Non-Hodgkin lymphoma diagnostic study of choice: Difference between revisions
Preeti Singh (talk | contribs) No edit summary |
No edit summary |
||
Line 3: | Line 3: | ||
==Overview== | ==Overview== | ||
The diagnostic study of choice for non-Hodgkin lymphoma is excisional lymph node biopsy. A bone marrow biopsy is an alternative to a lymph node biopsy. | The diagnostic study of choice for non-Hodgkin lymphoma is excisional lymph node biopsy. A bone marrow biopsy is an alternative to a lymph node biopsy. According to the Ann Arbor system with Cotswald modifications, there are four stages of non-Hodgkin lymphoma based on the number of nodes and extra nodal involvement. | ||
==Diagnostic study of choice== | ==Diagnostic study of choice== | ||
*The diagnostic study of choice for non-Hodgkin's lymphoma is excisional lymph node biopsy.<ref name="pmid28395545">{{cite journal| author=Jiang M, Bennani NN, Feldman AL| title=Lymphoma classification update: B-cell non-Hodgkin lymphomas. | journal=Expert Rev Hematol | year= 2017 | volume= 10 | issue= 5 | pages= 405-415 | pmid=28395545 | doi=10.1080/17474086.2017.1318053 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28395545 }} </ref> | *The diagnostic study of choice for non-Hodgkin's lymphoma is excisional lymph node biopsy.<ref name="pmid28395545">{{cite journal| author=Jiang M, Bennani NN, Feldman AL| title=Lymphoma classification update: B-cell non-Hodgkin lymphomas. | journal=Expert Rev Hematol | year= 2017 | volume= 10 | issue= 5 | pages= 405-415 | pmid=28395545 | doi=10.1080/17474086.2017.1318053 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28395545 }} </ref> | ||
Line 15: | Line 16: | ||
*Bilateral BM biopsy has been recommended with trephine biopsy being preferred to marrow aspiration for detecting marrow infiltration.<ref>Bartl R, Frisch B, Burkhardt R, Jδger K, Pappenberger R, Hoffmann-Fezer G. Lymphoproliferations in bone marrow: i0 dentification and evaluation, classification and staging. J Clin Pathol 1984;37:233-54.</ref><ref>Bain BJ, Clark DM, Lampert IA, Wilkins BS, editors. Bone marrow pathology. 3 rd ed. UK: Blackwell Science Ltd; 2001. </ref> | *Bilateral BM biopsy has been recommended with trephine biopsy being preferred to marrow aspiration for detecting marrow infiltration.<ref>Bartl R, Frisch B, Burkhardt R, Jδger K, Pappenberger R, Hoffmann-Fezer G. Lymphoproliferations in bone marrow: i0 dentification and evaluation, classification and staging. J Clin Pathol 1984;37:233-54.</ref><ref>Bain BJ, Clark DM, Lampert IA, Wilkins BS, editors. Bone marrow pathology. 3 rd ed. UK: Blackwell Science Ltd; 2001. </ref> | ||
*BM biopsies, performed under local anesthesia, were obtained using the conventional technique with a Jamshidi needle from the posterior superior iliac spines, fixed in 10% formalin solution and decalcified using 10% formal - formic acid for 4 - 6 h followed by routine processing and paraffin embedding.<ref>Culling CF, Allison RT, Barr WT. Connective tissue. In: Cellular Pathology Techniques. 4 th ed. London: Butterworth and Co. ltd; 1985. p. 172-3. </ref> | *BM biopsies, performed under local anesthesia, were obtained using the conventional technique with a Jamshidi needle from the posterior superior iliac spines, fixed in 10% formalin solution and decalcified using 10% formal - formic acid for 4 - 6 h followed by routine processing and paraffin embedding.<ref>Culling CF, Allison RT, Barr WT. Connective tissue. In: Cellular Pathology Techniques. 4 th ed. London: Butterworth and Co. ltd; 1985. p. 172-3. </ref> | ||
==Staging== | |||
According to the Ann Arbor staging system with Cotswald modifications, there are four stages of non-Hodgkin lymphoma based on the number of nodes and extra nodal involvement. | |||
Staging for non-Hodgkin lymphoma is provided in the following table:<ref name="pmid28287948">{{cite journal| author=Bligh MP, Borgaonkar JN, Burrell SC, MacDonald DA, Manos D| title=Spectrum of CT Findings in Thoracic Extranodal Non-Hodgkin Lymphoma. | journal=Radiographics | year= 2017 | volume= 37 | issue= 2 | pages= 439-461 | pmid=28287948 | doi=10.1148/rg.2017160077 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28287948 }} </ref><ref name="pmid28378140">{{cite journal| author=Thacker N, Bakhshi S, Chinnaswamy G, Vora T, Prasad M, Bansal D et al.| title=Management of Non-Hodgkin Lymphoma: ICMR Consensus Document. | journal=Indian J Pediatr | year= 2017 | volume= 84 | issue= 5 | pages= 382-392 | pmid=28378140 | doi=10.1007/s12098-017-2318-0 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28378140 }} </ref> | |||
{| style="border: 0px; font-size: 90%; margin: 3px;" align="center" | |||
|+ '''Ann Arbor staging system''' | |||
! style="background: #4479BA; color:#FFF;" | Stage | |||
! style="background: #4479BA; color:#FFF;" | Involvement | |||
|- | |||
| colspan="3" style="padding: 5px 5px; background: #DCDCDC;" | '''stage I''' | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | I | |||
| style="padding: 5px 5px; background: #F5F5F5;" | One nodal group or lymphoid organ (e.g. spleen or thymus) | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | IE | |||
| style="padding: 5px 5px; background: #F5F5F5;" | One extra nodal site | |||
|- | |||
| colspan="3" style="padding: 5px 5px; background: #DCDCDC;" | '''stage II''' | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | II | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Two or more nodal groups, same side of diaphragm | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | II E | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Localized extra nodal site with stage II criteria, both on the same side of the diaphragm | |||
|- | |||
| colspan="3" style="padding: 5px 5px; background: #DCDCDC;" | '''stage III''' | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | III | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Nodal groups on both sides of the diaphragm | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | III S (1) | |||
| style="padding: 5px 5px; background: #F5F5F5;" | With splenic involvement | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | III E (2) | |||
| style="padding: 5px 5px; background: #F5F5F5;" | With localized extra nodal site | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | III SE | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Both | |||
|- | |||
| colspan="3" style="padding: 5px 5px; background: #DCDCDC;" | '''stage IV''' | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | IV | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Disseminated involvement of one or more extra lymphatic organ (e.g. lung, bone) +/- any nodal involvement | |||
|- | |||
| colspan="3" style="padding: 5px 5px; background: #DCDCDC;" | '''Additional staging variables''' | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | X | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Bulky nodal disease: largest tumor is 10 cm or larger | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | A | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Asymptomatic | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | B | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Presence of B symptoms ([[fever]], [[night sweats]] and [[weight loss]]) | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | E | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Extra nodal: other than the lymph nodes or spread to tissues beyond, but nearby, the lymphatic tissues | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | S | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Spleen | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Limited disease | |||
| style="padding: 5px 5px; background: #F5F5F5;" | | |||
* Stage I or II<BR> | |||
* No B symptoms<BR> | |||
* Non-bulky tumor | |||
|- | |||
| style="padding: 5px 5px; background: #F5F5F5;" | Advanced disease | |||
| style="padding: 5px 5px; background: #F5F5F5;" | | |||
* Stage III or IV<BR> | |||
* B symptoms<BR> | |||
* Bulky tumor | |||
|} | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} |
Revision as of 19:32, 21 January 2019
Non-Hodgkin lymphoma Microchapters |
Differentiating Non-Hodgkin's Lymphoma |
---|
Treatment |
Case Studies |
Non-Hodgkin lymphoma diagnostic study of choice On the Web |
American Roentgen Ray Society Images of Non-Hodgkin lymphoma diagnostic study of choice |
Risk calculators and risk factors for Non-Hodgkin lymphoma diagnostic study of choice |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2]; Associate Editor(s)-in-Chief: Preeti Singh, M.B.B.S.[3]
Overview
The diagnostic study of choice for non-Hodgkin lymphoma is excisional lymph node biopsy. A bone marrow biopsy is an alternative to a lymph node biopsy. According to the Ann Arbor system with Cotswald modifications, there are four stages of non-Hodgkin lymphoma based on the number of nodes and extra nodal involvement.
Diagnostic study of choice
- The diagnostic study of choice for non-Hodgkin's lymphoma is excisional lymph node biopsy.[1]
- An excisional biopsy is needed because it preserves the architecture of the lymph node and allows for precise determination of the type of lymphoma.
- Fine needle aspiration biopsy is usually insufficient.[2]
- In addition to light microscopy evaluation of the excisional biopsy samples, the immunophenotypic analysis with immunohistochemistry helps to determine non-Hodgkin's lymphoma subtypes and distinguish non-Hodgkin's lymphoma from T cell rich large B cell lymphoma and anaplastic large cell lymphoma.[2]
- The presence of CD20 positive clonal B cells defines non-Hodgkin lymphoma.[3]
- In about 40% of adult patients with Non Hodgkin Lymphoma, the extranodal sites are the primary presenting sites with the most common site being the Gastrointestinal tract.[3]
- A bone marrow (BM) biopsy can also be done to diagnose non-Hodgkin lymphoma if there is sufficient evidence of marrow involvement such as presence of cytopenias.[3]
- Non-Hodgkin lymphoma cells originate in the bone marrow, which is the site of B cell production and maturation.
- Bilateral BM biopsy has been recommended with trephine biopsy being preferred to marrow aspiration for detecting marrow infiltration.[4][5]
- BM biopsies, performed under local anesthesia, were obtained using the conventional technique with a Jamshidi needle from the posterior superior iliac spines, fixed in 10% formalin solution and decalcified using 10% formal - formic acid for 4 - 6 h followed by routine processing and paraffin embedding.[6]
Staging
According to the Ann Arbor staging system with Cotswald modifications, there are four stages of non-Hodgkin lymphoma based on the number of nodes and extra nodal involvement. Staging for non-Hodgkin lymphoma is provided in the following table:[7][8]
Stage | Involvement | |
---|---|---|
stage I | ||
I | One nodal group or lymphoid organ (e.g. spleen or thymus) | |
IE | One extra nodal site | |
stage II | ||
II | Two or more nodal groups, same side of diaphragm | |
II E | Localized extra nodal site with stage II criteria, both on the same side of the diaphragm | |
stage III | ||
III | Nodal groups on both sides of the diaphragm | |
III S (1) | With splenic involvement | |
III E (2) | With localized extra nodal site | |
III SE | Both | |
stage IV | ||
IV | Disseminated involvement of one or more extra lymphatic organ (e.g. lung, bone) +/- any nodal involvement | |
Additional staging variables | ||
X | Bulky nodal disease: largest tumor is 10 cm or larger | |
A | Asymptomatic | |
B | Presence of B symptoms (fever, night sweats and weight loss) | |
E | Extra nodal: other than the lymph nodes or spread to tissues beyond, but nearby, the lymphatic tissues | |
S | Spleen | |
Limited disease |
| |
Advanced disease |
|
References
- ↑ Jiang M, Bennani NN, Feldman AL (2017). "Lymphoma classification update: B-cell non-Hodgkin lymphomas". Expert Rev Hematol. 10 (5): 405–415. doi:10.1080/17474086.2017.1318053. PMID 28395545.
- ↑ 2.0 2.1 Intragumtornchai T, Bunworasate U, Wudhikarn K, Lekhakula A, Julamanee J, Chansung K; et al. (2018). "Non-Hodgkin lymphoma in South East Asia: An analysis of the histopathology, clinical features, and survival from Thailand". Hematol Oncol. 36 (1): 28–36. doi:10.1002/hon.2392. PMID 28332735.
- ↑ 3.0 3.1 3.2 Casulo C, Burack WR, Friedberg JW (2015). "Transformed follicular non-Hodgkin lymphoma". Blood. 125 (1): 40–7. doi:10.1182/blood-2014-04-516815. PMID 25499449.
- ↑ Bartl R, Frisch B, Burkhardt R, Jδger K, Pappenberger R, Hoffmann-Fezer G. Lymphoproliferations in bone marrow: i0 dentification and evaluation, classification and staging. J Clin Pathol 1984;37:233-54.
- ↑ Bain BJ, Clark DM, Lampert IA, Wilkins BS, editors. Bone marrow pathology. 3 rd ed. UK: Blackwell Science Ltd; 2001.
- ↑ Culling CF, Allison RT, Barr WT. Connective tissue. In: Cellular Pathology Techniques. 4 th ed. London: Butterworth and Co. ltd; 1985. p. 172-3.
- ↑ Bligh MP, Borgaonkar JN, Burrell SC, MacDonald DA, Manos D (2017). "Spectrum of CT Findings in Thoracic Extranodal Non-Hodgkin Lymphoma". Radiographics. 37 (2): 439–461. doi:10.1148/rg.2017160077. PMID 28287948.
- ↑ Thacker N, Bakhshi S, Chinnaswamy G, Vora T, Prasad M, Bansal D; et al. (2017). "Management of Non-Hodgkin Lymphoma: ICMR Consensus Document". Indian J Pediatr. 84 (5): 382–392. doi:10.1007/s12098-017-2318-0. PMID 28378140.