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بسم الله الرحمن الرحيم
HODGKIN LYMPHOMA
EPIDEMIOLOGY H L IS common  lymphoid  malignancy  of   young Hodgkin l ymphoma r epresent  about   11%  of all lymphoma Incidence  of  HL   is    3.2   per     100.000 :1
Sex;- HL affects  males  slightly  more  than  female     1.3 ; 1 Age group;- bimodal peak      25—30     &      over   55 Associated  with        EBV      &         HIV 1st  degree relatives  of  PTS   have  5  fold  increase  in   risk
HISTOLOGY Hall  mark  is  Reed Sternberg  cell   [binucleate  CD  15 – CD30 Derived  from monoclonal population of B CELL HL  is classified in  to two main  categories   and   sub types
1—Classical  HL 2-Nodular lymphocyte predominance
Characteristic differint  CHL   &NLPHL Classical  HL     NLPHL 1-Reed  stern  berg        cell                            CD15   +      CD30 +        CD20  + _      CD45 _ EMA  _ EBV + in 50% 1-Lymphocytic   &histiocytic  cell  CD15  _      CD30 _ CD20 +      CD 45 + EMA +    EBV _
Classical H L has four sub types;- ,[object Object],Young adults.  Frequent  mediastinal  involvement  & peripheral nodes  Nodular  growth  with  fibrous bands ,[object Object],Numerous  R S & in flammatory back  ground   . associated  with  EBV & HIV ,[object Object]
Can be  associated  with  HIV  poor   prognosis,[object Object]
          clinical presenton Cervical  lymphadenopathy;-  more common  presention  about  80%  of the  Cases  [pain less  palpable cervical  masses ] Although  any  group  of lymph nodes can  be  affected Mediastinal  disease ;-  about  50%  of  the  cases, appears  as  opecity in cxray Or  as symptoms  of  compression  [repiratory  difficulty ] B symptoms ;-   fever  temp of  38 c  or higher  for  multiple  reading Un  explainded  weight  loss  more  than  10% over  6  months  .drenching
 night  sweats Usally  patients  with B symptoms  have  worse  prognosis  other  commonly   observed  symptoms;-pel-Ebstein fever --  alcohol  induced  Pain ---  bone  pain   ----abd  pain     --- neuro  pain Signs ;-hepatosplenomagaly   ---  present  of  effusions  ---  evidence  of  neuotherapys Signs  of  obs-  [extremity  edema  ----superior  vena  cava   syndrome   ---spinal  Cord  compression   lymph  nodes   examination  ;- sub mental – supraclavicular  --infrsclavicular  - Epitrochlear   --iliac  --- femoral   ---&politeal Tonsil &oropharynx ;-    waldeyer  ring  involvement  mandate  comp lety evaluation Of  NPH  …OPH   &hypopharynx by  endoscopy
                      work up After take  we  complete  H& P Lab-tests;-CBC with  differential  --- LFTS    ----BUN  --Cr     --ESR Chemistries;- alkaline phosphatase--  LDH   ---Alumen  --pregnance Test  ---HIV [ risk ] Pathologyp-   excisional  LN s biopsy       ;- mandatry  to   diagnosis  & to start  of  treatment Bone  marrow biopsy ;-inducated in  Bsymptoms --- bulky disease –stage   3-4   & Recurrent  disease
Imaging studies ;- chest  xray  PA   & LAT CT scan ;-thorax --- abd  ---&  plevis  for  staging    &  evauation  of  the  bulk Of  the  disease  and  determining  the  extent  of   the radiation  treatment CT scan  in the  neck  area  in  the  cervical   &  mediastinal  disease  ==M M W Divided  by  M TD = or  greater  than  1|3 on  BA cxray.  [GHSG]   . M M  greater Than  1o cm  in standford . Bone  scan  ;- for patients  of  high   alkaline  phosphatase  or  c bone Pain PET scan ;- is  used to evaluate  equivocal   disease seen  in  CT , to differentiating Active  versus   uninvolved  nodes   [ accuracy 95% ] Oophoropexy;-  for  women  to  preserve  ovarian  function Dental  evaluation if go to treat  the  neck Pretreatment   dental  for  neck  treatment . Staging  laprotomyno  longer  being do
                       staging Involvement  of  single  lymphatic  site;-nodal  region, waldeyer  ring Thymus  --spleen     or single  extralymphatic  organ Involvement  of  2   or  more  lymph  node region  on  the  same  side  of   the Diaphragm  or extralymphatic  organ  or  site in  association  with  regional LNs  on the same  side of the  diaphragm Involvement of  LNs  regions  of  both  side  of  the  diaphragm  which  also Associated  with extralymphatic  extension  in  aassociation  with  adjacent Lymph nodes or  spleen
Diffuse  involvement   of  one  or  more  extralymphatic  organs with  or  with  out Assciated  LNs  involvement  or  isolated  rxtralymphatic  organ  involvement In  the  absence  of  LNs  involvement   but  in  conjection  with  disease  in  distant Sites  [any  involvement  of  the  liver –bone  marrow  -lunge  -cerebrospinal Bsymptoms ;-fever ----   wt  loss   ---night  sweat  x= Bulky  disease
                     prognosis Staging;- the  most  important prognosis  factors . H L  divided  in  to  two ; - 1] early  stage;- treated  with  chemo-RT  , 5yrs  f ff  95 %   &  O S  more Than  95 %  [inculed  stage  1 &2 ] adverse  factors  inculed ESR  more Than  50  - more nodal  sites    -- bulky  mediastinal  mass  more  than 33 % of  thoracic  diameter   or  more  than  10  cms  --extranodalsites 2]Advanced  stage ;- poor  prognostic  factors  inculed male gender  --age  More  than  45 yrs   ---stage 4     --HGB  more  than  10,5  --  WBC  more Than  15   ---lymphocyte  less  than 0,6 x 10  --  albumin  less  than  40 g -- * Less than  3 factors 5 yrs f fp 70 % .  More  than  3 factors is  50 %
 B symptoms   in  all  stage  present  of  B symptoms  is  poorer   Prognosis Histopathology ;- is  independent  prognosic  variable  [ apart From  stage ]  is  less  clearly  defined  than  past  Independent  adverse  prognostic  factor  for  NSHL Include   eosinophilia   --  lymphocyte depletion   -- RS cell
                    treatment Chemo agents ;- MOPP ;-mechlorethamine  , oncovin  , procarbazine prednisone    .  ABVD ;- Adriamycin ,  bleomycin  , vinblastine  , dacarbazine BEACOPP ;-  bleomycin  , etoposide  , adriamycin  , cyclophosphamide Oncovin  , prednisone  , procarbazine Standfor v ;-mechlorethamine  , vincristine  , prednisone  , doxorubicin Bleomycin  , vinblastine  ,  etoposide .
Treatment  recommendation Stage  1A  &  2 A [ favorable  no bulky  disease - -less than  3 sites   ESR  less  than 50 ];-  ABVD  X 4  --IFRT [30 GY  [subclinical ]  36   clinical Alternative  chemo = 8 week  standford v  &IFRT  [30 GY ]  for  lp  1  A  may  give  IFRT  30  GY  or  regional  RT alone 30 – 36 gy  . stage 1 &2 A IFRT 30  then  boost  to  36  for  residual  disease Then  PET T  if  CR  chemo –[ ABVD R , CHOP R ]  Preliminary  stage  2  data  support  Rituximab . 10 yrs  EFS S 85-90 % Unfavorable ;- ABVD  x 4—6 then  [30—36 ]GY  subclinical  36 GY  CLINICAL [ bulky  disease – more  than  3sites  or  ESR more  than  50 ] Alternative  -12  week  standford v IFRT 36  to  any  node  more  than   5 cm If  refuse  chemo  STNI  [mantle –PA –splenic  ]  or mantle  alone  . 36- 44 gy 10  Yrs  FFP  82 %  OS  90 %
Stage  3 &4  ;-  4-  ABVD  then  restage  with  PET  T   if  CR . ABVD  X2   & IFRT  20-30  GY  to  bulky  sites    optional  .  If  PR  ABVD   X  2—4C ,-6 Then  IFRT   30-36   GY   to  bulky  sites   ptional  br />Alternative   ; 12  weeks  stanford v   & IFTR  36 GY [to  any  nodes  more   than   5 cms  and  residual  PET  & sites .  Or , dose  escalated  BEACOPP   with  IFRT  30 GY   to  initial  sites  more  than  5  cm . 40  GY  to  residual   PET   & areas Yrs  ffp  stage 3  75%   stage 4  65 %  os  stage  3  80 %   stage   4   75  % 10  Yrs  ffp   85 %  os  90  %
Hodgkin  lymphoma
Hodgkin  lymphoma
Hodgkin  lymphoma
Hodgkin  lymphoma
Hodgkin  lymphoma
Hodgkin  lymphoma
Hodgkin  lymphoma

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Hodgkin lymphoma

  • 3. EPIDEMIOLOGY H L IS common lymphoid malignancy of young Hodgkin l ymphoma r epresent about 11% of all lymphoma Incidence of HL is 3.2 per 100.000 :1
  • 4. Sex;- HL affects males slightly more than female 1.3 ; 1 Age group;- bimodal peak 25—30 & over 55 Associated with EBV & HIV 1st degree relatives of PTS have 5 fold increase in risk
  • 5. HISTOLOGY Hall mark is Reed Sternberg cell [binucleate CD 15 – CD30 Derived from monoclonal population of B CELL HL is classified in to two main categories and sub types
  • 6. 1—Classical HL 2-Nodular lymphocyte predominance
  • 7. Characteristic differint CHL &NLPHL Classical HL NLPHL 1-Reed stern berg cell CD15 + CD30 + CD20 + _ CD45 _ EMA _ EBV + in 50% 1-Lymphocytic &histiocytic cell CD15 _ CD30 _ CD20 + CD 45 + EMA + EBV _
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  • 10. clinical presenton Cervical lymphadenopathy;- more common presention about 80% of the Cases [pain less palpable cervical masses ] Although any group of lymph nodes can be affected Mediastinal disease ;- about 50% of the cases, appears as opecity in cxray Or as symptoms of compression [repiratory difficulty ] B symptoms ;- fever temp of 38 c or higher for multiple reading Un explainded weight loss more than 10% over 6 months .drenching
  • 11. night sweats Usally patients with B symptoms have worse prognosis other commonly observed symptoms;-pel-Ebstein fever -- alcohol induced Pain --- bone pain ----abd pain --- neuro pain Signs ;-hepatosplenomagaly --- present of effusions --- evidence of neuotherapys Signs of obs- [extremity edema ----superior vena cava syndrome ---spinal Cord compression lymph nodes examination ;- sub mental – supraclavicular --infrsclavicular - Epitrochlear --iliac --- femoral ---&politeal Tonsil &oropharynx ;- waldeyer ring involvement mandate comp lety evaluation Of NPH …OPH &hypopharynx by endoscopy
  • 12. work up After take we complete H& P Lab-tests;-CBC with differential --- LFTS ----BUN --Cr --ESR Chemistries;- alkaline phosphatase-- LDH ---Alumen --pregnance Test ---HIV [ risk ] Pathologyp- excisional LN s biopsy ;- mandatry to diagnosis & to start of treatment Bone marrow biopsy ;-inducated in Bsymptoms --- bulky disease –stage 3-4 & Recurrent disease
  • 13. Imaging studies ;- chest xray PA & LAT CT scan ;-thorax --- abd ---& plevis for staging & evauation of the bulk Of the disease and determining the extent of the radiation treatment CT scan in the neck area in the cervical & mediastinal disease ==M M W Divided by M TD = or greater than 1|3 on BA cxray. [GHSG] . M M greater Than 1o cm in standford . Bone scan ;- for patients of high alkaline phosphatase or c bone Pain PET scan ;- is used to evaluate equivocal disease seen in CT , to differentiating Active versus uninvolved nodes [ accuracy 95% ] Oophoropexy;- for women to preserve ovarian function Dental evaluation if go to treat the neck Pretreatment dental for neck treatment . Staging laprotomyno longer being do
  • 14. staging Involvement of single lymphatic site;-nodal region, waldeyer ring Thymus --spleen or single extralymphatic organ Involvement of 2 or more lymph node region on the same side of the Diaphragm or extralymphatic organ or site in association with regional LNs on the same side of the diaphragm Involvement of LNs regions of both side of the diaphragm which also Associated with extralymphatic extension in aassociation with adjacent Lymph nodes or spleen
  • 15. Diffuse involvement of one or more extralymphatic organs with or with out Assciated LNs involvement or isolated rxtralymphatic organ involvement In the absence of LNs involvement but in conjection with disease in distant Sites [any involvement of the liver –bone marrow -lunge -cerebrospinal Bsymptoms ;-fever ---- wt loss ---night sweat x= Bulky disease
  • 16. prognosis Staging;- the most important prognosis factors . H L divided in to two ; - 1] early stage;- treated with chemo-RT , 5yrs f ff 95 % & O S more Than 95 % [inculed stage 1 &2 ] adverse factors inculed ESR more Than 50 - more nodal sites -- bulky mediastinal mass more than 33 % of thoracic diameter or more than 10 cms --extranodalsites 2]Advanced stage ;- poor prognostic factors inculed male gender --age More than 45 yrs ---stage 4 --HGB more than 10,5 -- WBC more Than 15 ---lymphocyte less than 0,6 x 10 -- albumin less than 40 g -- * Less than 3 factors 5 yrs f fp 70 % . More than 3 factors is 50 %
  • 17. B symptoms in all stage present of B symptoms is poorer Prognosis Histopathology ;- is independent prognosic variable [ apart From stage ] is less clearly defined than past Independent adverse prognostic factor for NSHL Include eosinophilia -- lymphocyte depletion -- RS cell
  • 18. treatment Chemo agents ;- MOPP ;-mechlorethamine , oncovin , procarbazine prednisone . ABVD ;- Adriamycin , bleomycin , vinblastine , dacarbazine BEACOPP ;- bleomycin , etoposide , adriamycin , cyclophosphamide Oncovin , prednisone , procarbazine Standfor v ;-mechlorethamine , vincristine , prednisone , doxorubicin Bleomycin , vinblastine , etoposide .
  • 19. Treatment recommendation Stage 1A & 2 A [ favorable no bulky disease - -less than 3 sites ESR less than 50 ];- ABVD X 4 --IFRT [30 GY [subclinical ] 36 clinical Alternative chemo = 8 week standford v &IFRT [30 GY ] for lp 1 A may give IFRT 30 GY or regional RT alone 30 – 36 gy . stage 1 &2 A IFRT 30 then boost to 36 for residual disease Then PET T if CR chemo –[ ABVD R , CHOP R ] Preliminary stage 2 data support Rituximab . 10 yrs EFS S 85-90 % Unfavorable ;- ABVD x 4—6 then [30—36 ]GY subclinical 36 GY CLINICAL [ bulky disease – more than 3sites or ESR more than 50 ] Alternative -12 week standford v IFRT 36 to any node more than 5 cm If refuse chemo STNI [mantle –PA –splenic ] or mantle alone . 36- 44 gy 10 Yrs FFP 82 % OS 90 %
  • 20. Stage 3 &4 ;- 4- ABVD then restage with PET T if CR . ABVD X2 & IFRT 20-30 GY to bulky sites optional . If PR ABVD X 2—4C ,-6 Then IFRT 30-36 GY to bulky sites ptional br />Alternative ; 12 weeks stanford v & IFTR 36 GY [to any nodes more than 5 cms and residual PET & sites . Or , dose escalated BEACOPP with IFRT 30 GY to initial sites more than 5 cm . 40 GY to residual PET & areas Yrs ffp stage 3 75% stage 4 65 % os stage 3 80 % stage 4 75 % 10 Yrs ffp 85 % os 90 %