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Phagocytosis
Hodgkin’s Lymphoma
    Sarcoidosis


                     Jori Lambert
   The human body has many mechanisms
    within the immune system to protect itself
    from external and internal pathogens.

   However, when something goes wrong with
    these mechanisms, the results can be
    devastating to the cells, tissues, and organs
    of the lymphatic and immune systems.
   Nonspecific innate response to any pathogen
    that reaches the connective tissue beneath
    skin and mucosae.

   Cytoplasmic extensions reach out to engulf
    foreign matter. Used by macrophages, which
    are the “large eaters”.
   Phagocytes must correctly
    identify and bind to the
    pathogen’s membrane.

   Pathogen is then pulled
    inside and fuses with a
    vesicle containing strong
    acidic enzymes-lysosome.

   The enzymes break it down
    into harmless debris for
    the body to sweep up.
   If a pathogen resists
    digestion by lysosyme,
    helper T cells assist the
    phagocyte by activating
    stronger enzymes

   The release of free
    radicals like nitric oxide
    and hydrogen peroxide
    or protein-digesting
    enzymes occur in the
    respiratory burst.
   Lymphatic system cancer

   Abnormal cell growth that can spread to
    other systems

   Mutation happens in B cells called Reed-
    Sternberg cells, they proliferate and group
    together in the lymphatic system.

   Impaired immune response in body results in
    increased susceptibility to infection
Microscopic view of   PET scan showing affected regions
mutated B cell
   Often associated with previous Epstein-Barr
    virus infection-mononucleosis

   Immunocompromised or immunosuppressed
    patients

   Family history of lymphoma, particularly in
    siblings.
   Swelling in principal lymph
    node locations i.e. axillary,
    inguinal and cervical
    regions.

   Similar to symptoms of flu:
    lethargy or fatigue, fever
    and chills, night sweats,
    chest pain, coughing, loss      Enlarged lymph nodes in
    of appetite.                    cervical region.

   Noticeable, unexplained
    weight loss.
   Stage 1: One cancerous node or organ.
   Stage 2: Two cancerous nodes or small
    affected region.
   Stage 3: Nodes in regions above and below
    diaphragm are cancerous, or tissue near
    spleen is affected.
   Stage 4: Several organs or tissues are
    cancerous and had spread to bones, lungs,
    and other parts of body.
       NOTE: Stage 1&2 diagnosis has 80% remission rate for 5 years.
             Stage 3&4 diagnosis has less than 60% remission rate
             over same period of time.
   Physical examination, Blood tests, CT, MRI, X-
    ray, biopsy of swollen node, and bone
    marrow aspiration.

   Treatment typically is a two-step process.
    Chemotherapy is typically used first and then
    radiation therapy.

    Stem cell transplant can be used if the cancer
    returns or resists initial treatment.
   Inflammation resulting in abnormal tissue
    clumps, granulomas, in body.

   Often found in lymph nodes, lungs, liver,
    eyes, and skin.

   Unknown origin, but may be genetic,
    environmental sensitivity, or hyper immune
    response to an infection.
   Higher incidence in African American
    population.

   If blood relative has it, increases your chances
    by five times.

   Mostly begins between ages of 20 and 40.
   Most cases have chest
    symptoms such as chest
    pain, dry cough, and
    shortness of breath.
                                     Eye lesions

   Wide array of presentation
    elsewhere. Overall fatigue,
    fever, joint pain, rash,
    headaches, vision loss,
    burning in eyes, and nose
                                  Rash, skin plaques
    bleed.
   Physical exam, chest x-ray or CT often finds
    enlarged organs such as liver or spleen, and
    enlarged lymph glands.



   Biopsy of abnormal growth
   Primary therapy is corticosteroid, but length
    of treatment depends on severity of disease.

   Immunosuppresants can be used to calm an
    overactive immune system.

   Most affected see improvement, but others
    may develop tissue damage especially in
    lungs and heart that can cause death.
   Foundation for Sarcoidosis Research
    http://www.stopsarcoidosis.org/sarcoidosis/diseasefact
    s.htm?gclid=CMbJ_tmo1LICFY1DMgodK0QACQ
   Mayo Clinic:
    http://www.mayoclinic.com/health/hodgkins-
    disease/DS00186
   National Cancer Institute (National Institute of Health)
    http://www.cancer.gov/cancertopics/types/hodgkin
   US National Library of Medicine:
    http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001
    140/
   http://www.nlm.nih.gov/medlineplus/hodgkindisease.h
    tml
   http://www.peterjurek.com/rbv_site/web_pa
    ges/phagocytosis.html
   http://www.inflammation-information.com/
   http://www.cancer.gov/
   http://www.netterimages.com/image/3017.h
    tm
   http://www.medicalgeek.com

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Ch. 6present

  • 1. Phagocytosis Hodgkin’s Lymphoma Sarcoidosis Jori Lambert
  • 2. The human body has many mechanisms within the immune system to protect itself from external and internal pathogens.  However, when something goes wrong with these mechanisms, the results can be devastating to the cells, tissues, and organs of the lymphatic and immune systems.
  • 3. Nonspecific innate response to any pathogen that reaches the connective tissue beneath skin and mucosae.  Cytoplasmic extensions reach out to engulf foreign matter. Used by macrophages, which are the “large eaters”.
  • 4. Phagocytes must correctly identify and bind to the pathogen’s membrane.  Pathogen is then pulled inside and fuses with a vesicle containing strong acidic enzymes-lysosome.  The enzymes break it down into harmless debris for the body to sweep up.
  • 5. If a pathogen resists digestion by lysosyme, helper T cells assist the phagocyte by activating stronger enzymes  The release of free radicals like nitric oxide and hydrogen peroxide or protein-digesting enzymes occur in the respiratory burst.
  • 6. Lymphatic system cancer  Abnormal cell growth that can spread to other systems  Mutation happens in B cells called Reed- Sternberg cells, they proliferate and group together in the lymphatic system.  Impaired immune response in body results in increased susceptibility to infection
  • 7. Microscopic view of PET scan showing affected regions mutated B cell
  • 8. Often associated with previous Epstein-Barr virus infection-mononucleosis  Immunocompromised or immunosuppressed patients  Family history of lymphoma, particularly in siblings.
  • 9. Swelling in principal lymph node locations i.e. axillary, inguinal and cervical regions.  Similar to symptoms of flu: lethargy or fatigue, fever and chills, night sweats, chest pain, coughing, loss Enlarged lymph nodes in of appetite. cervical region.  Noticeable, unexplained weight loss.
  • 10. Stage 1: One cancerous node or organ.  Stage 2: Two cancerous nodes or small affected region.  Stage 3: Nodes in regions above and below diaphragm are cancerous, or tissue near spleen is affected.  Stage 4: Several organs or tissues are cancerous and had spread to bones, lungs, and other parts of body. NOTE: Stage 1&2 diagnosis has 80% remission rate for 5 years. Stage 3&4 diagnosis has less than 60% remission rate over same period of time.
  • 11.
  • 12. Physical examination, Blood tests, CT, MRI, X- ray, biopsy of swollen node, and bone marrow aspiration.  Treatment typically is a two-step process. Chemotherapy is typically used first and then radiation therapy.  Stem cell transplant can be used if the cancer returns or resists initial treatment.
  • 13. Inflammation resulting in abnormal tissue clumps, granulomas, in body.  Often found in lymph nodes, lungs, liver, eyes, and skin.  Unknown origin, but may be genetic, environmental sensitivity, or hyper immune response to an infection.
  • 14.
  • 15. Higher incidence in African American population.  If blood relative has it, increases your chances by five times.  Mostly begins between ages of 20 and 40.
  • 16. Most cases have chest symptoms such as chest pain, dry cough, and shortness of breath. Eye lesions  Wide array of presentation elsewhere. Overall fatigue, fever, joint pain, rash, headaches, vision loss, burning in eyes, and nose Rash, skin plaques bleed.
  • 17. Physical exam, chest x-ray or CT often finds enlarged organs such as liver or spleen, and enlarged lymph glands.  Biopsy of abnormal growth
  • 18. Primary therapy is corticosteroid, but length of treatment depends on severity of disease.  Immunosuppresants can be used to calm an overactive immune system.  Most affected see improvement, but others may develop tissue damage especially in lungs and heart that can cause death.
  • 19. Foundation for Sarcoidosis Research http://www.stopsarcoidosis.org/sarcoidosis/diseasefact s.htm?gclid=CMbJ_tmo1LICFY1DMgodK0QACQ  Mayo Clinic: http://www.mayoclinic.com/health/hodgkins- disease/DS00186  National Cancer Institute (National Institute of Health) http://www.cancer.gov/cancertopics/types/hodgkin  US National Library of Medicine: http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001 140/  http://www.nlm.nih.gov/medlineplus/hodgkindisease.h tml
  • 20. http://www.peterjurek.com/rbv_site/web_pa ges/phagocytosis.html  http://www.inflammation-information.com/  http://www.cancer.gov/  http://www.netterimages.com/image/3017.h tm  http://www.medicalgeek.com