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116  /  Chapter 8  White cells: Granulocytes and monocytes


                        Phagocytosis                          leukaemia and myelodysplastic syndromes may also
                                                              be associated with defective killing of ingested

                     These defects usually arise because of a lack of
                                                              microorganisms.
                    opsonization which may be caused by congenital or
                    acquired causes of hypogammaglobulinaemia or
                    lack of complement components.                Benign  d isorders
                                                                A number of the hereditary conditions may give rise
                        Killing                               to changes in granulocyte morphology (Fig.  8.8 ).

                     This abnormality is clearly illustrated by the rare
                    X - linked or autosomal recessive chronic granuloma-      Pelger – Hu ë t  a nomaly
                    tous disease that results from abnormal leucocyte

                    oxidative metabolism. There is an abnormality    In this uncommon condition bilobed neutrophils
                    aff ecting different elements of the respiratory burst   are found in the peripheral blood. Occasional

                    oxidase or its activating mechanism. Th e  patients   unsegmented neutrophils are also seen. Inheritance
                    have recurring infections, usually bacterial but   is autosomal dominant.
                    sometimes fungal, which present in infancy or early
                    childhood in most cases.
                                                                  May – Hegglin  a nomaly
                        Other rare congenital abnormalities may also
                    result in defects of bacterial killing (e.g. myeloper-    In this rare condition the neutrophils contain

                    oxidase deficiency  and  the  Ch é diak – Higashi  syn-  basophilic inclusions of RNA (resembling D ö hle

                    drome; see below). Acute or chronic myeloid   bodies) in the cytoplasm. There is an associated










                    (a)                 (b)                  (c)                 (d)











                    (e)                 (f)                     (g)

                              Figure 8.8   Abnormal white blood cells.  (a)  Neutrophil leucocytosis: toxic changes shown by the presence of


                    red – purple granules in the band form neutrophils.  (b)  Neutrophil leucocytosis: a D ö hle body can be seen in the
                    cytoplasm of the neutrophil.  (c)  Megaloblastic anaemia: hypersegmented oversized neutrophil in peripheral

                    blood.  (d)  May – Hegglin anomaly: the neutrophils contain basophilic inclusions 2 – 5   μ m in diameter; there is an
                    associated mild thrombocytopenia with giant platelets.  (e)  Pelger – Hu ë t anomaly: coarse clumping of the
                    chromatin in  pince nez  confi guration.  (f)  Ch é diak – Higashi syndrome: bizarre giant granules in the cytoplasm of
                    a monocyte.  (g)  Alder ’ s anomaly: coarse violet granules in the cytoplasm of a neutrophil.
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