Page 263 - Clinical Hematology Atlas
P. 263
INDEX 247
Endoplasmic reticulum, 15f, 16f, 17-18t Erythrocytes (Continued)
Endothelial cells, 214f pallor zone of, 96f, 101
Envelope, nuclear, 17-18t peripheral smear examination, 5-10
Enzyme deficiencies, erythrocyte, 116 polychromatic, 28f, 29, 32f
Eosin pronormoblast sequence, 20f, 21, 32f
peripheral blood smears, 2-5 shape and distribution of, 97-110
in staining blood smears, 5 acanthocyte, 98
Eosinophieosinophilic bands, 74f, 75, 78f autoagglutination and, 109
Eosinophilia, 171, 174 echinocyte, 100
Eosinophilic metamyelocytes, 72f, 73, 78f elliptocyte/ovalocyte, 106
Eosinophilic myelocytes, 70f, 71, 78f hemoglobin C crystals, 104
Eosinophils, 8t, 76f, 77, 78f hemoglobin SC crystals, 105
Alder-Reilly anomaly, 211f rouleaux and, 109
in chart of hematopoiesis, 13f schistocyte, 99
maturation, 69-78 sickle cell, 103
eosinophieosinophilic band in, 74f, 75, 78f spherocyte, 101
eosinophilic metamyelocyte in, 72f, 73, 78f stomatocyte, 108
eosinophilic myelocyte in, 70f, 71, 78f target cell, 102
eosinophils in, 76f, 77, 78f size and color of, 93
in serous body fluids, 233f splenectomy and, 98, 112, 114
serous fluids with, 233f tear drop cell, 107
Erythrocytes Erythroid maturation, 19-32
in anemia, 7-10 basophilic normoblast in, 22f, 23
anisocytosis, 95 mature erythrocyte in, 30f, 31, 32f
artifact, 216-217 orthochromic normoblast in, 26f, 27
in burns, 99, 101 polychromatic erythryocyte in, 28f, 29
in chart of hematopoiesis, 13f polychromatic normoblast in, 24f, 25
cytocentrifuge slide for, 224-225 pronormoblast in, 20f, 21
dichromic populations of, 96f Erythroleukemia, 160-161
dimorphic, 95, 179, 179f Erythrophages, 229
diseases affecting, 119-134 Erythrophagocytosis, 215f
aplastic anemia, 126 Essential thrombocythemia (ET), 168, 175
b-thalassemia major, 122 Ethylenediaminetetraacetic acid (EDTA) anticoagulated
b-thalassemia minor, 121 blood, 2, 10
hemoglobin CC disease, 132 Euchromatin, 15f
hemoglobin SC disease, 134 Examination, peripheral smear, 5-10
hemoglobin SS disease, 133
hemolytic disease of the fetus and newborn, 128 F
hereditary elliptocytosis, 130
hereditary spherocytosis, 129 FAB classification. See French-American-British
immune hemolytic anemia, 127 classification
macrocytosis, 124 Fat/adipose cell, 213-215
megaloblastic anemia, 125 Fat cells, 213-215
microangiopathic hemolytic anemia, 131 Filter paper
microcytic/hypochromic anemia, 120 cytocentrifugation with, 224-225
a-thalassemia, 122 fiber artifact from, 244
distribution width, 95, 220 Flame cell, 193f
dyserythropoiesis and, 179 Folate deficiency, 94, 95, 125
enzyme deficiencies, 116 Foreign matter, 233
erythrophagocytosis of, 215f French-American-British classification
inclusions, 111-118 acute megakaryocytic leukemia, 162
basophilic stippling, 113, 117t acute myeloid leukemia, 147
cabot rings, 115, 117t acute myeloid leukemia abnormal marrow eosinophils,
Howell-Jolly bodies, 112, 117t 154-155
Pappenheimer bodies, 114, 117t acute myeloid leukemia with maturation, 150-151
with supravital stain, 116, 117t acute myeloid leukemia without maturation,
lead poisoning in, 94, 96 148-149
maturation, 30f, 31, 32f acute myelomonocytic leukemia, 154-155
mild hyperplasia, 175 erythroleukemia, 160-161
newborn normal peripheral blood morphology, 219-222 pure erythroid leukemia, 161
normochromic, 96f Fungal infection, 206
nucleated, 7-10 Fungal meningitis, 226
