i-m

Immune reconstitution inflammatory syndrome (IRIS): A paradoxical clinical worsening of a known infection or the appearance of a new condition after initiating antiretroviral therapy in HIV-infected patients (or recovery from immunosuppression in non-HIV infected patients).

Immunoassay: A blood test for antibodies to antigens that worsen asthma, such as pollen, mold, or dust mites.

Immunogenicity: Ability of a substance to provoke an immune

response.

Immunoglobulin G index: The ratio of immunoglobulin G to

protein in the serum or cerebrospinal fluid.

Immunophenotyping: A process used to identify cells, based on the types of antigens or markers on the surface of the cell. This process is used to diagnose specific types of leukemia and lymphoma by comparing the cancer cells to normal cells of the immune system.

Immunotherapy: A type of biological therapy that uses substances to stimulate or suppress the immune system to help the body fight cancer, infection, and other diseases.

Implantable cardioverter-defibrillator: A device implanted into the heart transvenously with a generator implanted subcutaneously in the pectoral area that provides internal electrical cardioversion of ventricular tachycardia

or

defibrillation of ventricular fibrillation.Incretin effect: A greater insulin stimulatory effect after an oral glucose load than that caused by an intravenous glucose infusion. The majority of the effect is thought to be due to glucose-dependent insulinotropic peptide (GIP) and glucagon like peptide-1 (GLP-1). Patients with type 2 diabetes have a significant reduction of the incretin effect, implying that these patients either have decreased concentration of the incretin hormones, or a resistance to their effects. GLP-1 concentrations are reduced in patients with type 2 diabetes in response to a meal, while GIP concentrations are either normal or increased, suggesting a resistance to the actions of GIP, thus making GLP-1 a more logical target for therapeutic intervention.

Induction: The first treatment given for a disease. It is often part of a standard set of treatments, such as surgery followed by chemotherapy and radiation.

Infantile spasms (West syndrome): A seizure syndrome in infants younger than 1 year. It is characterized by a specific electroencephalogram pattern and spasms or jitters.

Inotropic: Relating to or influencing the force of muscular

contractions.

In-stent restenosis:

Complex process following stent

implantation resulting in smooth muscle cell proliferation within an implanted stent, renarrowing of the arterial lumen, and recurrent ischemia.Insulin resistance: A decreased response to insulin found before or early in the diagnosis of type 2 diabetes mellitus.

International normalized ratio (INR): The ratio of the patient's clotting time to the clinical laboratory's mean reference value; normalized by raising it to the international sensitivity index (ISI) power to account for differences in thromboplastin

reagents. Therefore, INR = (patient's prothrombin time/

laboratory's mean normal prothrombin time)iS!.

Interstitial nephritis: An acute inflammation of the kidney, often due to drugs; patients commonly present with fever, rash, and peripheral eosinophilia.

Intraabdominal: Within the abdominal cavity.

Intraarticular: Administered to or occurring in the space within joints.

Intraperitoneal: Within the peritoneal cavity.

Intravesicular: Situated or occurring within the bladder.

Intussusception: The prolapse of part of the intestine into the

lumen of an immediately adjoining part. Blood supply to the

telescoped region can be compromised leading to necrosis.

Iontophoresis: Introduction of a medication into tissue through

use of an electric current.

Ipsilateral: Occurring on the same side.

Ischemia: Deficient supply of blood to a part(s) of the body.

Ischemic penumbra: Ischemic but still viable cerebral tissue.

Typically a rim of mild to moderately ischemic tissue in

between normally perfused tissue and the area of evolving

infarction; may remain viable for several hours.

synuclein inside some nerve cells.

Jejunal entercocyte: Cells lining the jejunum, a section of the

small intestine connecting the duodenum to the ileum.

Jejunostomy: Operative placement of a new opening into the

Jugular venous distention: Assessed with the patient laying at a

Juvenile myoclonic epilepsy: An epilepsy syndrome that typically

Keratinization: The sloughing of epithelial cells in the hair follicle.

Keratinocytes: The predominant cell type in the outermost layer

Lesch–Nyhan syndrome: A rare inherited gene mutation that

results in accumulation of abnormally high uric acid levels.

Leukocytoclastic vasculitis: Acute cutaneous vasculitis

characterized by purpura (especially of the legs) and

histologically by exudation of neutrophils and sometimes fibrin

around dermal venules, with extravasation of red blood cells.

Leukopenia: A condition where the number of circulating white

blood cells are abnormally low due to decreased production of

new cells, possibly in conjunction with medication toxicities.

Lewy bodies: Abnormal deposits of a protein called alpha-

Lhermitte sign: Tingling or shock-like sensation passing down

the arms or trunk when the neck is flexed.

Libido: Sexual drive or desire.

jejunum, usually associated with feeding tube placement.

Ligament of Treitz: Landmark in the proximal portion of the

jejunum beyond which it is preferred that postpyloric feedings

45 degree angle, and demonstrating a measurement of the right

be delivered to minimize aspiration.

internal jugular vein that is more than 4 cm above the sternal

Linea nigra: Dark vertical line that appears on the abdomen

angle; suggests systemic venous congestion and volume overload.

during pregnancy.

Linear accelerator: A device in which charged particles are

occurs during teenage years and consists of generalized tonic-

accelerated in a straight line by successive impulses from a

seizures and myoclonic jerks. Absence seizures may also occur

series of electric fields.

with this syndrome.

Lipophilic: Having affinity for fatty substances.

Lipoprotein lipase: Enzyme located in the capillary endothelium

involved in the breakdown of intravenous lipid emulsion

of the skin.

particles.

Keratitis: Infection of the cornea.

Livedo reticularis: Purple mottling of the skin.

Keratoconjunctivitis sicca: An eye disease caused by eye dryness,

Lower esophageal sphincter: A manometrically defined zone

which results from either decreased tear production or increased

of the distal esophagus with an elevated basal resting pressure

tear film evaporation. Also known as dry eye syndrome.

that prevents the reflux of gastric material from the stomach.

Kernicterus: Form of brain damage caused by excessive jaundice.

It relaxes on swallowing to permit the free passage of food into

Ketosis: An abnormal increase of ketone bodies present in

the stomach.

conditions of reduced or disturbed carbohydrate metabolism.

Lymphangitis: Inflammation of lymphatic channels.

Korotkoff sounds: The noise heard over an artery by auscultation

Lymphatic: The network of vessels carrying tissue fluids.

when pressure over the artery is reduced below the systolic

Lymphedema: Swelling, primarily in the appendages, caused by a

arterial pressure.

blockage or disruption in the lymphatic system.

Kyphosis: Abnormal curvature of the spine resulting in protrusion

Lymphoproliferative: Of or related to the growth of lymphoid

of the upper back; hunchback.

tissue.

Lactose intolerance: The inability to digest lactose, a sugar found

Magnetic resonance imaging: A form of medical imaging that

in milk products, resulting in diarrhea, bloating, and gas after

measures the response of the atomic nuclei of body tissues to

ingestion.

high-frequency radio waves when placed in a strong magnetic

Lagophthalmos: Poor closure of the upper eyelid.

field, and that produces images of the internal organs.

Lamina cribrosa: A series of perforated sheets of connective

Major malformation: A defect that has either cosmetic or

tissue that the optic nerve passes through as it exits the eye.

functional significance to the patient.

Laminectomy: A surgical operation to remove the back of one or

Maltodextrin: Easily digestible partially hydrolyzed starch.

more vertebrae.

Marcocytosis: Enlargement of red blood cells with near-constant

Laparoscopic: Abdominal exploration or surgery employing a

hemoglobin concentration.

type of endoscope called laparoscope.

Mastalgia: Tenderness of the breasts.

Laparoscopic adjustable gastric banding: A surgical procedure

Mastodynia: Pain in the breast.

for weight loss that elicits its effectiveness through gastric

Matrix metalloproteinases: Any of a group of enzymes, normally

volume limitation. The procedure involves inserting a silicone

located in the extracellular space of tissue, that function to

band lined with an inflatable donut-shaped balloon around the

break down proteins (eg, collagen) and require zinc or calcium

neck of the stomach to be filled with isotonic liquid.

atoms as cofactors for enzymatic activity. Responsible for the

Laparotomy: Surgical opening of the abdominal cavity.

degradation of connective tissue.

Left shift: An increase in the number of immature neutrophils

Meatal stenosis: Narrowing in the opening of the urethra.

(also referred to as bands). A left shift usually indicates infection

Meconium: First intestinal discharge (“stool”) of a newborn

or inflammation. The term originated in the days in which lab

infant, usually green in color and consisting of epithelial cells,

reports were written by hand and the bands were written on the

mucus, and bile.

left-hand side of the lab report. Also known as bandemia.

Medication-assisted treatment: The use of medications with

Lennox–Gastaut syndrome: An epilepsy syndrome

counseling and other behavioral therapies for the treatment of

that often appears early in life that consists of a distinct

substance use disorders.

electroencephalogram pattern, mild to severe developmental

Melasma: Patchy skin pigmentation or dark skin discoloration,

delay, and multiple seizure types.

often seen during pregnancy

Melena: Abnormally dark black, tarry feces containing blood

(usually from gastrointestinal bleeding).

Menarche: The first menstrual cycle.

Meninges: Membranes surrounding the brain and spinal cord.

Meningismus: Symptoms similar to meningitis (nuchal rigidity,

photophobia, and headache) but not caused by meningitis.

Mesial temporal lobe epilepsy: A common epilepsy syndrome

manifested by seizures arising from the mesial temporal lobe

of the brain, and is often associated with an anatomical change,

described as hippocampal sclerosis.

Mesocortical pathway: A neural pathway that connects the

ventral tegmentum to the cortex, particularly the frontal lobes.

It is one of the major dopamine pathways in the brain.

Mesothelioma: A benign or malignant tumor affecting the lining

of the chest or abdomen. Commonly caused by exposure to

asbestos fibers.

Metabolic acidosis: A condition in the blood and tissues that

is a consequence of an accumulation of lactic acid resulting

from tissue hypoxia and anaerobic metabolism. It may also

be caused by a decrease in the concentration of alkaline

compounds (typically bicarbonate).

Metabolic syndrome: Constellation of cardiovascular risk factors

related to hypertension, abdominal obesity, dyslipidemia,

and insulin resistance diagnosed by the presence of at least

three of the following criteria: increased waist circumference,

elevated triglyceride concentrations, decreased high density

lipoprotein (HDL) cholesterol or active treatment to raise HDL

cholesterol, elevated blood pressure or active treatment with

antihypertensive therapy, or elevated fasting glucose or active

treatment for diabetes.

Metastasis: Cancer that has spread from the original site of the

tumor.

Methemoglobinemia: A condition caused by elevated levels

of methemoglobin in red blood cells, resulting in enhanced

oxygen affinity in heme sites and reduced oxygen delivery to

tissues; leads to hypoxia, cyanosis, shortness of breath, mental

status changes, and dizziness. In severe cases, it can lead to

seizures, coma, or death.

Microalbuminuria: Urinary excretion of small but abnormal

amounts of albumin. Confirmed spot urine albumin to

creatinine ratio of 30 to 300 mg/g (3.4–34 mg/mmol creatinine)

is consistent with microalbuminuria. Considered an early sign

of chronic kidney disease.

Microcytosis: A condition in which the erythrocytes are smaller

than normal.

Micrognathia: Abnormal smallness of the jaws.

Micrographia: Small handwriting.

Microsatellite instability (MSI): The condition of genetic

hypermutability that results from impaired DNA mismatch

repair (MMR). The presence of MSI represents phenotypic

evidence that MMR is not functioning normally.

Microvascular: Pertaining to the smaller vessels of the circulatory

system such as capillaries, venules, and arterioles.

Microvascular pulmonary emboli: An obstruction in the small

blood vessels in the lung caused by material (eg, blood clot, fat,

air, foreign body) that is carried through the circulation until it

lodges in another small vessel.

Micturition: Act of passing urine.

Minimum inhibitory concentration: The lowest concentration

of a drug that visually inhibits the growth of a microorganism.

Minor malformation: Defect that has neither cosmetic nor

functional significance to the patient.

APPENDIX C | GLOSSARY 1585

Mixed mood features: Symptoms of mania and depression

occurring simultaneously or in close juxtaposition. Criteria

are either met for a manic/hypomanic episode and there are

also at least three symptoms of depression, or criteria are met

for a depressive episode with at least three manic/hypomanic

symptoms.

Mobilization: A process by which medication(s) are used to

promote the release of hematopoietic stem cells from the

bone marrow to the peripheral blood for the purpose of

collecting a sufficient amount of hematopoietic stem cells for

a hematopoietic stem cell transplant.

Moebius syndrome: Rare congenital neurological disorder

which is characterized by facial paralysis and affects eye

movement.

Monoamine neurotransmitters: Serotonin, norepinephrine,

dopamine.

Monoparesis: Slight or incomplete paralysis affecting a single

extremity or part of one.

Monosodium urate: A crystallized form of uric acid that can

deposit in joints leading to an inflammatory reaction and the

signs and symptoms of gout.

Morphology: Structure and form of a cell.

Mucositis: Inflammatory, erosive, and/or ulcerative process

inside the mouth, which is usually caused by radiation or

chemotherapy.

Multiparity: Condition of having given birth to multiple children.

Muscularis mucosa: The thin layer of smooth muscle found in

most parts of the gastrointestinal tract.

Mydriasis: Pupil dilation.

Myelin: A protein and phospholipid sheath that surrounds the

axons of certain neurons. Myelinated nerves conduct impulses

more rapidly than nonmyelinated nerves.

Myeloablative preparative regimen: Chemotherapy regimens

with or without radiation that cause irreversible cytopenias

without hematopoietic stem cell support.

Myelodysplastic syndrome: A type of cancer in which the bone

marrow does not make enough healthy blood cells (white

blood cells, red blood cells, and platelets) and there are

abnormal cells in the blood and/or bone marrow.

Myelopathy: A neurologic deficit related to the spinal cord.

Myelosuppression: Reduction in white blood cells, red blood

cells, and platelets.

Myocardial infarction: The formation of an infarct, an area of

tissue death, due to a local lack of oxygen. Myocardial cell

death secondary to prolonged ischemia.

Myocarditis: Inflammation of the heart muscle.

Myoglobinuria: The presence of myoglobin in urine.

Myonecrosis: Necrotic damage to muscle tissue.

Myopathy: Any disease of the muscle causing weakness, pain,

and tenderness.

Myringotomy: A surgical incision made in the tympanic

membrane to relieve pressure and drain fluid from the

middle ear.

Myxedema: Hypothyroidism characterized by a relatively hard

edema of subcutaneous tissue, with increased content of

proteoglycans in the fluid; characterized by somnolence, slow

mentation, dryness and loss of hair, increased fluid in body

cavities such as the pericardial sac, subnormal temperature,

hoarseness, muscle weakness, and slow return of a muscle to

the neutral position after a tendon jerk.