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Primary Bone Lymphoma

A rare lymphoma subtype presenting primarily in bone, often mimicking other primary bone tumours.


Epidemiology

  • Accounts for 3–7% of all primary malignant bone tumors.

  • About 5% of extranodal lymphomas, but <1% of all Non-Hodgkin lymphomas (NHL).

  • Predominantly affects 20–50 years, with male preponderance.

  • Femur most common site (~29%), followed by tibia, pelvis, and spine.

  • Rare presentations: solitary lesions in the skull.


Etiology

  • Mostly non-Hodgkin B-cell lymphomas (DLBCL commonest).

  • Rarely T-cell variants.

  • Genetic predisposition and viral infections (EBV) implicated.

  • Classified as:
    Solitary bone site
    Multiple bone sites
    Bone + soft tissue lymphoma


Clinical Presentation

  • Bone pain unrelieved by rest (most common).

  • ~25% present with pathological fracture.

  • Neurological symptoms if spine involved.

  • Systemic symptoms: fever, weight loss, night sweats.


  Imaging

  • X-ray: variable → from near-normal to lytic, mixed lytic-sclerotic, or permeative lesions ± soft tissue mass.

  • MRI, PET-CT, CT: essential for marrow infiltration, extraosseous spread, treatment response.

  • Differential diagnosis: osteomyelitis, multiple myeloma, metastasis.


 Pathology

  • Diagnosis: biopsy + bone marrow aspiration.

  • Histology:
    Diffuse large B-cell lymphoma (DLBCL) most frequent.
    IHC: CD20+, CD45+, LCA+.
    “Small round blue cell” infiltration possible.

 

Treatment

  • Multidisciplinary approach: systemic chemotherapy + local radiotherapy.

  • CHOP-like regimens (anthracyclines, cyclophosphamide) = mainstay.

  • Chemotherapy alone effective for most lesions.

  • Surgery: reserved for pathological fracture fixation or stabilization.


 References

  1. Beal K, Allen L, Yahalom J. Primary bone lymphoma: treatment results and prognostic factors with long-term follow-up of 82 patients. Cancer. 2006;106(12):2652-6.

  2. Jawad MU, Schneiderbauer MM, Min ES, Cheung MC, Koniaris LG, Scully SP. Primary lymphoma of bone in adult patients. Cancer. 2010;116(4):871-9.

  3. Messina C, Christie D, Zucca E, Gospodarowicz M, Ferreri AJM. Primary and secondary bone lymphomas. Cancer Treat Rev. 2015;41(3):235-46.

  4. Ramadan KM, Shenkier T, Sehn LH, Gascoyne RD, Connors JM. A clinicopathological retrospective study of 131 patients with primary bone lymphoma: a population-based study of successively treated cohorts from the British Columbia Cancer Agency. Ann Oncol. 2007;18(1):129-35.

  5. Fletcher CDM, Bridge JA, Hogendoorn P, Mertens F, eds. WHO Classification of Tumours of Soft Tissue and Bone. 5th ed. Lyon: IARC Press; 2020.


Conventional osteosarcoma of the left thigh encasing femoral vessels and invading muscle planes; managed with left hip disarticulation after multidisciplinary evaluation.
Pleomorphic sarcoma of the left arm diagnosed by imaging and biopsy; treated with limb-salvage surgery and wide resection.
Synovial sarcoma was confirmed through imaging and biopsy. The patient underwent limb-salvage surgery with wide excision and free flap reconstruction.
humerus im nailing
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