Page 900 - Robbins Basic Pathology by Vinay Kumar, Abul K. Abbas, Jon C. Aster
P. 900
886 Index Hepatitis, viral
clinical features and outcomes for 614t, 619–620
Hemolytic anemia hepatitis A virus and 614
glucose-6-phosphate dehydrogenase deficiency as hepatitis B virus and 614
416–417 hepatitis C virus and 617–618
hereditary spherocytosis as 410–411 hepatitis D virus and 618–619
immunohemolytic anemias as 417–418 hepatitis E virus and 619
malaria as 418–419 summary for 620b
mechanical trauma and 418
paroxysmal nocturnal hemoglobinuria as 417 Hepatitis A virus (HAV) 614–620, 615f
red blood cell disorders and 408t, 409–419 Hepatitis B virus (HBV)
sickle cell anemia as 411–413
summary for 419b clinical course of 616, 616f
thalassemia as 413–416 epidemiology and transmission of 615
liver disease and 614–616, 615f
Hemolytic anemia, chronic 411–412 morphology of 617b, 617f
Hemolytic disease, in newborn 254 structure and genome of 615–616
Hemolytic uremic syndrome (HUS) viral oncogenesis and 203
in the adult 541 summary for 203b
in childhood 540–541 Hepatitis C virus (HCV)
factor H and 51
summary for 456 liver disease and 617–618, 617f
thrombotic microangiopathies and 453–454 clinical course of 618, 618f
Hemophilia A-factor VIII deficiency 455
summary for 456 morphology of 613f, 618b
Hemophilia B-factor IX deficiency 455–456 viral oncogenesis and 203
Hemorrhage
anemia of blood loss as 409 summary for 203b
introduction to 78–79, 79f Hepatitis D virus (HDV) 618–619
pulmonary diseases of vascular origin and Hepatitis E virus (HEV) 619
Hepatocellular carcinoma (HCC)
482–483
vitamin C and 301 clinical features of 639
Hemorrhage, germinal matrix 249 epidemiology of 637–638
Hemorrhage, intraventricular matrix morphology of 638b–639b, 638f
premature infants and 249 pathogenesis of 638b
preterm birth complications and 251 precursor lesions of
Hemorrhage, subarachnoid 817–819
Hemorrhoid cellular dysplasia as 636–637, 637f
clinical features of 576 dysplastic nodules as 637, 637f
morphology of 576b introduction to 636–637
as vascular disorders of bowel 576 summary for 639b
Hemosiderosis 24 Hepatocyte ballooning 621
Hemostasis, normal Hepatopulmonary syndrome 610
coagulation cascade and 83–86 Hepatorenal syndrome 610
endothelium and 79–80 Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu
hemodynamic disorders and 79–86, 80f disease) 358
platelets and 81–82 Hereditary nonpolyposis colorectal cancer (HNPCC)
Hemothorax 511 syndrome 196–197, 596, 596t, 600
Hepatic adenoma Hereditary spherocytosis
liver tumors and 636, 636f clinical features of 411
oral contraceptives and 284 hemolytic anemias and 410–411
Hepatic artery inflow 632 morphology of 410b, 411f
Hepatic encephalopathy 606–607, 835 pathogenesis of 410b, 410f
Hepatic failure summary for 419
clinical features of 604–605 Heredity
liver disease and 604–605 autosomal dominant cancer syndromes and
Hepatic nodules. See Tumor 171–172
Hepatic vein outflow obstruction autosomal recessive syndromes and 172
hepatic vein thrombosis as 634 familial cancers and 172
sinusoidal obstruction syndrome as 634 forms of cancer and 171–172, 172t
Hepatic vein thrombosis 634 Herniation 813–814, 813f–814f
morphology of 634b, 634f summary of 814b
Hepatitis, acute and chronic Heroin 285–286
liver disease and 611–621 Herpes simplex virus (HSV) 552, 560f. See also Genital herpes
morphology of 611b–614b, 612f–613f, 613t simplex
Hepatitis, autoimmune 620–621 liver disease and 620
morphology of 621b Herpesvirus
Hepatitis, chronic 619–620 morphology of 827b–828b, 827f
Hepatitis, drug/toxin-mediated injury mimicking 621 nervous system infections and 827–828
Hepatitis, fulminant 619 Heterogeneity, genetic 218–219
Hepatitis, lobular 611b–614b, 613f Heterotopia 257
High-grade squamous intraepithelial lesion (HSIL) 686,
686t
High-molecular-weight kininogen (HMWK) 52
