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219 Cards in this Set
- Front
- Back
the upper and middle respiratory system have traditionally been the domain of ___________ |
otorhinolaryngologists or ear-nose-throat (ENT) specialists |
|
the lower respiratory tract is considered the domain of _________ |
thoracic surgeons and respiratory disease specialists (aka pulmonologists) |
|
what does the upper respiratory tract comprise of? |
the nose, the paranasal sinuses, the pharynx, and the larynx |
|
what is the primary function of the upper respiratory tract? |
to provide entry for inhaled air, thus enabling respiration |
|
a structure included in the respiratory and digestive systems |
pharynx |
|
a highly specialized structure in the neck that also contains vocal cords enabling it to serve as a speech organ |
larynx |
|
a long tube located in the midline of the thorax; gives rise to the right and left main bronchi |
trachea |
|
how many lobes does the right lung have? |
3 |
|
how many lobes does the left lung have? |
2 |
|
pleura covering the outer surface of the lungs |
visceral pleura |
|
covers the inside of the thoracic cage |
parietal pleura |
|
the nasal cavity and the paranasal sinuses are lined by _________ epithelium |
cuboidal |
|
the pharynx and the larynx are lined by ________ epithelium that is identical to the epithelium of the mouth |
squamous |
|
the trachea and the bronchi are lined with ______ epithelium |
cuboidal |
|
alveoli are lined by ________ |
pneumocytes |
|
account for 90% of the alveolar surface; very thin cells designed to allow the passage of air from the alveoli into the blood |
type I pneumocytes |
|
cuboidal cells; specialize in the production of pulmonary surfactant |
type II pneumocytes |
|
an epithelial later that lines both the visceral and parietal pleura |
mesothelium |
|
oxygen and nutrients are brought into the lungs through the _____________ |
bronchial arteries |
|
the inability to produce voice |
aphonia |
|
forms tonsils in the nasopharynx and pharynx and lymphoid follicles in the wall of the bronchi |
MALT (mucosa-associated lymphoid tissue) |
|
acute inflammation involving the nose, paranasal sinuses, throat, or larynx or all of these together; common cold; may extend into trachea or bronchi (pneumonia) |
upper respiratory tract infections (URIs) |
|
most URIs are caused by what? |
viruses |
|
cell infiltrates consist of lymphocytes, macrophages, and plasma cells |
viral URIs |
|
elicit a reaction of polymorphonuclear neutrophils; many present with an exudate |
bacterial infections |
|
used to denote infections of the larynx, trachea, and the major extra pulmonary bronchi; most prevalent among children |
middle respiratory syndrome |
|
examples of middle respiratory syndromes |
croup, epiglottitis, and bronchiolitis |
|
an acute, possibly life-threatening infections that involves the larynx; most common in children younger than 3 years; spasm of the vocal cords |
croup |
|
a sudden loss of voice and hoarseness and throat pain on swallowing; narrowing of air passage; antibiotic treatment or humidified oxygen mask |
epiglottitis |
|
a term used for the acute childhood disease involving the bronchi and bronchioles but not extending into the alveolar spaces of the lungs; viral infection |
bronchiolitis |
|
an inflammation of the lung that occurs in two major forms |
pneumonia |
|
two forms of pneumonia |
alveolar pneumonia and interstitial pneumonia |
|
may be focal or diffuse; marked by intraalveolar inflammation; usually caused by bacteria |
alveolar pneumonia |
|
pneumonia that is limited to the segmental bronchi and surrounding lung parenchyma |
bronchopneumonia |
|
widespread or diffuse alveolar pneumonia; often end result of confluent bronchopneumonia |
lobar pneumonia |
|
usually diffuse and often bilateral; related to infections with Mycoplasma pneumoniae or viruses |
interstitial pneumonia |
|
pneumonias may be classified etiologically as being caused by the following: |
upper respiratory flora, enteric saprophytes, and extraneous pathogens that are not normally associated with the human body |
|
the pathogens responsible for pneumonia can reach the lung parenchyma through several routes including…... |
inhalation of pathogens in air droplets, aspiration of infected secretions from the upper respiratory tract, aspiration of infected particles in gastric contents, food, or drinks, and hematogenous spread |
|
complication of pneumonia; extension of inflammation to the pleural surface commonly leads to pleural effusion; sometimes pus fills the entire pleural cavity; more often it is encapsulated by fibrous tissue into pockets; restrictive lung disease |
pleuritis |
|
complication of pneumonia; usually associated with highly virulent bacteria; cause destruction of the lung parenchyma and suppuration |
abscess |
|
important complication of pneumonia; unresponsive to treatment |
chronic lung disease |
|
a chronic bacterial infectious disease; incidence in the US has decreased steadily since the 1950s; encapsulated bacteria elicit formation of granulomas |
tuberculosis |
|
widespread in the midwestern US; acquired by inhaling dried fungi and their spores; resemble tuberculosis |
histoplasmosis |
|
a localized, destructive, suppurative lesion; may be solitary or multiple; lesions filled with pus |
lung abscess |
|
clinical term used for lung diseases characterized by chronic airway obstruction |
chronic obstructive pulmonary disease (COPD) |
|
excessive production of tracheobronchial mucus causing cough and expectoration for at least 3 months during 2 consecutive years; smoking is the cause in more than 90% of cases |
chronic bronchitis |
|
a permanent dilation of the bronchi; the most common complication of chronic bronchitis |
bronchiectasis |
|
enlargement of the airspaces distal to the terminal bronchioles with destruction of the alveolar walls; no bronchial obstruction; no coughing |
emphysema |
|
immune diseases affecting the respiratory tract |
allergic rhinitis (hay fever), bronchial asthma, sarcoidosis, and hypersensitivity pneumonitis |
|
very common; acute vasomotor response mediated by histamine and related vasoactive substances released locally in the nose from mast cells coated with IgE |
allergic rhinitis (hay fever) |
|
a disease characterized by increased responsiveness of the bronchial tree to a variety of stimuli; wheezing during expiration, cough, and dyspnea |
asthma |
|
mediated by exposure to exogenous allergens and represents a type I hypersensitivity reaction; typically affects children |
extrinsic asthma |
|
precipitated by non immune mechanisms, most of which are nonspecific and would not produce symptoms were it not for the hyper-reactivity of the bronchial tissues |
intrinsic asthma |
|
caused by physical factors (heat or cold), exercise, psychological stress, chemical irritants and air pollution, bronchial infection, and aspirin |
intrinsic asthma |
|
what are the pathologic changes during asthma? |
bronchi show chronic inflammation and overabundance of mucus in the lumen; bronchial gland hyperplasia;elevated IgE and eosinophilia |
|
a multisystemic granulomatous disease of unknown etiology, presumably mediated by cell-mediated immunity; common in blacks; presents granulomas in the lungs, lymph nodes of the thorax and neck, and the liver |
sarcoidosis |
|
an immune disorder caused by repeated inhalation of foreign antigens; aka extrinsic allergic alveolitis |
hypersensitivity pneumonitis |
|
mediated by antibodies that react with the inhaled antigen in the alveoli; dyspnea of sudden onset |
acute pneumonitis |
|
mediated by T lymphocytes and it characterized by a typical cell-mediated reaction; granulomas |
chronic hypersensitivity pneumonitis |
|
lung diseases caused by inhalation of mineral dusts, fumes, and various organic or inorganic particulate matter; most are occupational and are a consequence of long term exposure in the workplace |
pneumoconioses
|
|
severe lung disease; autopsy of patients show black lungs; fibrotic and structurally abnormal lungs |
coal-workers' lung disease (CWLD) |
|
a lung disease caused by inhalation of small silica crystals, which are inhaled in dust generated during stone cutting, mining, and sand blasting; lesions in lung parenchyma |
silicosis |
|
several fibrous silicates that form natural minerals; used in manufacturing and industry for many years; carcinogenic |
asbestos |
|
presents as restrictive lung disease and dyspnea; respiratory failure occurs only rarely |
asbestosis |
|
a clinical term used to describe changes that occur in the lungs under a variety of conditions; causes include shock, pneumonia, toxic lung injury, and aspiration of fluids; lungs are heavy and filled with edema fluid |
acute respiratory distress syndrome (ARDS) |
|
incomplete expansion or, more often, collapse of alveoli; causes include deficiency of surfactant, compression of the lungs from outside, or respiration of air distal to bronchial obstruction |
atelectasis |
|
what are the two most important neoplasms of the respiratory tract |
lung cancer and carcinoma of the larynx |
|
leading cause of cancer death in the U.S. and most other countries; most cases caused by cigarette smoking; very poor prognosis |
lung carcinoma |
|
entry of air into the pleural cavity; typically occurs after stab wounds of the chest wall or rupture of lung tissue |
pneumothorax |
|
accumulation of fluid in the pleural cavity; fluid can be exudate (caused by inflammation) or transudate |
hydrothorax |
|
primary pleural tumor; rare malignant tumor of the pleura; related to exposure to asbestos in the workplace |
mesothelioma |
|
the study of blood |
hematology |
|
a specialized tissue that consists of fluid, known as plasma, and cells, including white blood cells (leukocytes), red blood cells (erythrocytes), and platelets (thrombocytes) |
blood |
|
protein-rich fluid component of the blood, which contains not only albumin and globulins but also all the clotting factors |
plasma |
|
removal of the coagulation proteins transforms plasma into what? |
serum |
|
how much blood does the average person have? |
5.5 - 6 L |
|
what does the buffy coat contain? |
leukocytes and platelets |
|
anemia, leukemia, lymphoma, and bleeding disorders |
hematologic diseases |
|
transport of oxygen from the lungs into the peripheral tissues |
erythrocytes |
|
a complex molecule that consists of four heme groups and four globins |
hemoglobin |
|
characterized by an abnormal B chain |
sickle cell anemia |
|
requires iron, vitamin B12, vitamin B6, and folic acid |
hemoglobin synthesis |
|
red blood cells live in the circulation for _____ days |
120 |
|
short lived cells that survive no more than 4 days in the peripheral circulation |
neutrophils |
|
long-lived blood cells |
monocytes and lymphocytes |
|
the malignancy of circulating white blood cells |
leukemia |
|
a reduction of hemoglobin in red blood cells below normal levels |
anemia |
|
may be a consequence of bone marrow failure or a deficiency of essential nutrients |
decreased hematopoiesis |
|
bone marrow failure |
aplastic anemia |
|
lack of all blood cells |
pancytopenia |
|
old red blood cells are removed from the circulation during their passage through the _______ |
spleen |
|
the most common infectious cause of hemolytic anemia |
malaria |
|
red blood cells appear to be normal; occurs after a massive blood loss; chronic infections and metabolic disease are also a cause |
normocytic, normochromic anemia |
|
red blood cells are small and pale; caused by iron deficiency; seen in thalassemia |
microcytic, hypochromic anemia |
|
a hereditary defect affecting the synthesis of hemoglobin; reduces the rate of glob in chain synthesis; defect is quantitative |
thalassemia |
|
red blood cells are normal in color but are large; typically caused by a deficiency of vitamin B12 and/or folic acid; can also occur in chronic liver disease |
macrocytic, normochronic anemia |
|
a rare but important disease in which anemia is usually accompanied by leukopenia and thrombocytopenia; bone marrow failure |
aplastic anemia |
|
a form of aplastic anemia that is without an identifiable cause; more of these |
idiopathic |
|
a form of aplastic anemia that is related to bone marrow suppression that is caused by cytotoxic drugs, radiation therapy, or viral infection |
secondary |
|
most common form of anemia; associated with a depletion of body iron stores caused by chronic blood loss; hemoglobin synthesis is impeded |
iron deficiency anemia |
|
caused by a deficiency of vitamin B12 or folic acid; delay the normal maturation of blood cells |
megaloblastic anemia |
|
vitamin b12 deficiency; develops as a result of a lack of the gastric intrinsic factor |
pernicious anemia |
|
occur as a result of incased red blood cell destruction (hemolysis) |
hemolytic anemias |
|
caused by a genetic defect in the synthesis of the beta chain of hemoglobin; autosomal recessive gene |
sickle cell anemia |
|
a heterogenous group of genetic defects involving one of several genes encoding the structural proteins that form the cytoskeleton of red blood cells; most common hereditary disease of red blood cells in whites |
hereditary spherocytosis |
|
mediated by antibodies that destroy red blood cells |
immune hemolytic anemia |
|
aka erythrocytosis; denotes an increased number of red blood cells |
polycythemia |
|
a clonal proliferation of hematopoietic stems cells resulting in an uncontrolled production of red blood cells and an increased total red blood cell mass |
primary polycythemia |
|
denotes an increased red blood cell volume as a result of eythroid bone marrow hyperplasia caused by erythropoietin |
secondary polycythemia |
|
a reduction in the white blood cell count to below normal levels; rare |
leukopenia |
|
an increased number of white blood cells in all peripheral blood |
leukocytosis |
|
lymph node enlargement |
lymphadenopathy |
|
increased number of malignant white blood cells in the peripheral blood |
leukemias |
|
bone marrow in infiltrated with malignant cells; peripheral blood contained increased number of immature blood cells; chromosomal or genetic changes; anemia, recurrent infections, and uncontrollable bleeding |
clinical features of leukemia |
|
characterized by massive infiltration of the bone marrow with immature lymphoid cells (blasts) |
acute lymphoblastic leukemia |
|
a heterogenous group of neoplastic diseases characterized by clonal proliferation of myeloblasts in the bone marrow and their entry into the blood or other tissues |
atue myelogenous leukemia |
|
a malignant disease of pluripotent hematopoietic stem cells capable of differentiating into neutrophilic leukocytes |
chronic myelogenous leukemia |
|
a malignant disease involving lymphoid cells; disease of older people |
chronic lymphocytic leukemia |
|
a term that can be applied to an entire spectrum of malignant diseases involving lymphocytes and their precursors |
lymphoma |
|
all lymphomas are malignant true or false |
TRUE |
|
a technique in which labeled antibodies are used to analyze the tissues for the presence of specific tumor cells |
immunohistochemistry |
|
a technique for sorting cells according to their surface properties; biopsied lymph nodes is dispersed into a single-cell suspension and then stained with monoclonal antibodies to specific surface antigens known as clusters of differentiation |
flow cytometry |
|
based on the karyotyping of tumor cells |
cytogenic analysis |
|
lymph node enlargement, fatigue, fever, weight loss, sweating, tumor spread |
symptoms of non hodgkin's lymphoma |
|
the most common form of lymphoma is the US; 45% of all cases; mostly in older people; slow-growing tumor |
follicular lymphoma |
|
occur in several forms; most common aggressive form of NHL |
diffuse large B cell lymphomas |
|
highly malignant tumor composed of small B cells that divide rapidly |
burkitt's lymphoma |
|
a form of malignant disease that is pathologically distinct from other lymphomas; affects all age groups; 5 types |
hodgkin's lymphoma |
|
a malignant disease of plasma cells |
multiple myeloma |
|
the process that prevents uncontrolled bleeding |
hemostasis |
|
develops as a result of decreased production or increased destruction, removal, or utilization of platelets |
thrombocytopenia |
|
important causes of acquired clotting factor deficiencies |
anticoagulants |
|
another name for the normal gastrointestinal tract |
alimentary or digestive tract |
|
the upper tract |
mouth, pharynx, esophagus, stomach, and duodenum |
|
the lower tract |
the small and large intestine, appendix, rectum, and anus |
|
four layers of the gastrointestinal tract |
1.) mucosa 2.) submucosa 3.) muscularis 4.) serosa (or adventitia) |
|
a serosal surface that covers the outer surface of the stomach and the intestines |
peritoneum |
|
covers the organs |
visceral peritoneum |
|
covers the rest of the abdominal cavity |
parietal peritoneum |
|
what provides blood to most of the abdominal organs |
upper and lower mesenteric arteries |
|
the foregut gives rise to what? |
pharynx, esophagus, and stomach, as well as the respiratory tract |
|
the midgut gives rise to what? |
small intestines |
|
the hindgut gives rise to what? |
the colon |
|
what is the main function of the GI tract |
the digestion of food and alimentation |
|
what are the phases of digestion? |
1.) ingestion 2.) mastication 3.) deglutition (swallowing) 4.) digestion 5.) absorption 6.) excretion |
|
an abnormality in the innervation of the rectum and the sigmoid colon |
Hirschsprung's disease |
|
infection that causes severe watery diarrhea caused by ingestion |
cholera |
|
abnormal or strained swallowing |
dysphagia
|
|
vomiting of blood |
hematemesis |
|
bleeding from the rectum |
hematochezia |
|
produced by the adenocarcinomas of the intestine; can be measured in the serum of adult patients; a valuable tumor marker |
carcinoembryonic antigen (CEA) |
|
a congenital abnormality that occurs with increased frequency in some families; inherited as a polygenic trait |
cleft lip |
|
inflammation of the oral mucosa |
stomatitis |
|
one of the most common diseases in humans; a multifactoral disease mediated by oral saprophytic bacteria; "dry rot" |
dental caries |
|
a common disorder accounting for more tooth loss than caries and all other dental diseases combines; tartar; swollen and tender gums; pus |
periodontal disease |
|
common and may involve the lips, tongue, soft palate, etc.; complication of smoking and chewing tobacco; chronic alcoholism |
oral cancer |
|
three major salivary glands |
parotid, the submandibular, and the sublingual |
|
inflammation of the salivary glands |
sialadenitis |
|
overproduction of saliva |
sialorrhea |
|
dry mouth |
xerostomia |
|
periductal fibrosis or ductal stone |
sialolithiasis |
|
xerophthalmia |
dry eyes |
|
most common histologic tumor type; benign and composed of epithelial and myo-epithelial cells and areas resembling cartilage |
pleomorphic adenoma |
|
lack of lumen; an abnormality that presents shortly after birth and is often associated with abnormal connections between the esophagus and trachea |
congenital atresia |
|
leads to displacement of the cardiac portion of the stomach from the abdominal cavity into the thoracic cavity |
hiatal hernia |
|
"lack of relaxation"; antithesis of LES insufficiency; spasm of the LES; dilation of the esophagus proximal to the site of the spasm; inability to swallow food |
achalasia |
|
inflammation of the esophagus; may be caused by infection, reflux of gastric juice, or exogenous irritants, chemicals, and drugs |
esophagitis |
|
a risk factor for cancer; mucosa of esophagus is more sensitive to injury than normal squamous epithelium and may give rise to peptic ulcers |
Barrett's esophagus |
|
most important neoplasm of the esophagus; malignant lesion; unfavorable prognosis |
carcinoma of the esophagus |
|
a chronic multifactoral disease characterized by muscosal ulceration that extends through the entire gastric epithelial later and into the muscularis |
peptic ulcer |
|
etiology of a peptic ulcer |
gastric juice, mucosal barrier, or h. pylori infection |
|
accounts for 90% of all malignant tumors in the stomach; incidence has decreased in the US |
carcinoma of the stomach |
|
disease characterized by the formation of diverticula (outpouchings of the intestinal wall) |
diverticulosis |
|
varicosites of the anal and peri anal region that affect approximately 5% of all adults |
hemorrhoids |
|
a localized vascular lesion of the colon that may cause unexplained bleeding in elderly persons |
angiodysplasia of the intestines |
|
includes several disorders that compromise blood flow through segments of the intestine |
ischemic bowel disease |
|
a term used for two closely related but distinct diseases (Crohn's disease and ulcerative colitis); recurrent inflammation of the intestines and a chronic, unpredictable course |
inflammatory bowel disease (IBD) |
|
a chronic inflammation of the gastrointestinal tract that most often involved the terminal ileum and the colon |
crohn's disease |
|
most common symptoms of crohn's disease |
diarrhea, abdominal pain, and weight loss |
|
an intestinal inflammation of unknown etiology that most often involves the large intestine |
ulcerative colitis |
|
an acute infectious disease marked by the formation of pseudomembranes on the surface of the intestinal mucosa; predominantly involves the colon ; caused by C. difficult |
pseudomembranous colitis |
|
a common cause of viral gastroenteritis in infants and children; virus destroys mucosal cells of the small intestine; watery diarrhea |
rotavirus |
|
a common cause of acute viral gastroenteritis in children and adults; occasionally epidemics occur in nursing homes or cruise ships; extremely infectious |
norovirus |
|
caused by enterogenic bacteria of the normal intestinal flora that become pathogenic after an obstruction of the lumen of the appendix; swollen and inflamed appendix; rupture could be life threatening |
appendicitis |
|
symptoms of acute appendicitis |
sudden fever, leukocytosis, and abdominal pain |
|
an inflammation of the peritoneal lining of the abdominal cavity; can be localized or diffuse; classified as infectious or sterile |
peritonitis |
|
a protrusion of the abdominal contents through the abdominal wall; relate to a weakness or a defect in the abdominal wall |
hernia |
|
the most common hernia |
inguinal hernia |
|
an invagination of one segment of the intestine into another |
intussusception |
|
a rotation of the intestine around it's mesenteric attachment site |
volvulus |
|
aka gluten-sensitive enteropathy; intestinal disease characterized by hypersensitivity to gliadin in dietary grains; genetic predisposition |
celiac sprue |
|
caused by bacteria that typically affect visitors to the tropics; morphologic changes in the intestine; more pronounced distally; antibiotic treatment |
tropical sprue |
|
a malabsorption caused by tropheryma whippelii, a bacterium that invades the small intestinal mucosa; middle-aged men; familial clustering; antibiotics |
while's disease |
|
rare autosomal dominant diseases; colon shows multiple adenomas with evolve into adenocarcinomas; hereditary |
familial adenomatous polyposis coli (FAP) |
|
used for neuroendocrine tumors of low malignancy, meaning that they are malignant but not as malignant as true carcinomas |
carcinoid |
|
the largest parenchymal organ in the body |
the liver |
|
located in the right upper abdominal quadrant |
liver |
|
main excretory product of the liver; complex mixture of bilirubin, bile salts, lipids, and many other major and minor components; stored in gallbladder |
bile |
|
abnormal formation, processing, or excretion of bilirubin |
jaundice syndromes |
|
inflammation of the liver; can be caused by viruses, as well as drugs, alcohol, and immune mechanisms |
hepatitis |
|
liver cells may be injured by exogenous chemicals or endogenous metabolites |
toxic/metabolic hepatic injury |
|
this condition may result from a variety of liver disease; the term is used as a synonym for end-stage liver disease |
cirrhosis |
|
most prevalent liver disease in the world; clinical syndrome of variable severity caused by one of several hepatotropic viruses; A, B, C, D, and E |
acute viral hepatitis |
|
transmitted by fecal-oral route and may occur is sporadic or epidemic form; sources are sewage, contaminated food, drinks, and shellfish; most prevalent among children in underdeveloped countries; mild fever with vomiting, loss of appetite, and jaundice |
hepatitis A |
|
an encapsulated DNA virus that is specific specific for humans and higher primates; symptoms appear 40-180 days after infection; follows after transfusion of blood, exposure to contaminated blood, or sexual contact |
hepatitis B |
|
an incomplete RNA virus that requires HBV for its own repletion; infection with these two viruses can occur simultaneously |
hepatitis D |
|
a flavivirus; an RNA virus of variable size that encodes a single polypeptide; antibodies are used to diagnose infection; most often acquired by blood contaminating the needles during intravenous drug abuse; multiple sex parters, surgery, accidental needle stick |
hepatitis C |
|
an RNA virus transmitted by fecal-oral route; endemic in parts of Asia, Africa, and South America and Mexico; cause waterborne endemics; usually asymptomatic or mild; heals without serious consequences |
hepatitis E |
|
fatty liver in obese persons, persons with diabetes, and occasionally even without any obvious causes |
steatohepatitis |
|
an autosomal dominant disorder of bilirubin metabolism that affects about 5% of the total population; disease causes intermittent jaundice that usually begins after puberty and most common in male subjects |
gilbert's disease |
|
an autosomal recessive defect of iron absorption that results in excessive accumulation of iron in the liver and several other organs; damages liver cells and induces cirrhosis |
hereditary hemochromatosis |
|
aka hepatolenticular degeneration; autosomal recessive disorder of copper metabolism that produces lesions in the liver, brain, and eye |
wilson's disease |
|
an autosomal recessive disorder that is related to the presence of the PiZ allele of the gene that encodes for AAT |
alpha-antitrypsin deficiency (AAT) |
|
a form of chronic hepatitis; thought to be immune mediated because it is associated with other autoimmune phenomena; affects young women |
autoimmune hepatitis |
|
a disease of unknown etiology that is characterized by destruction of intrahepatic bile ducts and progression to cirrhosis |
primary biliary cirrhosis |
|
a disease of unknown origin that also may have an immune pathogenesis; primarily affects adult men younger than 40 years |
primary sclerosing cholangitis |
|
liver is resistant to ______ infections |
bacterial |
|
concretions composed of chemicals normally formed in bile; extremely common and in the US more than half a million people undergo surgery for these a year |
gallstones |
|
two types of gallstones |
cholesterol stones and pigmentary stones |