Overview
Composite lymphoma is a rare hematologic malignancy defined by the simultaneous occurrence of two or more distinct types of lymphoma within the same patient, typically presenting in the same anatomical site (such as a single lymph node) or in different sites at the same time. Most commonly, composite lymphoma involves the coexistence of a Hodgkin lymphoma component alongside a non-Hodgkin lymphoma component, though combinations of two different non-Hodgkin lymphomas can also occur. The condition primarily affects the lymphatic system, including lymph nodes, spleen, and other lymphoid tissues, and may also involve extranodal sites such as the bone marrow, liver, or gastrointestinal tract. Patients typically present with painless lymphadenopathy (enlarged lymph nodes), and may experience constitutional symptoms such as unexplained fever, night sweats, unintentional weight loss, and fatigue — collectively known as B symptoms. The clinical course and prognosis depend on the specific histological subtypes involved, with the more aggressive component generally dictating the overall behavior of the disease. Diagnosis requires careful histopathological examination, often with immunohistochemistry and molecular studies, to confirm the presence of two distinct lymphoma populations rather than a single transformed lymphoma. Treatment of composite lymphoma is challenging because there is no standardized therapeutic protocol. Management is generally tailored to address the more aggressive lymphoma subtype, and may include combination chemotherapy regimens (such as ABVD for Hodgkin lymphoma components or R-CHOP for diffuse large B-cell lymphoma components), radiation therapy, immunotherapy, or stem cell transplantation in selected cases. Due to its rarity, evidence guiding treatment is largely derived from case reports and small case series, and multidisciplinary discussion is essential for optimal management. Prognosis varies widely depending on the specific lymphoma subtypes, stage at diagnosis, and response to therapy.
Also known as:
Sporadic
Usually appears on its own, not inherited from a parent
Adult
Begins in adulthood (age 18 or older)
FDA & Trial Timeline
1 eventM.D. Anderson Cancer Center — PHASE1, PHASE2
Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.
Treatments
1 availableBexxar
Treatment of patients with CD20 positive, follicular, non-Hodgkin's lymphoma, with and without transformation, whose disease is refractory to Rituximab and has relapsed following chemotherapy
Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Travel Grants
No travel grants are currently matched to Composite lymphoma.
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Caregiver Resources
NORD Caregiver Resources
Support, advocacy, and financial assistance for caregivers of rare disease patients.
Mental Health Support
Rare disease caregiving can be isolating. Connect with counseling and peer support.
Family & Caregiver Grants
Financial assistance programs specifically for caregivers of rare disease patients.
Social Security Disability
Learn how rare disease patients may qualify for SSDI/SSI benefits.
Common questions about Composite lymphoma
What is Composite lymphoma?
Composite lymphoma is a rare hematologic malignancy defined by the simultaneous occurrence of two or more distinct types of lymphoma within the same patient, typically presenting in the same anatomical site (such as a single lymph node) or in different sites at the same time. Most commonly, composite lymphoma involves the coexistence of a Hodgkin lymphoma component alongside a non-Hodgkin lymphoma component, though combinations of two different non-Hodgkin lymphomas can also occur. The condition primarily affects the lymphatic system, including lymph nodes, spleen, and other lymphoid tissues,
How is Composite lymphoma inherited?
Composite lymphoma follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.
At what age does Composite lymphoma typically begin?
Typical onset of Composite lymphoma is adult. Age of onset can vary across affected individuals.
Are there clinical trials for Composite lymphoma?
Yes — 1 recruiting clinical trial is currently listed for Composite lymphoma on UniteRare. See the clinical trials section on this page for phase, sponsor, and site details sourced from ClinicalTrials.gov.
Which specialists treat Composite lymphoma?
3 specialists and care centers treating Composite lymphoma are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.