Immunohistochemistry (IHC) is the tissue test that turns "this is a lymphoma" into a precise subtype diagnosis. It detects markers like CD20 and CD30 on your biopsy — and those markers shape exactly how your lymphoma is treated.
Immunohistochemistry — usually shortened to IHC — is a laboratory test performed on the tissue from your biopsy. It uses antibodies that latch onto specific proteins, called markers, on and inside the lymphoma cells. Wherever a marker is present, a colour develops that the pathologist can see under the microscope. In effect, IHC lets the lab "paint" the cells according to which proteins they carry.
This matters because most lymphomas look broadly similar on a plain stain. What separates one subtype from another is the pattern of markers they express. IHC is the step that turns a general finding — "this is a lymphoma" — into a precise subtype diagnosis. And the subtype decides almost everything that follows: whether the disease is slow-growing or aggressive, whether it is watched or treated promptly, and which class of therapy is likely to work.
IHC is run after your lymph node biopsy and is reported as part of your lymphoma pathology report. For the full picture of diagnosis and care, see our Lymphoma hub and Lymphoma Treatment in Hyderabad page.
Lymphoma is not one disease but a family of more than 60 distinct subtypes, each with its own behaviour and treatment. According to the current WHO classification of lymphoid tumours — referenced by both NCCN and ESMO — immunohistochemistry marker patterns are a defining part of how these subtypes are told apart. That is why a plain microscope slide is rarely enough on its own: it is the IHC marker panel that names the exact lymphoma. (Source: WHO Classification of Haematolymphoid Tumours, as referenced in NCCN and ESMO lymphoma guidelines.)
Getting the subtype right is the foundation of effective lymphoma care. CION builds every treatment plan on a complete, tissue-based diagnosis — never a rushed one.
IHC is done on the solid tissue slice, so our pathologists see the markers in place — how the cells are arranged and how fast they divide. This is combined with flow cytometry and immunophenotyping so nothing is missed. Together these tests are how doctors identify which lymphoma subtype you have.
Certain IHC markers in lymphoma do more than label the disease — they flag treatment targets. CD20 supports an anti-CD20 monoclonal antibody; CD30 identifies an antibody-based option in selected cases. Proliferation markers such as Ki-67 hint at how aggressive the disease is. We explain exactly what yours mean.
Your IHC result never stands alone. It is discussed by a multidisciplinary tumour board alongside staging, imaging, your LDH and other blood work — the standard NCCN and ESMO recommend — before a single treatment decision is made. See our lymphoma programme.
If IHC has already been done elsewhere, a re-read can confirm or refine the subtype. CION offers a free written second opinion from our lymphoma specialists — especially valuable if your report is unclear or key markers were not tested. Request one here.
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Just had a biopsy, holding a report full of markers like CD20 and CD30, or unsure your subtype is confirmed? CION's lymphoma team will read it with you.
IHC is a careful, multi-step process, which is part of why a full lymphoma diagnosis takes days rather than hours. In outline:
Because it works on the solid tissue, IHC keeps the tumour's architecture intact — a strength that a fluid-based test cannot match. It is frequently paired with flow cytometry, and, when needed, with molecular and genetic testing.
No single marker gives the diagnosis — the pathologist reads the whole pattern. This table shows some of the most common markers and what a positive result typically points to.
| Marker | Points towards | Why it matters |
|---|---|---|
| CD20 | B-cell lymphoma | Confirms B-cell origin; flags an anti-CD20 monoclonal antibody as a treatment target |
| CD3, CD5 | T-cell lymphoma | Identify a T-cell origin, a distinct group with different treatment |
| CD30 | Classic Hodgkin & some large-cell lymphomas | Strongly positive in classic Hodgkin lymphoma; also an antibody-based treatment target |
| CD15 | Classic Hodgkin lymphoma | Supports a Hodgkin diagnosis alongside CD30 |
| CD10, BCL6 | Germinal-centre origin | Help sub-classify B-cell lymphomas and estimate behaviour |
| MYC, BCL2 | Aggressive B-cell disease | May trigger molecular testing for "double-hit" lymphoma |
| Ki-67 | Proliferation rate | A high figure suggests faster-growing, more aggressive disease |
This is a general guide, not a diagnosis. The exact panel and its interpretation vary by case and are decided by a pathologist. Marker naming follows the WHO classification, as referenced in NCCN and ESMO lymphoma guidelines.
Among the CD20, CD30 lymphoma markers, these two come up often because they do double duty: they help diagnose the subtype and they point to therapy.
CD20 sits on the surface of most B cells. When a lymphoma is CD20-positive, it confirms a B-cell origin and tells the team that an anti-CD20 monoclonal antibody — a class of immunotherapy delivered directly at CION — may form part of treatment. Because so many common lymphomas are CD20-positive, this single marker often shapes the therapeutic approach.
CD30 is strongly positive in classic Hodgkin lymphoma and in some aggressive T-cell and large-cell lymphomas. As with CD20, its value is twofold: it supports the diagnosis and identifies an antibody-based treatment target in selected cases. Your oncologist will explain whether your CD30 status opens up such an option.
Note: markers describe what class of therapy may help. Specific drug names and regimens are always individualised and are discussed on our Lymphoma Treatment in Hyderabad page, not decided from a marker alone.
Outcomes in lymphoma depend heavily on the subtype that IHC identifies. Published series show Hodgkin lymphoma carries roughly 80–90% long-term survival, while diffuse large B-cell lymphoma sits around 60–70% in many series (per NCCN and ESMO data). These are averages across large groups — figures vary considerably by individual, stage, age and overall fitness. The point is not the exact number but why the subtype matters: naming it accurately with IHC is what makes it possible to choose the treatment most likely to help.
IHC is one important piece of a bigger picture. A full lymphoma diagnosis and plan usually draws on several tests, each answering a different question:
All of these come together in your pathology report and are reviewed as one. If an enlarged node was found on a scan or a report mentions bulky disease, the same principle applies — the tissue diagnosis leads.
Because the subtype drives the entire plan, a second opinion on the pathology is especially worthwhile in a few situations:
CION offers a dedicated, free written second-opinion service with transparent costs explained up front — a plan built around healing, not billing. Request your free second opinion or call 18002028726.
Get a free written second opinion from CION's lymphoma tumour board — especially valuable if your IHC panel was limited or the report is unclear.
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Start Your Story. Book Free Consultation.Immunohistochemistry, or IHC, is a laboratory test done on your biopsy tissue that uses antibodies to detect specific proteins — called markers — on and inside the lymphoma cells. Under the microscope, cells that carry a marker turn a visible colour, so the pathologist can literally see which proteins the tumour expresses. This matters because lymphomas look broadly similar under a plain stain, but different subtypes carry very different marker patterns. IHC is the step that turns "this is a lymphoma" into a precise subtype diagnosis, which then guides the whole treatment plan. It is performed after your lymph node biopsy and reported as part of your pathology report.
A standard lymphoma panel usually starts with markers that separate B-cell from T-cell lymphomas and both from Hodgkin lymphoma. Common IHC markers in lymphoma include CD20 and CD79a (B cells), CD3 and CD5 (T cells), CD30 and CD15 (classic Hodgkin lymphoma), CD10 and BCL6 (germinal-centre origin), BCL2, MYC, cyclin D1, Ki-67 (a proliferation marker), and CD23. No single marker gives the answer — the pathologist reads the whole pattern of positive and negative stains. The exact panel is chosen for what the case looks like, so two people can have quite different panels. IHC is often combined with flow cytometry and immunophenotyping for a complete picture.
CD20 and CD30 are two of the most talked-about markers. CD20 is a protein found on most B cells; when a lymphoma is "CD20-positive" it confirms a B-cell origin and, importantly, tells the team an anti-CD20 antibody (a class of immunotherapy) may be part of treatment. CD30 is strongly positive in classic Hodgkin lymphoma and in some aggressive T-cell and large-cell lymphomas; it also identifies a target for an antibody-based therapy in selected cases. So CD20 and CD30 in lymphoma are not just diagnostic labels — they flag treatment targets. Your oncologist explains exactly what your markers mean for you; specific drug regimens are discussed on our Lymphoma Treatment in Hyderabad page.
Both look at cell-surface and internal markers, but in different ways. IHC is done on the solid tissue slice, so the pathologist sees the markers in their tissue context — how the cells are arranged, whether they sit in the right structures, and their proliferation rate. Flow cytometry runs a fluid suspension of cells through a laser and measures many markers per cell very quickly and quantitatively, which is excellent for blood, bone marrow and fresh tissue. They are complementary, not competing: IHC preserves architecture, flow adds speed and precise co-expression data. Read more on flow cytometry and immunophenotyping, and how both feed into identifying your lymphoma subtype.
IHC does not by itself decide treatment, but it is one of the biggest inputs. The marker pattern establishes the subtype, and certain markers point to targeted options — for example CD20 positivity supports adding an anti-CD20 monoclonal antibody, while proliferation markers such as Ki-67 hint at how aggressive the disease is. Markers like MYC and BCL2 may prompt further molecular and genetic testing (for "double-hit" disease or cell of origin). The final plan combines the IHC subtype, stage, your LDH and other blood results, imaging and your overall health, and is reviewed by a multidisciplinary tumour board. Actual drug regimens are covered on the Treatment page.
A basic microscopic (H&E) assessment of a lymph node is often available within a couple of days, but a full lymphoma diagnosis usually takes longer because IHC is a multi-step process: the tissue is fixed, sectioned, stained with a panel of antibodies, and then interpreted — and the pathologist frequently orders a second round of markers once the first results come back. In practice, a complete IHC-based lymphoma report commonly takes about five to ten working days, and longer if molecular testing is added. The wait can feel long, but a precise subtype is what makes treatment effective, so it is time well spent. If you are waiting on a report, our team can review it with you — book a free consultation.
Because "lymphoma" is not one disease — it is a family of more than 60 subtypes, each with its own behaviour, treatment and outlook. IHC is central to telling them apart. Getting the subtype right changes everything: an indolent lymphoma may be safely monitored, while an aggressive one needs prompt combination therapy; a CD20-positive B-cell lymphoma may benefit from an antibody a T-cell lymphoma would not. Published series show outcomes differ widely by subtype — Hodgkin lymphoma carries roughly 80–90% long-term survival and diffuse large B-cell lymphoma roughly 60–70% in many series (per NCCN and ESMO data), though figures vary by individual, stage and fitness. This is exactly why CION insists on a full IHC-based diagnosis before treatment, coordinated through our lymphoma programme.
Browse our complete guide to lymphoma — symptoms, diagnosis, Hodgkin and non-Hodgkin subtypes, treatment, genetics, prognosis, survivorship and cost. Tap any topic to read more.