Lab Diagnosis 11.1.99

 

Hemolytic anemia—condition of inadequate red cells caused by premature destruction of red cells.

·        Lysis or cell death

·        Hereditary

·        Occurs if the marrow is unable to compensate therefore it becomes clinical

·        Intrinsic—factor ionside the red cell causeng the anemia

·        Extrensic—factors outside the red cell causing the anemia

·        Classification

·        Aplastic

·        Hemoglobin SC

·        Hemolysis due to G-6-Phosphate

·        Idiopathic

·        Autoimmune—due to medications

·        Anemia can be caised by medication, poor nutrition and heredity

·        Hemolytic anemia

·        Associated with jaudice and icterus or yellowing of the eyes, skin and mucous membranes  caused by too much billirubin

·        Occurs due to breakdown of billirubin, which is broken into a heme and globin portion.

·        New born jaundice can be normal

·        All other forms of jaundice are due to liver failure and results form indirect or conjugated billirubin build up.

 

Aplastic anemia—idiopathic form

·        Absence of cell growth

·        Idiopathic—bone marrow fails to make all cell lines

·        Stem cell—progenator cell that gives rise to all cell lines leading to pancytopenia

·        Pancytopenia—is incompatible with life due to lacking in any of the cells.

·        Can be due to lupus, toxins, radiation which all attack the stem cell.

·        Can result in multi-organ failure.

·        Produces fgatigue and weakness, as well as bleeding and may be acute or chronic.

·        Also has dyspnea, tachycardia, easy brusing and bleeding gums

·        Splenomegaly which is one of the terminal signs, and sternal pain may be present—seen on CT scan.

·        ¯ counts in all cell lines

·        ­ hemolysis and ­ billirubin

·        terminal prognosis—if untreated, transplants may be successful in younger patients

·        treated with bone marrow transplant in people under 40

·        over 40, antithymocyte globulin ATG is the preferred method of choice which suppresses the immune system

 

 

Secondary aplastic anemia—identifiable cause

·        Involves stem cell injury—leading to pancytopenia

·        Chemotherapy is the leading cause and is an expected

·        Radiation and toxins (benzene) is the most common.

·        Pregnancy may also cause this as well as lupus which can injure the stem cell

·        May be acute or chronic

·        4 out 100,000 which is more common form

·        Prevention may be unavoidable

·        Splenomagaly, sternal tenderness

·        ¯ hematocrit and hemoglobin.

·        Treatment: conservative care in mild cases, as well as the same as above.

·        Prognosis—untreated leads to rapid death

 

Leukocytes

·        Types

·        Granulocytes

·        Neutrophils—most common 40-60%

·        Eosinophils—4%

·        Basophils—0-2%

·        Agranulocytes

·        Monocytes—10%

·        Lymphocytes—20-40% dominant in children under 14

·        Count is between 5-10 thousand

 

Case

·        Left shift all white cells and bands are ­ but lymphocytes are ¯àindicates bacterial infection or inflammation.

·        Lymphocytes are ¯ relative to the other cell counts

·        Bands are adolescent white cell

·        Right shift—low or low normal white cells, with normal bands, and the lymphocytes are ­à due to viral infection.

·        Bands indicate a left shift

 

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