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1 MBChB V: Imaging Haematology Session 2 MJ Coetzee
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2 Table of contents Haematological malignancies –Leukaemias Acute Chronic –Myeloma –Lymphoma Thrombosis & haemostasis –Thrombocytopenia –Haemophilia –DIC
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4 Leukaemias: rough classification Myeloid (granulated cells) –Chronic (myeloproliferative conditions) e.g. Chronic myeloid leukaemia (CML) –Acute myeloid leukaemias arise suddenly, deadly e.g. acute promyelocytic leukaemia Lymphoid (lymphocyte line) –Chronic e.g. Chronic lymphocytic leukaemia Course: years –Acute lymphoblastic arise suddenly, deadly e.g. acute lymphoblastic leukaemias (ALL)
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5 Lymphoid Myeloid
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6 More mature cells: chronic leukaemias More immature cells: acute leukaemias
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7 Myeloproliferative diseases
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8 Organomegaly in a patient with a myeloproliferative disease
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9 CML Chronic Myeloid Leukaemia Peripheral blood: neutrophils with left shift & eosinophils & basophils Increase in white cell layer in centrifuged blood: “leukaemia”
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10 CML: Philadelphia chromosome t(9;22)
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11 Target of Gleevec (drug against CML): works on signal transduction The normal tyrosine kinase transmits a signal from the surface to the nucleus in a controlled manner The abn. tyrosine kinase is an ONCOGENE that stimulates the nucleus to divide Intracelllular signal transducers
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12 Polycythaemia vera polycythaemia = many cells in the blood; vera = Latin for true (unexplained) Patient of Sir William Osler in whom he first described PV
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13 Many RBCs on a blood smear Cellular biopsy in PV
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14 CT of oganomegaly Splenomegaly Bone marrow fibrosis Idiopathic myelofibrosis
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15 Essential thrombocythaemia
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16 Gangrene in essential Thrombocythaemia (abnormal platelet clumping)
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17 Acute myeloid leukaemia Different classifications FAB (French-American-British) WHO (world Health Organization) Can represent different cell lines Myeloid cells of stages of maturation Promyelocytes Erythroblasts Platelets, etc.
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18 Myeloblasts: peripheral blood
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19 Myeloblasts with an Auer rod
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20 AML Bone marrow packed with blasts Myeloblasts with granules (granules are typical of myeloid cells
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21 Lymphoid leukaemias Chronic lymphocytic leukaemia Acute lymphoblastic leukaemia
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22 CLL (chronic lymphocytic leukaemia): clinically Cervical lymph nodes Mediastinal lymph nodes
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23 CLL bone marrow: infiltrates of mature lymphocytes
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24 CLL: peripheral blood with many lymphocytes
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25 CLL: laboratory CLL cells express typical antigens op their membranes. These are detected by means of flow cytometry
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26 ALL: clinical picture Rapid course Lymphadenopathy Organomegaly Haemorrhages Infections
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27 ALL: lymphoblasts
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28 Burkitt's lymphoma/leukaemia blasts
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29 Myeloma Vague complaints –Bone pain –Fractures –Infections –Malaise Please remember to determine paraproteins in blood and urine 1% of cancers > 10 % of haematologic cancers in the US Annual incidence ± 4 per 100,000 Increase in cases –?enhanced availability and use of medical facilities
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30 Monoclonal band of abnormal Ig Normal Myeloma Normal
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31 Myeloma Osteopenia Lytic lesions Pathological fractures
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32 Myeloma: rouleaux on peripheral blood
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33 Myeloma: plasma cells in bone marrow
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34 Congested veins resulting from paraproteins, esp. IgM
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35 Haemostasis Haemorrhagic diatheses –Hereditary haemorrhagic diatheses Haemophilia Von Willebrand disease –Acquired haemorrhagic diatheses ITP Thromboses –Venous –Arterial
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36 Purpura (fine peticchiae)
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37 Purpura (ecchymoses): larger bleeds
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38 Haemarthrosis in haemophilia
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39 Haemophilia: X-rays (ankylosis) Knee Elbow
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40 Haemophilia Family tree
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41 Haemophilia: repeated bleeds Dark hypertrophic synovium; osteoartritis; osteophytes
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42 Dangerous bleeds Bleed in floor of the mouth stretches downward and obstructs the airways Volkman contracture or compartment syndrome of fore arm (hand useless)
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43 ITP: bone marrow packed with megakaryocytes
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44 TTP: few platelets red cell fragments (always exclude HIV)
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45 Superficial thromboses: clinically Skin necrosis
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46 DIC: clinical picture
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47 DIC: histological picture
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