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12  Haematology  351


             •  Infections
               •  Viral: HSV, rubella, smallpox, hepatitis, CMV and epidemic haemorrhagic fever
               •  Bacterial: Meningococcaemia and septicaemia (Gram-positive)
               •  Mycotic: Histoplasmosis and aspergillosis
               •  Protozoal: Malaria, kala-azar and trypanosomiasis
               •  Metazoal: Heartworm disease in dogs
             •  Neoplasms: Carcinoma prostate, ovary, pancreas, breast, lung, carcinoid, rhabdomyo-
               sarcoma, neuroblastoma and acute promyelocytic leukaemia
             •  Others: PNH, incompatible transfusions, fresh water submersion and drug induced

             Laboratory Diagnosis
               1.  Acute DIC
             Clinical	findings:
               •  Multiple bleeding sites
               •  Ecchymoses of skin and mucous membranes
               •  Visceral haemorrhage
             Laboratory	abnormalities: Consumption of clotting factors and platelets and intravascular
               haemolysis:
               •  Decreased levels of Factors II, V and VIII
               •  Fibrinogen level below 1.0 g/L
               •  Increased FDP (fibrin degradation products, eg, FDP, D dimer)
               •  Platelet count below 100 3 10  /L
                                          9
               •  Prolonged thrombin time (deficiency of fibrinogen and increased FDP levels which
                 inhibit  thrombin  activity),  prolonged  prothrombin  time  (PT)  and  activated  partial
                 thromboplastin time (PTTK)
               2.  Chronic DIC
             Clinical	findings:
               •  Signs of deep venous or arterial thrombosis/embolism
               •  Superficial venous thrombosis
             Laboratory	abnormalities:
               •  Modestly increased prothrombin time in some patients
               •  Shortened or lengthened partial thromboplastin time
               •  Normal thrombin time in most patients
               •  High, normal or low fibrinogen level
               •  High, normal or low platelet count
               •  Increased levels of FDP (eg, on testing for FDP, D dimer)

             Q. What are blood groups? Enumerate the important blood group
             systems.

             Ans.  Blood groups are genetically determined antigens that can be detected on the RBC
             surface by specific antibodies (Table 12.22).





               TABLE 12.22.   Important blood group systems
               Name of blood group system  Name of antigens
               ABO                       H, A 1 , A 2  and B
               Rh                        D, C, E, c and e
               P                         P and p
               MNS                       M, N, S and s
                                           a
               Lutheran (Lu)             Lu  and Lu b
                                           a
               Lewis (Le)                Le  and Le b
                                           a
               Duffy (Fy)                Fy  and Fy b
               Kidd (JK)                 JK and JK


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