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G-cell hyperplasia, 150, 160-62, 163
galactosemia, 67t, 521t
gallbladder: anatomy, 183; dilated, 31; in cystic fibrosis, 434t,
436;
inflamed see cholecystitis; postgastrectomy
problems, 164t, 167
gallbladder disease: acalculous cholecystitis, 454-55; cholecystoses,
455; congenital, 454; neoplasms, 456;
postcholecystectomy, 455
gallstones see cholelithiasis
gamma-glutamyl transpeptidase, 471
ganciclovir, 293t, 299
Gardner’s syndrome, 355
gas see also dyspepsia; about, 15-18; children, 567; in celiac
disease,
243t, 244; in cholelithiasis, 449; in
cholesterolosis, 455; in cystic fibrosis,
434; in diarrhea, 236; in
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diverticulosis,
356; in gastroenteritis, 228; in GERD, 108; in giardiasis,
230; in irritable bowel syndrome, 361-63, 364t;
in malassimilation,
62, 203, 206, 211; in pancreatic cancer, 426; in
pancreatitis, 419; in
parasitic infection, 376; in small bowel ischemia,
259; infants, 577;
production of, 352
gaseous distention see gas
gastrectomy, 163-67, 171, 172, 173, 175, 249
gastric acid secretion: assessment, 145-37; failure, 168-71; in PUD,
148, 150-51; inhibition, 155, 158; mechanism,
149-51
gastric atrophy, 169
gastric endocrine secretion, 145
gastric erosions, 34t
gastric folds, 163, 171t
gastric inhibitory polypeptide (GIP), 140, 144, 150
gastric rupture, 176
gastric ulcer disease: acid secretion, 150; causes, 144, 165;
pathophysiologic defects, 137, 147t; upper
GI bleeding, 34t
gastric varices, 171t
gastric volvulus, 175
gastrin: causing diarrhea, 234t, 239; role in digestion, 139-40,
405;
secretion, 139, 145, 149-51, 430-31
gastrin-receptor antagonists, 155
gastrin-releasing peptide (GRP), 145
gastrinoma, 143, 160-63, 165, 430-31
gastritis: acute, 168, 171t; atrophic, 143, 170-74; bile, 172;
causes,
144, 171, 177-81; chronic, 147t, 168-70,
172; classification,
168t; eosinophilic, 171t, 171-72;
erosive, 172; granulomatous,
171; hypertrophic, 170-71; inflammatory, 528;
lymphocytic, 171t;
Ménétrier’s disease, 170-71; metaplastic, 171;
superficial, 170;
treatment, 155
gastritis cystica profunda, 171t
gastroenteritis: clinical features, 8; eosinophilic, 112, 377-78;
infections,
224-28, 229
gastroenterostomy, 161, 249
gastroesophageal reflux disease (GERD) see GERD
gastrojejunostomy, 166
gastroparesis, 108
gastropathy: hypertrophic-hypersecretory, 171; portal hypertensive, 528-29
gastrostomy, percutaneous endoscopic, 115
gender see sex
geographical factors: cholelithiasis, 440, 441t; esophageal cancer,
125-26
GERD: children, 110, 573-77; clinical features, 5-8, 96-97, 105-6;
complications, 6, 107, 109-10, 574-75, 575t;
diagnosis, 106t, 106-8;
and esophageal disorders, 116, 119; and hiatus
hernia, 100, 103;
and LES function, 94; pathophysiology, 100, 103,
104f; postsurgical,
115, 118, 163-65, 164t; treatment, 108-9
giant cell carcinoma, 426
giant hypertrophic gastritis see Ménétrier’s disease
giant mucosal rugal hypertrophy, 170-71
Giardia lamblia: about, 230; causing diarrhea, 23t, 24, 223t,
594, 600;
HIV-associated, 293t, 296
Gilbert’s syndrome, 57t, 468, 477, 616-17
GIP see gastric inhibitory polypeptide (GIP)
globulins, 409, 464, 471-72
globus, 4-5
glomerulonephritis, 489, 499, 516, 541
glossitis: children, 590; in celiac disease, 243t; in intestinal
malassimilation,
206, 208t; in vitamin and mineral
deficiency, 25, 57, 58t-59t, 210t, 212
glucagon: causing diarrhea, 239; role in digestion, 49, 50t, 52,
144;
secreted, 400, 430; to treat esophageal
obstruction, 132
glucagonoma, 430
glucoamylase, 201
glucocorticoids, 196, 377
glucokinase, 54
gluconeogenesis, 54
glucose: in digestion, 50, 52, 192, 200-201, 464; in malnutrition, 60,
235t, 434t, 435; in starvation, 54;
replacement, 71-72
glucose galactose, 235t
glucose-6-phosphatase, 54
glucose-6-phosphate dehydrogenase, 54
beta-glucuronidase, 443, 452
glucuronyl transferase, 467
glutamine, 57
glycerin, 582
glycine, 57, 205, 250-51
glycogen, 50, 54, 464
glycogen storage disease, dietary therapy, 67t
glycogenesis, 57t, 464, 521t
glycolysis, 54
glycoproteins, 464
glypressin, 529
goiter, 9, 208t
gonococcus, 24
gonorrhea, 290, 391
graft dysfunction, 547-48
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graft-versus-host disease, 112, 128, 516, 525t, 557
granular cell tumor, esophageal, 124t, 124
granuloma, 306, 316, 517
granulomatous inflammation, liver, 510-11
Grey Turner’s sign, 414
group D streptococci, 536
“growing” pains, 566
growth failure see failure to thrive
growth hormone, 52
GRP see gastrin-releasing peptide (GRP)
guanethidine, 223t
guanylate cyclase, 238
Guillain-Barré syndrome, 489
gum disease, 58t
gut hypersensitivity, 17-18
gut transit study, 20
gynecomastia, 466t, 504-5
-H-
H+/K+-ATPase, 151, 155
H+/K+-ATPase inhibitors, 158
H+/K+-ATPase pump see hydrogen
H2 antagonists, 576
H2 blockers see H2-receptor antagonists
H2-receptor antagonists: and gastric secretions, 142-43; side effects,
157t; to treat dysphagia, 10; to treat
gastrinoma, 163; to treat gastritis,
171; to treat GERD, 107t, 108; to treat
pancreatitis, 424; to treat PUD,
155, 157-59, 165
hair problems, 56, 208t, 212
halothane, 509
hamartoma, small intestine, 259
Harris-Benedict equation, 67
head circumference, children, 571, 583-84, 585t, 589-90, 604
headache, 255, 362, 566
Health Protection Branch, Health Canada, 81-82, 85
heart disease, 255, 257, 269, 277, 280, 369, 469
heart failure, 58t, 114t, 210t, 512, 525t,
555-56
heartburn: about, 5-8, 13; and esophageal motor disorders, 116;
in achalasia, 118; in GERD, 95, 105; in
scleroderma esophagus, 119
height, children, 583-84, 585t, 589-90, 591t, 604
Helicobacter pylori, 11-12, 149t, 155, 160, 173, 177-81
HELLP syndrome, 555
hemangioma: esophageal, 124t; liver, 550-51
hematemesis see blood in vomit
hematochezia see blood in stool
hematoma, perianal, 380
hemochromatosis: cause, 57t; dietary therapy, 67t; in
cirrhosis,
520-21, 521t; in inherited liver disease,
512-13; in liver neoplasms, 551
hemoglobinuria, 556
hemolysis, 31, 209t, 443
hemophilia, 289
hemorrhage: causing ischemia, 277; colonic, 230, 280, 342; diagnosing,
3, 34; esophageal, 89; in inflammatory bowel
disease, 311t; in liver
disease, 517, 524, 553; in pancreatitis, 410-11,
413-14, 420; in PUD,
160; and vitamin deficiency, 59t
hemorrhoidectomy, 388
hemorrhoids, 35t, 41, 339t, 380-81, 385-88, 394, 396
hemosiderin, 283
hemosiderosis, 512
hepatectomy, 456
hepatitis A, 479-80, 480f, 488, 515
hepatitis, active see hepatitis, chronic
hepatitis, acute see also specific types; causes, 479t, 479,
485;
clinical features, 468-69, 485; complications,
487-90; diagnosis,
485-87; drug-induced, 509; figures, 486f-88f;
fulminant, 469, 487-88;
relapsing, 489; treatment, 490-91; types, 479-85
hepatitis, alcoholic, 57t, 303, 479t, 501, 503-4, 515t,
525t, 526
hepatitis, autoimmune, 493, 495t, 500-501
hepatitis B: about, 479-82, 491; causing cirrhosis, 505, 520, 521t;
chronic, 494-98; complications, 487, 489, 553; and
hepatorenal
syndrome, 541; HIV-associated, 302-3; illicit drug
risks, 291; and liver
neoplasms, 551; risk factors, 482t
hepatitis C: about, 479, 482-83; causing cholestasis, 515; causing
cirrhosis,
505, 520, 521t; chronic, 494, 498-500, 513;
complications, 487, 489-91;
HIV-associated, 302-3; illicit drug risks, 291;
and liver neoplasms, 551
hepatitis, chronic see also specific types; causes, 311t,
339t, 490, 511;
causing cirrhosis, 520, 521t; causing
portal hypertension, 525t; clinical
features, 467, 469, 492-94, 525t;
diagnosis, 495t; figures, 493f-94f;
typology, 492-93
hepatitis D: about, 479t, 484, 491; causing cirrhosis, 520, 521t;
chronic,
494, 500; complications, 487-90
hepatitis, drug-induced, 493, 495t, 500
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hepatitis E, 479t, 484, 552-53
hepatitis F, 484
hepatitis G, 485, 487; chronic, 494
hepatitis, ischemic, 471
hepatitis, neonatal, 513, 620
hepatitis, viral see also specific types, 492t,
494-500, 515t, 520, 521t,
523, 552
hepatitis serology, 472
hepatobiliary disease, children, 611-12
hepatobiliary function, 463-65
hepatocellular carcinoma, 57t, 497, 505, 513, 549-52
hepatocellular disease: clinical features, 31-32, 468, 469; in ulcerative
colitis, 339t, 342-43; reduces coagulation
factors, 464
hepatocellular injury, 508t, 508-9
hepatocytes, 463
hepatomegaly: diagnosing, 25, 38, 56; in bile duct disease, 460;
in congestive heart failure, 555; in esophageal
disease, 97, 126;
in hemochromatosis, 512; in hepatic vein
thrombosis, 556; in liver
disease, 466t, 468-69, 504, 505, 523; in
malassimilation, 209t;
in veno-occlusive disease, 556
hepatorenal syndrome, 505, 540t, 540-41
hepatosplenomegaly, 501, 519, 612
hepatosteatonecrosis see fatty liver
heredity: celiac disease, 242-44; cholelithiasis, 444t; Crohn’s
disease,
308t, 308; familial short stature, 586-87;
hepatitis, 500;
hyperbilirubinemia, 477-78; liver disease, 67t,
476, 512-14; neoplasms,
172, 173, 353, 355-56; pancreatitis, 418; PUD,
147-48; pyloric stenosis,
176; RAP, 566; ulcerative colitis, 308t,
308
hernia, 359
Herpes simplex: causing esophagitis, 8, 111; causing gastritis, 177;
causing hepatitis, 479t, 479;
HIV-associated, 293t, 299-300, 391;
postsurgical, 549
heterosexuality, 289
heterotopia, esophageal, 124t
hiatus hernia, 5-6, 100, 101f, 102f, 103, 175
Hill posterior gastropexy, 109
hilum, 136
Hirschsprung’s disease, 19t, 20, 348, 370-71, 581
histamine, 150
histoplasmosis, 177, 292t, 295
history-taking, 3-4
HIV: GI involvement, 288, 290-302; hepatobiliary involvement, 302-3;
HIV enteropathy, 300-301; neoplasms, 301-2;
nutrition, 304; pancreatic
involvement, 303-4; prevalence, 288; principles of
infection, 288-90
HIV wasting syndrome, 304
hoarseness, 97, 105-6, 112, 126
Hodgkin’s disease, 301
homosexuality: and diarrhea, 24; and hepatitis, 491; HIV risk, 289,
299; and infection, 290, 296, 299, 301-2, 390; and
neoplasms, 301-2
hookworms, 376
hormones see also specific types; affecting electrolyte
absorption, 196-97;
causing diarrhea, 238-39, 240, 594; and
cholelithiasis, 444t; in digestion,
49-53, 50t, 54, 400
human immunodeficiency virus see HIV
human papilloma virus, 302
hunger, 15
hydralazine, 123
hydrocephalus, 14
hydrochloric acid: in diarrhea, 236; in gastric juices, 139, 141, 151,
194f; measuring, 145-37; role, 135, 140,
150
hydrocortisone acetate, 334
hydrogen see also H+/K+-ATPase, 193-95, 194f
hydrogen sulfide, 250
hydrops, gallbladder, 452
beta-hydroxybutyrate dehydrogenase, 54
hydroxycobalamin, 169
hydroxyproline, 205
hydroxyzine, 624t
hyoscyamine, 364t
hyperalimentation, 418
hyperamylasemia, 269-70, 408-10, 409t, 414
hyperbilirubinemia: causes, 32f, 32, 616t, 619t;
congenital, 477-78;
conjugated, 618-23; diagnosing, 621f, 623f;
in cholecystitis, 450;
in congestive heart failure, 556; in liver
disease, 467-68, 504; in
malnutrition, 57t; treatment, 618, 624;
unconjugated, 615-18
hypercalcemia, 20, 160, 369, 413
hypercatabolism, 24
hyperchlorhydria, 160
hypercholesterolemia, 517
hypercoagulability, 556
hyperdynamic circulation, 466t, 467
hypergammaglobulinemia, 501
hypergastrinemia, 158, 160-63, 241t
hyperglycemia, 506
hyperimmune bovine colostrum, 231
hyperkeratosis, 59t, 210t
hyperlipidemia, 413, 502
hyperlipoproteinemia, 412
hyperoxaluria, 249
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hyperparathyroidism, 413
hyperpepsinogenemia 1, 147-48
hyperphagia, 57
hyperplasia: bowel, 306; drug-induced, 510t; focal nodular, 550;
G-cell,
150, 160-62, 163; gastric, 177; in portal
hypertension, 525t
hyperreflexia, 537
hypersalivation, 12-13
hypersecretion, 238t
hypersomnia, 537
hypersplenism, 469
hypertension, 89
hyperthyroidism, 22, 23t, 114t, 234t, 234, 241t,
595
hypertrophic pyloric stenosis, 176
hyperuricosuria, 424-25, 437-38
hypervitaminosis A, 57t
hypoalbuminemia, 25, 325-26, 328, 338, 610
hypocalcemia, 59t, 328
hypochlorhydria, 143, 150, 169t, 169, 431
hypochondriasis, 30
hypogammaglobulinemia, 254
hypogeusia, 208t, 210t
hypoglycemia, 464, 488, 504, 506, 548, 551, 553
hypokalemia, 328, 353t, 431, 506, 539t
hypomagnesemia, 328, 506
hyponatremia, 524, 539t
hypoparathyroidism, 23t, 170, 241t
hypoproteinemia, 243t, 254, 575t
hypoprothrombinemia, 243t, 466t, 467
hyporeflexia, 209t
hypotension, 258, 280, 411
hypothalamus, 15
hypothyroidism, 19t, 20, 114t, 369, 617
hypotonia, 243
hypovolemia, 392, 411, 539t
hypoxia, 538, 539t
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