Page 264 - Clinical Hematology Atlas
P. 264
248 INDEX
G Hereditary elliptocytosis, 106, 130
Hereditary ovalocytosis, 106
Gaucher disease, 210-212 Hereditary pyropoikilocytosis, 130f
Glycogen aggregates, 15f Hereditary spherocytosis, 129
Golgi body, 16f, 17-18t Hereditary stomatocytosis, 108
Golgi complex, 15f Heterochromatin, 15f
Gout, synovial crystals in Histiocyte, sea blue, 215f
calcium pyrophosphate, 239-241 Histiocytes, 66f, 67, 68f
monosodium urate, 241-243 sea blue, 215f
Graft rejection, renal, 99 Histoplasma capsulatum, 206f, 231f
Granulation, toxic, 140, 198, 199f Homozygous hemoglobin C disease, 104, 132
Granules Homozygous hemoglobin S disease, 103, 133
Alder-Reilly anomaly, 211f Howell-Jolly bodies
azurophilic, 8t, 44, 89f hemoglobin SS disease, 133
Chédiak-Higashi anomaly, 212f megaloblastic anemia, 125
mast cells, 213f in newborns, 221f
monocytes versus reactive lymphocyte, 143t staining qualities of, 112, 117t
siderotic, 114 Hyperplasia, 175
Growth factors, myeloid hemopoietic, 197-200 Hypersegmentation, 137
Hypochromia, 96f, 121, 123
H Hypogranulation/agranulation, 141
Hyposegmentation, 136
Hairy cell leukemia, 191
Head trauma, 244 Hyposplenism, 112
Heinz bodies, 116f Hypothyroidism, 98
Hematogones, 220, 221 I
Hematoidin crystals, 229, 230f
Hematological manifestations of inherited disorders, Immune hemolytic anemia, 127
210-212 Immunoglobulin staining, 193
Alder-Reilly anomaly, 211f Inclusions in erythrocytes, 111-118
Chédiak-Higashi anomaly, 212f basophilic stippling, 113, 117t
Gaucher disease, 210-212 cabot rings, 115, 117t
May-Hegglin anomaly, 211f Howell-Jolly bodies, 112, 117t
Niemann-Picke disease, 210 Pappenheimer bodies, 114, 117t
Sanfilippo syndrome, 210f with supravital stain, 116, 117t
Hematopoiesis, 12 Infections, leukocytes in
chart of, 12, 13f degranulation/agranulation, 141
Heme synthesis, 113 nuclear hyposegmentation, 136
Hemoglobin Infectious mononucleosis, 142f
Bart’s, 123f Inherited disorders, hematological manifestations of,
Heinz bodies and, 116f 210-212
Hemoglobin CC disease, 132 Alder-Reilly anomaly, 211f
Hemoglobin C crystals, 104 Chédiak-Higashi anomaly, 212f
Hemoglobin H, 116f, 122 Gaucher disease, 210-212
Hemoglobinopathies May-Hegglin anomaly, 211f
inclusions in, 114, 116 Niemann-Pick disease, 210
shape and color of, 102 Sanfilippo syndrome, 210f
size of, 94 Intracranial hemorrhage, 229
Hemoglobin SC crystals, 105 Intrathecal injections, 226
Hemoglobin SC disease, 134 Intravascular coagulation, disseminated, 99, 131
Hemoglobin SS disease, 133 Iron deficiency anemia, 120
Hemoglobinuria, 173 Iron granules, 114, 229
Hemolysis, 96 Iron stain, 114f, 181f, 229
Hemolytic anemia, 127
Hemolytic disease of the fetus and newborn, 128 L
Hemolytic hereditary elliptocytosis, 130
Hemolytic uremic syndrome, 99, 131 LAP (leukocyte alkaline phosphatase), 168, 172-173
Hemoph, 96f LE (lupus erythematosus), 233f
Hemorrhage Lead poisoning, 94, 96
central nervous system, 229-230 Leukemia
erythrocytic hemoglobin in, 96f acute erythroid, 160-161
Hemosiderin, 229f, 230 acute lymphoblastic
