Page 384 - Textbook of Pathology, 6th Edition
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             TABLE 14.8:  WHO Classification of Lymphoid Malignancies (1999).
               Hodgkin’s Disease            B Cell Malignancies                  T Cell Malignancies
           Nodular lymphocytic predominant HD  Precursor (Immature) B-cell malignancies  Precursor (Immature) T-cell malignancies
           Classic HD                       Precursor B lymphoblastic leukaemia/  Precursor T lymphoblastic lymphoma/
             1. Nodular sclerosis HD        lymphoma (precursor B-cell ALL)      leukaemia (Precursor T-cell ALL)
             2. Lymphocytic rich classic HD  Peripheral (Mature) B-cell malignancies  Peripheral (Mature) T-cell and NK-cell
             3. Mixed cellularity            1. B-cell CLL/SLL (chronic lymphocytic  malignancies
             4. Lymphocytic depletion HD
                                                leukaemia/small lymphocytic lymphoma)  1. T-cell prolymphocytic leukaemia
                                             2. B-cell prolymphocytic leukaemia    2. T-cell granular lymphocytic leukaemia
                                             3. Lymphoplasmacytic lymphoma         3. Aggressive NK cell leukaemia
                                             4. Splenic marginal zone B-cell lymphoma  4. Adult T-cell lymphoma/leukaemia
                                             5. Hairy cell leukaemia                 (HTLV-I +)
                                             6. Plasma cell myeloma/plasmacytoma   5. Extranodal NK/T-cell lymphoma, nasal
                                             7. Extranodal marginal zone B-cell      type
                                                lymphoma, MALT type                6. Enteropathy-type T-cell lymphoma
                                             8. Mantle cell lymphoma               7. Hepatosplenic T-cell lymphoma
                                             9. Follicular lymphoma                8. Subcutaneous panniculitis like T-cell
                                                                                     lymphoma
                                            10. Nodal marginal zone B-cell lymphoma
                                                (Monocytoid B-cell lymphoma)       9. Mycosis fungoides/Sézary syndrome
     SECTION II
                                            11. Diffuse large B-cell lymphoma     10. Anaplastic large T lymphoma, primary
                                            12. Burkitt’s lymphoma/Burkitt cell leukaemia  cutaneous type
                                                                                  11. Peripheral T-cell lymphoma, not otherwise
                                                                                     specified
                                                                                  12. Angioimmunoblastic T-cell lymphoma
                                                                                  13. Anaplastic large T-cell lymphoma (ALCL),
                                                                                     primary systemic type




              As per WHO classification scheme  (Table 14.8), all  Relative frequency of subtypes within various NHLs listed
           lymphoid neoplasms (i.e. lymphoid leukaemias and    in Table 14.8 is as under:
           lymphomas) fall into following 5 categories:        i) Diffuse large B cell lymphoma = 31%
           I. Hodgkin’s disease                                ii) Follicular lymphoma = 22%
           II. Precursor (Immature) B-cell malignancies        iii) MALT lymphoma = 8%
           III. Peripheral (Mature) B-cell malignancies        iv) Mature T cell lymphoma = 8%
           IV. Precursor (Immature) T-cell malignancies        v) Small lymphocytic lymphoma (SLL) = 7%
           V. Peripheral (Mature) T-cell and NK–cell malignancies  vi) Mantle cell lymphoma = 6%
              Thus, in the WHO classification of lymphoid neoplasms,  vii)Mediastinal large B cell lymphoma = 2.5%
           Hodgkin’s disease stands distinctive; remaining four  viii) Anaplastic large cell lymphoma (ALCL) = 2.5%
           categories listed above fall into 2 groups:         ix) Burkitt’s lymphoma = 2.5%
                                                               x) Others = ~10%
           1) Precursor or immature lymphoid malignancies of B or T
           cell origin, meaning blastic type of leukaemias-lymphomas  2. Incidence of B, T, NK cell malignancies:  Majority of
     Haematology and Lymphoreticular Tissues
           (mainly B or T-cell ALL); and                       lymphoid malignancies are of B cell origin (75% of lymphoid
                                                               leukaemias and 90% of lymphomas) while remaining are T
           2) Peripheral or mature malignancies of B or T cell origin  cell malignancies; NK-cell lymphomas-leukaemias are rare.
           (meaning CLL and other lymphomas).
                                                               3. Diagnosis: The diagnosis of lymphoma (both Hodgkin’s
                                                               and non-Hodgkin’s) can only be reliably made on exami-
           GENERAL COMMENTS ON LYMPHOID MALIGNANCIES
                                                               nation of lymph node biopsy. While the initial diagnosis of
           Before plunging into discussion of various common examples  ALL and CLL can be made on CBC examination, bone
           in the WHO classification system, a few general aspects on  marrow biopsy is done for genetic and immunologic studies.
           lymphoid neoplasms need to be understood:           Subsequently, clinical chemistry, electrophoresis and tests
                                                               for organ involvement including CSF examination if CNS
           1.  Overall frequency:  Five major forms of lymphoid  involvement is suspected, need to be carried out.
           malignancies and their relative frequency are as under:
           i) NHL=  62%, most common lymphoma                  4. Staging:  In both HD and NHL, Ann Arbor staging is done
           ii) HD=  8%                                         for proper evaluation and planning treatment.
           iii) Plasma cell disorders = 15%                    5. Ancillary studies: CT scan, PET scan and gallium scan
           iv) CLL= 9%, most common lymphoid leukaemia         are additional imaging modalities which can be used in
           v) ALL= 4%                                          staging HD and NHL cases.
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