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Color Atlas of Hematology - Practical Microscopic and Clinical ...

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152Erythrocyte <strong>and</strong> Thrombocyte AbnormalitiesHyperchromic AnemiasIn patients with clear signs <strong>of</strong> anemia, e.g., a “sickly pallor,” atrophic lingualmucosa, <strong>and</strong> sometimes also neurological signs <strong>of</strong> bathyanesthesia(loss <strong>of</strong> deep sensibility), even just a cursory examination <strong>of</strong> the bloodsmear may indicate the diagnosis. Marked poikilocytosis <strong>and</strong> anisocytosisare seen, <strong>and</strong> the large size <strong>of</strong> the erythrocytes is particularly conspicuousin comparison with the lymphocytes, whose diameter they exceed (megalocytes).These are the hallmarks <strong>of</strong> macrocytic, <strong>and</strong>, with respect to bonemarrow cells, usually also megaloblastic anemia, with a mean cell diametergreater than 8 µm <strong>and</strong> a cell volume (MCV) usually greater than100 µm 3 . Mean cell Hb content (MCH) is more than 36 pg (1.99 fmol) <strong>and</strong>thus indicates hyperchromic anemia.Only when there is severe pre-existing concomitant iron deficiency is acombination <strong>of</strong> macrocytic cells <strong>and</strong> hypochromic MCH possible (“dimorphicanemia”).Table 26Most common causes <strong>of</strong> hyperchromic anemiasVitamin-B 12 deficiencyNutritional deficits, e. g.– Goat milk– Vegetarian diet– AlcoholismImpaired absorption– Genuine pernicious anemia– Status after gastrectomy– Ileum resection– Crohn disease– Celiac disease, sprue (psilosis)– Intestinal diverticulosis– Insufficiency <strong>of</strong> the exocrine pancreas– Fish tapewormFolic acid deficiencyNutritional deficits– Chronic abuse <strong>of</strong> alcoholImpaired absorption– E.g., sprue (psilosis)Increased requirement– Pregnancy– Hemolytic anemiaInterference/antagonism– Phenylhydantoin– Cytostatic antimetabolic drugs– Trimethoprim (antibacterialcombination drug)– Oral contrazeptives– Antidepressants– AlcoholAlthough other rare causes exist (Table 26), almost all patients with hyperchromicanemia suffer from vitamin B 12 <strong>and</strong>/or folic acid deficiency.Since a deficiency <strong>of</strong> these essential metabolic building blocks suppressesDNA synthesis not only in erythropoiesis, but in the other cell series aswell, over time more or less severe pancytopenia will develop.

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