [[DLBCL]] | *Other types of [[DLBCL]] (radiological assessment is important - PMBCL is centred in the mediastinum) | ||
*B-cell lymphoma with features intermediate between [[DLBCL]] and classical Hodgkins lymphoma | |||
*Poorly differentiated carcinoma. | *Poorly differentiated carcinoma. | ||
==IHC== | |||
*Pan B-cell markers | |||
*CD10 in minority (~20%) | |||
*CD23 and CD30 expression more common (~70% and ~85% respectively) | |||
*EBV negative | |||
===Images=== | ===Images=== | ||
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==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Diagnosis]] | [[Category:Diagnosis]] | ||
[[Category:Lymphoma]] | [[Category:Lymphoma]] |
Revision as of 17:43, 12 May 2018
Primary mediastinal B-cell lymphoma, abbreviated PMBL, is an uncommon form of large B-cell lymphoma.
It is also known as primary mediastinal large B-cell lymphoma.
General
- Rare.
- Young adults, more common in females (M:F = 1:2)
- Mediastinum.
Microscopic
Features:
- Atypical large lymphoid cells - see DLBCL.
- Classically associated with:
- Fibrosis
- Clear cells.
Note:
DDx:
- Other types of DLBCL (radiological assessment is important - PMBCL is centred in the mediastinum)
- B-cell lymphoma with features intermediate between DLBCL and classical Hodgkins lymphoma
- Poorly differentiated carcinoma.
IHC
- Pan B-cell markers
- CD10 in minority (~20%)
- CD23 and CD30 expression more common (~70% and ~85% respectively)
- EBV negative
Images
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MASS, ANTERIOR MEDIASTINAL, CORE BIOPSY: - LARGE B-CELL LYMPHOMA IN A FIBROTIC BACKGROUND WITH NECROSIS, SEE COMMENT COMMENT: Morphology: Tumour cells: size ~2x a mature lymphocyte, a moderate quantity of grey/basophilic cytoplasm, no clear cells are identified. Cells intermixed with tumour: mature lymphocytes, rare eosinophils. Architecture: no gland formation, discohesive, no follicles apparent, extensive fibrosis. Tumour cells: POSITIVE: CD45, CD20, CD10, BCL-6, BCL-2. NEGATIVE: pankeratin, PLAP, CD3, CD30. Ki-67: 50% of large (lymphoid) cells.
See also
References
- ↑ Johnson, PW.; Davies, AJ. (2008). "Primary mediastinal B-cell lymphoma.". Hematology Am Soc Hematol Educ Program: 349-58. doi:10.1182/asheducation-2008.1.349. PMID 19074109.
- ↑ Coso, D.; Rey, J.; Bouabdallah, R. (Feb 2010). "[Primary mediastinal B-cell lymphoma]". Rev Pneumol Clin 66 (1): 32-5. doi:10.1016/j.pneumo.2009.12.007. PMID 20207294.
- ↑ van Besien, K.; Kelta, M.; Bahaguna, P. (Mar 2001). "Primary mediastinal B-cell lymphoma: a review of pathology and management.". J Clin Oncol 19 (6): 1855-64. PMID 11251018.