The Roundup litigation compensates one family of cancers: non-Hodgkin lymphoma. But if that were the end of the answer, this page would not need to exist. “Non-Hodgkin lymphoma” is not a single disease — it is an umbrella over roughly seventy separately named blood cancers, and your pathology report almost certainly uses one of the specific names, not the umbrella. Every subtype below is on the qualifying list used in the litigation, as updated in February 2026. If any of these names — or any of the older names in parentheses — appears in your records or a family member’s, call me at (402) 378-9208 for a free case review, and read the Roundup claims page for how the rest of the case works.
Why the Name on Your Pathology Report Matters
Here is the conversation I have had too many times. Someone calls about a spouse’s leukemia, apologizes for bothering me, and says they assume Roundup cases are only for “lymphoma.” Then I ask what the pathology report says, they read me chronic lymphocytic leukemia, and I get to tell them that CLL is on the list — it is a non-Hodgkin lymphoma in everything but its everyday name. The naming of blood cancers is genuinely confusing: the same disease can be called a leukemia when it lives in the blood and a lymphoma when it lives in the nodes, diseases have been renamed repeatedly as classification systems evolved, and a diagnosis written in 1998 may use a term no oncologist would write today. That is why the list below includes the also-known-as names — the older labels that appear in older records — and why the only reliable way to answer “do I qualify?” is to read the actual words on the actual report.
Two housekeeping notes before the list. First, this page is legal information, not medical advice — your oncologist defines your diagnosis; my job is what the diagnosis qualifies for. Second, the list distinguishes aggressive from indolent subtypes. That is a clinical distinction about how the disease behaves — fast-moving versus slow-growing — and both categories qualify. It can affect how a claim is valued and handled, which is a conversation for the phone, not a reason to hesitate before calling.
Check Your Diagnosis
The fastest way to use this page: type any part of the diagnosis from your pathology report — “follicular,” “CLL,” “large B-cell,” “mantle” — and the list below will narrow to what matches, older names included.
Aggressive Subtypes on the Qualifying List
The fast-moving diseases — the ones that announce themselves and send you to treatment quickly. Diffuse large B-cell lymphoma, the most common non-Hodgkin lymphoma in adults, leads this category.
- Adult T-cell leukemia/lymphoma (high grade or other features present)
- Aggressive NK-cell leukemia (a/k/a aggressive NK-cell leukaemia/lymphoma)
- ALK-positive large B-cell lymphoma (a/k/a large B-cell lymphoma expressing the ALK kinase and lacking the t(2;5) translocation; ALK-positive plasmablastic B-cell lymphoma)
- Anaplastic large cell lymphoma, ALK-negative
- Anaplastic large cell lymphoma, ALK-positive (a/k/a Ki-1 lymphoma)
- B-cell prolymphocytic leukemia (ICC); splenic B-cell lymphoma/leukemia with prominent nucleoli (WHO) (a/k/a prolymphocytic leukaemia, B-cell type)
- B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormalities
- B-lymphoblastic leukemia/lymphoma, not otherwise specified (a/k/a B-cell acute lymphoblastic leukaemia (B-ALL); pre-B lymphoblastic leukaemia; precursor B-lymphoblastic leukaemia/lymphoma; pro-B lymphoblastic leukaemia)
- Breast implant–associated anaplastic large cell lymphoma (high grade or other features present; a/k/a seroma-associated anaplastic large cell lymphoma)
- Burkitt lymphoma (a/k/a Burkitt tumour; malignant lymphoma, undifferentiated, Burkitt type; Burkitt cell leukaemia)
- Diffuse large B-cell lymphoma (DLBCL), NOS (a/k/a immunoblastic lymphoma (IBL))
- Diffuse large B-cell lymphoma associated with chronic inflammation (a/k/a pyothorax-associated lymphoma)
- EBV-positive diffuse large B-cell lymphoma, NOS (a/k/a EBV-positive DLBCL of the elderly; age-related EBV-positive lymphoproliferative disorder)
- EBV-positive polymorphic B-cell lymphoproliferative disorder, NOS (high grade or other features present)
- EBV-positive T-cell and NK-cell lymphoproliferative diseases of childhood (a/k/a Epstein-Barr virus (EBV) T-cell lymphoproliferative disease of childhood; fulminant EBV-positive T-cell lymphoproliferative disorder of childhood; sporadic fatal infectious mononucleosis)
- Extranodal NK/T-cell lymphoma, nasal type (a/k/a angiocentric T-cell lymphoma; polymorphic reticulosis; lethal midline granuloma; T/NK cell lymphoma)
- Follicular helper T-cell lymphoma, including angioimmunoblastic T-cell lymphoma
- Hepatosplenic T-cell lymphoma (a/k/a hepatosplenic gamma/delta T-cell lymphoma)
- HHV-8 and EBV-negative primary effusion-based lymphoma
- HHV8-associated lymphoproliferative disorders, including primary effusion lymphoma (a/k/a large B-cell lymphoma arising in HHV8-associated multicentric Castleman disease; HHV8-positive plasmablastic lymphoma)
- High-grade B-cell lymphoma with MYC and BCL2 rearrangements (a/k/a double-hit lymphoma)
- High-grade B-cell lymphoma with MYC and BCL6 rearrangements (ICC) (a/k/a double-hit lymphoma)
- High-grade B-cell lymphoma, not otherwise specified (a/k/a B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and Burkitt lymphoma)
- Immunodeficiency-associated lymphoproliferative disorders (lymphoproliferative disorders and lymphomas associated with primary immune disorders or HIV infection, following transplantation, and/or iatrogenic)
- Intravascular large B-cell lymphoma (a/k/a angiotropic large cell lymphoma; malignant angioendotheliomatosis; intravascular lymphomatosis)
- Large B-cell lymphoma with 11q aberration
- Large B-cell lymphoma with IRF4 rearrangement
- Mantle cell lymphoma: conventional and leukemic non-nodal subtypes (a/k/a mantle zone lymphoma; malignant lymphoma, centrocytic; malignant lymphomatous polyposis)
- Mediastinal gray zone lymphoma (a/k/a B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and classical Hodgkin lymphoma; large B-cell lymphoma with Hodgkin’s features)
- Monomorphic epitheliotropic intestinal T-cell lymphoma (a/k/a intestinal T-cell lymphoma)
- Mycosis fungoides (high grade or other features present)
- NK-lymphoblastic leukemia/lymphoma
- Peripheral T-cell lymphoma, NOS (a/k/a peripheral T-cell lymphoma, unspecified; T-cell lymphoma, NOS; lymphoepithelioid lymphoma; Lennert lymphoma)
- Plasmablastic lymphoma
- Primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma
- Primary cutaneous diffuse large B-cell lymphoma, leg type
- Primary cutaneous gamma-delta T-cell lymphoma
- Primary diffuse large B-cell lymphoma of the CNS (a/k/a primary CNS lymphoma; primary intraocular lymphoma; lymphomatosis cerebri)
- Primary diffuse large B-cell lymphoma of the testis
- Primary mediastinal large B-cell lymphoma (a/k/a mediastinal (thymic) large B-cell lymphoma; mediastinal diffuse large cell lymphoma with sclerosis)
- Primary nodal EBV-positive T-cell/NK-cell lymphoma
- Sézary syndrome
- T-cell prolymphocytic leukemia (a/k/a prolymphocytic leukaemia, T-cell type; T-cell chronic lymphocytic leukemia)
- T-cell/histiocyte-rich large B-cell lymphoma (a/k/a T-cell-rich large B-cell lymphoma; (large) B-cell lymphoma rich in T-cells and simulating Hodgkin disease)
- T-lymphoblastic leukemia/lymphoma (a/k/a precursor T-lymphoblastic leukaemia/lymphoma; T acute lymphoblastic leukaemia (T-ALL))
- Type II refractory celiac disease and enteropathy-associated T-cell lymphoma (a/k/a enteropathy-associated T-cell lymphoma; enteropathy-type intestinal T-cell lymphoma; malignant histiocytosis of the intestine)
Indolent Subtypes on the Qualifying List
The slow-growing diseases — often found on routine bloodwork, sometimes watched for years before treatment. Do not let the gentler clinical course fool you into thinking these matter less legally: CLL/SLL and follicular lymphoma are among the most commonly diagnosed qualifying cancers in farm country.
- Adult T-cell leukemia/lymphoma (localized)
- BCL2-rearrangement negative, CD23-positive follicular lymphoma (ICC)
- Breast implant–associated anaplastic large cell lymphoma (localized; a/k/a seroma-associated anaplastic large cell lymphoma)
- Chronic lymphocytic leukemia / small lymphocytic lymphoma (CLL/SLL) (a/k/a chronic lymphocytic leukaemia, B-cell type; chronic lymphoid leukaemia; chronic lymphatic leukaemia)
- Chronic lymphoproliferative disorder of NK cells (a/k/a chronic NK-cell lymphocytosis; NK-cell LGL lymphocytosis; indolent leukaemia of NK cells)
- Duodenal-type follicular lymphoma (WHO)
- Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) (a/k/a extranodal marginal zone B-cell lymphoma; gastric MALT)
- Follicular lymphoma
- Hairy cell leukemia (a/k/a leukaemic reticuloendotheliosis)
- Lymphoplasmacytic lymphoma / Waldenström macroglobulinemia (a/k/a lymphoplasmacytoid lymphoma)
- Mycosis fungoides (localized)
- Nodal marginal zone lymphoma (a/k/a monocytoid B-cell lymphoma; parafollicular B-cell lymphoma)
- Nodular lymphocyte predominant B-cell lymphoma (ICC) (a/k/a nodular lymphocyte predominant Hodgkin lymphoma; L&H Hodgkin lymphoma)
- Pediatric nodal marginal zone lymphoma (WHO)
- Pediatric-type follicular lymphoma
- Primary cutaneous acral CD8-positive T-cell lymphoproliferative disorder
- Primary cutaneous CD30-positive T-cell lymphoproliferative disorders; primary cutaneous anaplastic large-cell lymphoma
- Primary cutaneous CD4-positive small/medium T-cell lymphoproliferative disorder
- Primary cutaneous follicle center lymphoma (a/k/a Crosti’s disease; Crosti lymphoma)
- Primary cutaneous marginal zone lymphoma
- Splenic B-cell lymphoma/leukaemia, unclassifiable (a/k/a prolymphocytic variant of hairy cell leukemia; splenic red pulp lymphoma with numerous basophilic villous lymphocytes; splenic B-cell lymphoma with villous lymphocytes)
- Splenic marginal zone lymphoma (a/k/a splenic B-cell marginal zone lymphoma; splenic lymphoma with villous lymphocytes)
- Subcutaneous panniculitis-like T-cell lymphoma
- T-cell large granular lymphocytic leukemia (a/k/a T-cell large granular lymphocytosis; T-gamma lymphoproliferative disease)
- Testicular follicular lymphoma
How to Read the Fine Print in the List
A few markings above deserve translation. Where an entry carries a (WHO) or (ICC) tag, it means the diagnosis is named under one of the two modern classification systems pathologists use — the World Health Organization’s scheme or the International Consensus Classification — and your report may cite either; both count. Where an entry is qualified localized or high grade or other features present, the same disease appears in both halves of the list, sorted by how it presented — adult T-cell leukemia/lymphoma, mycosis fungoides and breast implant–associated lymphoma all straddle the line, qualifying either way. And the semicolons inside entries separate genuinely interchangeable names for one disease: if your report matches any name in an entry, it matches the entry. None of this fine print exists to trip patients — it exists because pathology reports span forty years of changing vocabulary, and the list is built to catch every version of the words.
The Diagnoses People Don’t Realize Count
A few entries above deserve to be pulled out of the list, because they are the ones qualifying Nebraskans most often dismiss:
- Chronic lymphocytic leukemia (CLL). The word “leukemia” convinces people they are outside the lymphoma litigation. They are not — CLL and small lymphocytic lymphoma are the same disease in different tissue, and both are on the list.
- Hairy cell leukemia. Same story — a B-cell cancer squarely on the list, hiding behind a leukemia name.
- Waldenström macroglobulinemia. Most patients have never heard it called lymphoplasmacytic lymphoma, which is what it is.
- The skin lymphomas. Mycosis fungoides, Sézary syndrome, and the primary cutaneous lymphomas are diagnosed by dermatologists as often as oncologists, and patients frequently never connect a “skin condition” to the lymphoma litigation.
- The pediatric subtypes. Children who grew up on and around sprayed ground appear on this list too — pediatric-type follicular lymphoma, pediatric nodal marginal zone lymphoma, and the childhood EBV-associated diseases.
What About Hodgkin Lymphoma, Myeloma, and Everything Else?
Honesty is the policy on this site, so: classical Hodgkin lymphoma is not on the qualifying list, and neither is multiple myeloma. One nuance matters, though — nodular lymphocyte predominant disease, which older records call “nodular lymphocyte predominant Hodgkin lymphoma,” has been reclassified by modern pathology as a B-cell lymphoma and is on the list. That is the single best illustration of why you should never disqualify yourself based on a disease name: a diagnosis with “Hodgkin” in its historical name qualifies because of what the disease actually is. And if your cancer is not on this list at all, a call may still be worth your time — other exposures carry other claims: asbestos and mesothelioma, benzene-linked leukemias, and the industrial and railroad occupational cancers I handle under different laws.
How to Find the Magic Words in Your Records
The document you want is the surgical pathology report — the report generated when your biopsy was read — and after it, the oncologist’s initial consultation note. Look for the line labeled “diagnosis” or “final diagnosis.” It will name the subtype, often with a WHO or ICC classification reference, sometimes with immunophenotype codes (CD20-positive, CD30, ALK) that also appear in the list above. If you cannot find the report, do not let that stop you from calling: you are entitled to your records, requests are routine, and I make them for my clients every week. For a family member who has died, the records survive and remain reachable — a personal representative can obtain them, and I help families do exactly that in wrongful-death reviews.
The Second Half of Qualifying: Exposure
The diagnosis is one pillar; Roundup exposure is the other. On this, one sentence here and the full story on the claims page: you did not have to be the person spraying — living beside sprayed fields, years around a treated golf course, park or campus, farm work near the product, and long-running home use can all qualify, and in Nebraska and Iowa that describes an enormous number of ordinary lives. Diagnosis from this page plus history like that equals a phone call worth making.
A Note on This List’s Currency
Blood-cancer classification is a moving target — the WHO and ICC systems continue to rename and split diagnoses, and the litigation’s qualifying list gets updated to follow. The version above reflects the February 2026 update, which is the current one as I write this. If your diagnosis sits near an edge — an unusual variant, a name you cannot find here, a report older than the modern classifications — do not adjudicate it yourself with a search engine. Read me the report. It costs nothing, it takes minutes, and being wrong in the cautious direction costs families real money.
Your Attorney
Frank Younes
Every page on this site is written by Frank Younes, a Nebraska trial attorney with a published record of verdicts and settlements, selection to the National Trial Lawyers Top 100, and a practice that covers every county in Nebraska and Iowa. No case is handed to an associate — the lawyer you read here is the lawyer who works your case.
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Frequently Asked Questions
My diagnosis says “leukemia,” not “lymphoma.” Am I excluded?
No — several leukemias are non-Hodgkin lymphomas by another name and are on the list: CLL, hairy cell leukemia, T-cell prolymphocytic leukemia, and the lymphoblastic leukemia/lymphomas among them. Read me the exact words on your pathology report.
Does classical Hodgkin lymphoma qualify?
No — classical Hodgkin lymphoma is not on the qualifying list. But nodular lymphocyte predominant disease, historically called a Hodgkin lymphoma, is now classified as a B-cell lymphoma and does appear on the list. Names mislead; reports decide.
My report just says “diffuse large B-cell lymphoma.” Is that enough?
Yes — DLBCL, NOS is on the list; it is the most common adult non-Hodgkin lymphoma. The next question is your exposure history, which the free review covers.
Do I need to know my subtype before calling?
No. “Non-Hodgkin lymphoma” from your doctor is enough to start, and I can obtain the pathology report that pins down the subtype. Do not let a missing document delay a phone call that is free.
Does it matter whether my subtype is aggressive or indolent?
Both categories qualify. The distinction describes the disease’s clinical behavior and can factor into how a claim is valued, but it is never a reason not to call.
I’m in remission. Do I still qualify?
Remission does not erase the diagnosis or the claim — you lived through the disease, its treatment and its costs. Timing rules still apply, so call sooner rather than later.
More on Toxic Exposure
The rest of the exposure series on this site.
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