pediatric lymphomas


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pediatric lymphomas

  1. 1. Pediatric Lymphomas Resident Education Lecture Series
  2. 2. Cervical adenopathy
  3. 3. Concerns in enlarged LN     Size >1-2 cm Increasing size over 2-4 weeks Matted or fixed Supraclavicular LN    Fevers >38.5 for 2-4 weeks Constitutional symptoms HSM
  4. 4. When to biopsy     Supraclavicular node Increasing size over 2-4 weeks Constitutional symptoms Asymptomatic enlarged nodenot decreasing in size over 6 weeks or not normal after 8-12 weeks
  5. 5. Staging Evaluation Laboratory -CBC with smear -Chem profile LHD, uric acid  Disease specific -ESR, IL2R for HD -LP if head/neck NHL -BMA/Bx for all NHL, only IIB or higher HD  Radiology -CXR (PA & Lat) -CT scans neck, chest, abdomen -Gallium, bone scan -PET scan 
  6. 6. Lymphoma Staging         Murphy ≈ Ann Arbor I: tumor at one site (nodal or extranodal -- “E”) II: two or more sites; same side of body (or resectable GI primary) III: both sides of body but not IV (& unresec. GI & mediastinal for NHL) IV: CNS or marrow involvement (Murphy); lung, liver, marrow, or bone for Ann Arbor (< 25% marrow) “B” sxs are defined for HD, as is “bulky disease” Head and neck (possibility of CNS involvement) is a further consideration for NHL PET or gallium
  8. 8. Non-Hodgkin’s Lymphoma Malignant solid tumor of immune system Undifferentiated lymphoid cells Spread: aggressive, diffuse, unpredictable Lymphoid tissue; BM and CNS infiltration High growth fraction and doubling time Dx and Rx ASAP Rapid CTX response; tumor lysis concern
  9. 9. Incidence/Etiology - NHL 6% childhood cancer 60% of childhood lymphomas Peak age of 5-15; M:F ratio of 2.5:1 Increased with SCIDS, HIV, EBV post t-cell depleted BMT post solid organ transplant Geographic, viral, genetic & immunologic factors
  10. 10. Types of NHL Lymphoblastic (30-35%)  90 % immature T cells (very similar to T-ALL)     remainder pre-B phenotype (as in ALL) 50-70% anterior mediastinum neck, supraclavicular, axillary adenopathy Classic: older child with intussusception
  11. 11. Small non-cleaved cell (40-50%) --Mature B-cell phenotype --Burkitt's and non-Burkitt's --90% abdomen --Ascites and intusussception --Endemic in Africa (Burkitt's), with EBV 97%
  12. 12. Burkitt Facts    100 new cases/year in US, 2-3:1 male:female; mean age 11 years (in non-endemic form) small, noncleaved cell; mature B phenotype; intraabdominal (sporadic) or jaw (endemic) most common primary site 90% have t(8;14)   others are 8;2 or 8;22   (8 ~ c-myc; 14 ~ heavy chains) (2, 22 ~ light chains) Extremely rapidly-growing; tumor lysis issues
  13. 13. Burkitt Prognosis Adult Data: Stage: EFS OS I-II 91% 78% IV 25% 25% but in patients < 40 yo 70% 60% Pediatric Data: Localized > 90% Disseminated (but not B- ALL) 80-90% on newer protocols
  14. 14. Large-cell lymphoma (15-20%) - Anaplastic (Ki-1) lymphoma – ALK fusion protein - Diffuse Large B-cell lymphoma (DLBCL) - - frequent Mediastinal involvement More like Hodgkin lymphoma than other NHLs “Peripheral T-cell” lymphoma Often involves skin, CNS, lymph nodes, lung, testes, muscles, and GI tract
  15. 15.  “low grade” lymphomas – rare in children     Follicular marginal zone/MALT primary CNS (often seen with HIV infection) peripheral cutaneous (mycosis fungoides)
  16. 16. Clinical Presentations Abdomen: (35%): pain, distention, jaundice, GI problems, mass Head/neck (13%): lymphadenopathy, jaw swelling, single enlarged tonsil, nasal obstruction, rhinorrhea, cranial nerve palsies Mediastinum (26%): SVC syndrome CNS (rare): HA, V, irritability, papilledema +Fever, malaise, night sweats, wt. loss,
  17. 17. Prognosis affected by… Incomplete remission in first 2 mos. Rx Large tumor burden (LDH >1000) Stages III and IV: CNS or BM involvement Delay in treatment Relapse **More favorable: Stage I or II, head/neck, peripheral nodes, GI tract
  18. 18. NHL Treatment Surgery for diagnostic bx or second look Radiation Therapy: emergency airway obstruction or CNS complication – may be used for local control of residual mass Chemotherapy: Combination chemo is usual, with overall cure rates 60-80+%; high risk of tumor lysis and hyperuricemia Relapse: Re-induction, followed by BMT
  19. 19. Hodgkin’s Disease Immune system malignancy, involving B or T lymphocytes Reed-Sternberg cells Spread: slow, predictable, with extension to contiguous lymph nodes Infiltration to non-lymphoid organs is rare
  20. 20. Hodgkin’s disease with Reed Sternberg cell often CD20+
  21. 21. Incidence and Etiology Hodgkin’s 5% of childhood cancers Bimodal peaks, at 15-35 and >50; rare < 5 M:F ratio of 3:1; variation r/t geography and SES, and type Increased in immunologic disorders, HIV, EBV
  22. 22. Types of Hodgkin’s Lymphoma Nodular sclerosing (NS), 40-60%, lower cervical, supraclavicular, mediastinal nodes Mixed cellularity (MC), 15-30%; advanced disease with extranodal involvement Lymphocyte predominance (LP), 5-15%, presents as localized disease Lymphocyte depletion (LD) (<5%); widespread disease
  23. 23. Clinical Presentation Painless lymph node swelling (90%) that persists despite antibiotic therapy Palpable non-tender, firm, mobile, rubbery nodes; Mediastinal adenopathy (60%); SVC Bulky: when mass is > 1/3 thorax diameter B symptoms: Fever of >38C for 3 days, drenching night sweats, 10% weight loss
  24. 24. Mediastinal masses     Risk for anesthesia (esp. if tracheal compression > 50% by CT) Least invasive diagnostic procedure therefore indicated (incl. thoracentesis) Emergent steroids or RT generally acceptable prior to biopsy HD and DLBCL tend to have areas of necrosis and therefore look more “bumpy” than T-ALL
  25. 25. Prognosis FAVORABLE: <10, F, favorable subtypes (LP and NS) and Stage I non-bulky disease UNFAVORABLE: Persistently elevated ESR; LD histopathology; bulky disease--largest dimension >10cm; B symptoms;
  26. 26. Treatment and Prognosis Dependent on age, stage, and tumor burden RT alone, CTX alone RT: varies from involved field for localized disease to extended field to total nodal irradiation, inverted Y plus mantle most often multimodal therapy, with lowdose involved field RT and multi-agent CTX Combined modality 70-90% LT cure
  27. 27. Hodgkin Px and Rx   Splenectomy generally no longer used Exact type and ratio of combined modality therapy changes… due to differences in success rates for salvage therapy and concerns for late effects of therapy   Second malignancy risks Sterility risks
  28. 28. From ABP Certifying Exam Content Outline   Know how to evaluate a child with an acute cervical lymphadenopathy Know the differential diagnosis of neck masses:     lymphoma, cystic hygroma, thyroglossal duct cyst branchial cleft abnormalities
  29. 29. From ABP Certifying Exam Content Outline, continued     Recognize the need for evaluation of supraclavicular lymph node enlargement Identify the chest x-ray as an important part of the initial evaluation of the patient with an unexplained lymphadenopathy Know that overwhelming sepsis is a serious complication in patients with Hodgkin disease who have undergone splenectomy, and know that such patients should be evaluated thoroughly if fever develops
  30. 30. Credits  Meghen Browning MD Anne Warwick MD MPH