Difference between revisions of "Haematopathology"
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==Lymphoma== | ==Lymphoma== | ||
{{main|Lymphoma}} | {{main|Lymphoma}} | ||
==Myeloproliferative neoplasms== | |||
{{main|Myeloproliferative neoplasms}} | |||
This subset of haematopathology includes, among others, polycythemia vera. | |||
==Plasma cell lesions== | ==Plasma cell lesions== | ||
Revision as of 14:09, 4 May 2011
Understanding of haematopathology is important in anatomical pathology, as haematologic malignancies are often in the (clinical) differential diagnosis and may mimic small blue round cell tumours or lobular breast carcinoma.
The lymph node is discussed below; however, details are covered in the lymph node article and lymph node pathology article.
Bone marrow
Bone marrows are important for understanding haematopathology. They are dealt with in the bone article.
Normal lymph node
Microscopic
The microscopic lymph node architecture in described the lymph node article, along with B cell maturation and lymph node cell types.
The cells of the lymph node:
- Germinal center:
- Centrocytes - cleaved nucleus.
- Centroblasts - large dark, mitotically active, medullary aspect of germinal center.
- Tingible body macrophages.
- Follicular dendritic cells.
- Paracortex:
- T lymphocytes.
- Interdigitating dendritic cells.
- Mantle zone:
- Immunoblasts (Memory B cells) - small lymphocytes.
- Medulla:
- B lymphocytes.
- Plasma cells.
Hemophagocytic syndrome
General
- Rare.
Microscopic
Features:
- Macrophages eat RBCs, WBCs.
Heparin-induced thrombocytopenia
- Thrombocytopenia due to heparin.[1]
Classification:
- Type 1 - in first two days of exposure - considered non-immune and considered not to be serious.
- Type 2 - in the first 4-10 days - considered serious.
Diagnosis (simplified):
- 50% decline in platelets - within 4-10 days of starting heparin.
- HIT assay - several exist.[2]
Disseminated intravascular coagulation
General
- Commonly abbreviated DIC.
- Usually associated with sepsis or septic shock.[3]
Clinical:
- Schistocytes (red blood cell fragmentation).
Gross
Features:[4]
- Pleural petechial haemorrhages.
Microscopic
Features:[5]
- Microvascular occlusion.
Notes:
- Microvascular occlusion is also seen in thrombotic microangiopathies.
Lymphoma
Myeloproliferative neoplasms
This subset of haematopathology includes, among others, polycythemia vera.
Plasma cell lesions
- See the lymphoma article.
Cytometry - population cell marker quantification
Two techniques
- Flow cytometry.
- Laser scanning cytometry (LSC).
Common markers
- CD3, CD4, CD8, CD5, CD7.
- CD19, CD20, FMC7.
- Kappa, lambda.
Normal
- T-cells to B-cells usually 1:1.
- In reactive nodes T-cells predominate.
- Normal thymic tissue has cells that are positive for both CD4 and CD8.
- Kappa (k) and lambda (l) are not expressed by the same cell.
- Rule-of-thumb for normal k:l range is: <6:1 and 1:<3.[6]
- Lambda dominance is less common.
GS guidelines - non-malignant is:[7]
- CD19 ~= CD20.
- CD5 = CD3.
- CD2 > CD3 and CD5.
- CD4 + CD8 ~= CD3.
- CD7 = the smallest number of T-cell.
Abnormal
See cytometry.
See also
References
- ↑ http://emedicine.medscape.com/article/1357846-overview
- ↑ http://emedicine.medscape.com/article/1357846-diagnosis
- ↑ URL: http://emedicine.medscape.com/article/779097-overview. Accessed on: 23 October 2010.
- ↑ Burton, Julian L.; Rutty, Guy N. (2010). The Hospital Autopsy A Manual of Fundamental Autopsy Practice (3rd ed.). Oxford University Press. pp. 209. ISBN 978-0340965146.
- ↑ Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 670. ISBN 978-1416031215.
- ↑ SB. March 10, 2010.
- ↑ GS. LSC Procedure. March 11, 2010.