Chronic and Acute Diseases
questions & 100% verified answers
Aspiration pneumonitis - ANSWER a condition caused by the
abnormal entry of fluids, particulate matter, or secretions into the lower
airways that can lead to chemical pneumonitis from entry of toxic
material such as gastric acid, from bacterial infection, or by mechanical
obstruction of the lower airways.
Asthma - ANSWER a chronic inflammatory disorder of the airways
involving bronchial hyperresponsiveness and airway obstruction marked
by periodic attacks of wheezing, shortness of breath, a tight feeling in
the chest, and a cough that produces mucus because of an allergic
reaction triggered by certain drugs, irritants, viral infection, exercise, or
emotional stress.
Asymptomatic bacteriuria - ANSWER the presence of bacteria in the
urine without evidence of infection.
Ataxia-telangiectasia (AT) - ANSWER see Immune deficiency.
Ataxic cerebral palsy - ANSWER a form of cerebral palsy associated
with damage to the cerebellum and resulting in gait disturbances and
instability; at birth the infant may have hypotonia, but develops stiffness
of the trunk muscles later in infancy.
, Atelectasis - ANSWER part of or an entire lung collapses and the
alveoli deflate as a result of surgery, smoking, or blockage of a
bronchiole.
Absorption atelectasis - ANSWER collapse of lung tissue resulting
from gradual absorption of air from obstructed or hypoventilated alveoli
or from inhalation of concentrated oxygen or anesthetic agents.
Compression atelectasis - ANSWER air pressure in the pleural space
pushes against the already recoiled lung, causing compression
atelectasis, and against the mediastinum, compressing and displacing the
heart and great vessels.
Surfactant impairment - ANSWER decreased production or
inactivation of surfactant, which is necessary to reduce surface tension in
the alveoli and causes lung collapse during expiration; can occur
because of premature birth, acute respiratory distress syndrome,
anesthesia, or mechanical ventilation.
Atherosclerosis - ANSWER a type of arteriosclerosis in which the
inflammatory changes of thickening and hardening of the walls of large-
and medium-sized arteries are caused by an atheroma or plaque of lipids,
cells, and connective tissue in the tunica intima.
Atopic dermatitis (AD) (allergic dermatitis) - ANSWER a chronic
hereditary skin disease characterized by intense itching and inflamed
skin that causes redness, swelling, cracking, crusting, and scaling.
, Atrial septal defect (ASD) - ANSWER a congenital heart disease
involving the interatrial septum of the heart that separates the right and
left atria, which results in misdirected blood flow between the two sides
of the heart.
Atrioventricular canal (AVC) defect - ANSWER a large hole is present
in the center of the heart where the wall between the atria joins the wall
between the ventricles, and the tricuspid and mitral valves are formed
into a single large valve that crosses the defect.
Atypical ductal hyperplasia (ADH) - ANSWER abnormal proliferating
cells in breast ducts.
Atypical hyperplasia - ANSWER increased number of cells with some
variation in cellular structure but without sufficient qualitative or
quantitative features of carcinoma.
Atypical lobular hyperplasia (ALH) - ANSWER abnormal proliferating
cells in breast lobules.
Autoimmune hemolytic anemia (AIHA) - ANSWER see Anemia.
Autoimmune neonatal thrombocytopenia - ANSWER see
Thrombocytopenia.
, Autoimmune vascular purpura (allergic purpura) - ANSWER purpura
caused by antibody-mediated injury of blood vessel walls, typically
arterioles and capillaries. The reaction is directed to foreign proteins or
chemicals in the blood (microorganisms, drugs, or other chemicals) that
deposit on the vessel walls.
Autonomic hyperreflexia (dysreflexia) - ANSWER a syndrome
resulting from afferent stimuli that cause intense sympathetic discharge
originating with spinal cord injury above the major splanchnic outflow;
characterized by hypertension, bradycardia, sweating of the forehead,
severe headache, and piloerection on distention of the bladder and
rectum.
Autosomal agammaglobulinemia - ANSWER see Immune deficiency.
Autosomal dominant polycystic kidney disease (ADPKD) - ANSWER
a progressive disease characterized by formation of multiple cysts of
varying size scattered diffusely throughout both kidneys, resulting in
compression and destruction of renal parenchyma, usually with
hypertension, gross hematuria, and uremia leading to progressive renal
failure.
Autosomal hyper-IgM syndrome - ANSWER see Immune deficiency.
Azotemia - ANSWER kidney dysfunction characterized by increased
serum urea levels and frequently associated with increased creatinine
levels.